e424b5
Filed
Pursuant to Rule 424(b)(5)
Registration No. 333-170105
(to Prospectus dated November 15, 2010)
2,750,000 Shares
Common Stock
We are selling 2,750,000 shares of our common stock.
Our shares trade on The NASDAQ Global Select Market under the
symbol RDEA. On January 19, 2011, the last sale
price of the shares as reported on The NASDAQ Global Select
Market was $26.81 per share.
As part of this offering, the underwriters are selling an
aggregate of 577,400 shares of our common stock to entities
affiliated with two of our directors and principal stockholders
at the public offering price.
Investing in the common stock involves risks that are
described in the Risk Factors section on
page S-7
of this prospectus supplement.
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Proceeds,
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Price to
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Underwriting
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Before Expenses,
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Public
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Discount(1)
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to Us(1)
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Per share
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$26.00
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$1.56
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$24.44
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Total
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$71,500,000
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$3,389,256
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$68,110,744
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(1)
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The underwriters will not receive any underwriting discount on
the sale of an aggregate of 577,400 shares of our common
stock to entities affiliated with two of our directors and
principal stockholders.
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The underwriters may also exercise their option to purchase up
to an additional 412,500 shares from us, at the public
offering price, less the underwriting discount, for 30 days
after the date of this prospectus supplement to cover
overallotments, if any.
Neither the Securities and Exchange Commission nor any state
securities commission has approved or disapproved of these
securities or determined if this prospectus supplement or the
accompanying prospectus is truthful or complete. Any
representation to the contrary is a criminal offense.
The shares will be ready for delivery on or about
January 25, 2011.
Joint Book-Running Managers
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BofA
Merrill Lynch |
Jefferies |
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JMP
Securities |
Brean Murray, Carret & Co. |
Roth Capital Partners |
The date of this prospectus supplement is January 20, 2011.
Table of
Contents
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Prospectus Supplement
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S-ii
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S-1
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S-7
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S-8
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S-9
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S-10
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S-11
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S-17
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S-17
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S-17
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S-17
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Prospectus
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We have not authorized anyone to provide any information
other than that contained or incorporated by reference in this
prospectus supplement or the accompanying prospectus or in any
free writing prospectus prepared by or on behalf of us that we
have authorized for use in connection with this offering. We
have not, and the underwriters have not, authorized anyone to
provide you with different information. We and the underwriters
take no responsibility for, and can provide no assurance as to
the reliability of, any other information that others may give
you. We are not, and the underwriters are not, making an offer
to sell these securities in any jurisdiction where the offer or
sale is not permitted. You should assume that the information
appearing in this prospectus supplement, the accompanying
prospectus, the documents incorporated by reference in this
prospectus supplement and the accompanying prospectus, and in
any free writing prospectus prepared by or on behalf of us that
we have authorized for use in connection with this offering is
accurate only as of the date of those respective documents. Our
business, financial condition, results of operations and
prospects may have changed since those dates. You should read
this prospectus supplement, the accompanying prospectus, the
documents incorporated by reference in this prospectus
supplement and the accompanying prospectus, and any free writing
prospectus prepared by or on behalf of us that we have
authorized for use in connection with this offering, in their
entirety before making an investment decision. You should also
read and consider the information in the documents we have
referred you to in the sections of this prospectus supplement
entitled Where You Can Find More Information and
Information Incorporated by Reference.
S-i
ABOUT
THIS PROSPECTUS SUPPLEMENT
This document is in two parts. The first part is this prospectus
supplement, which describes the terms of this offering of common
stock and also adds to and updates information contained in the
accompanying prospectus and the documents incorporated by
reference into this prospectus supplement and the accompanying
prospectus. The second part, the accompanying prospectus dated
November 15, 2010, including the documents incorporated by
reference therein, provides more general information. Generally,
when we refer to this prospectus, we are referring to both parts
of this document combined. To the extent there is a conflict
between the information contained in this prospectus supplement,
on the one hand, and the information contained in the
accompanying prospectus or in any document incorporated by
reference that was filed with the Securities and Exchange
Commission, or SEC, before the date of this prospectus
supplement, on the other hand, you should rely on the
information in this prospectus supplement. If any statement in
one of these documents is inconsistent with a statement in
another document having a later datefor example, a
document incorporated by reference in the accompanying
prospectusthe statement in the document having the later
date modifies or supersedes the earlier statement.
All references in this prospectus supplement and the
accompanying prospectus to Ardea, RDEA,
the Company, we, us,
our, or similar references refer to Ardea
Biosciences, Inc., and its whollyowned subsidiary, except where
the context otherwise requires or as otherwise indicated.
This prospectus supplement, the accompanying prospectus and the
information incorporated herein and therein by reference include
trademarks, service marks and trade names owned by us or other
companies. All trademarks, service marks and trade names
included or incorporated by reference into this prospectus
supplement or the accompanying prospectus are the property of
their respective owners.
S-ii
SUMMARY
This summary highlights certain information about us, this
offering and selected information contained elsewhere in or
incorporated by reference into this prospectus supplement. This
summary is not complete and does not contain all of the
information that you should consider before deciding whether to
invest in our common stock. For a more complete understanding of
our company and this offering, you should read and consider
carefully the more detailed information in this prospectus
supplement and the accompanying prospectus, including the
information incorporated by reference in this prospectus
supplement and the accompanying prospectus, and the information
included in any free writing prospectus that we have authorized
for use in connection with this offering. If you invest in our
common stock, you are assuming a high degree of risk. See
Risk Factors in this prospectus supplement beginning
on
page S-7
and in the documents incorporated by reference into this
prospectus supplement.
Overview
We are a biotechnology company focused on the development of
small-molecule therapeutics for the treatment of serious
diseases. The current status of our development programs is as
follows:
Product
Portfolio
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Product Candidate
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Target Indication
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Development Status
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RDEA594
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Gout
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Phase 2 completed
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Next-generation URAT1 inhibitors
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Gout
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Preclinical development ongoing
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BAY 86-9766
(formerly known as RDEA119)
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Cancer
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Phase 2 ongoing
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Gout
Gout is a painful, debilitating and progressive disease. While
gout is a treatable condition, there are limited treatment
options, and a number of adverse effects are associated with
most current therapies.
Gout is caused by abnormally elevated levels of uric acid in the
blood stream. Drugs currently used to treat the underlying cause
of gout work by lowering blood or serum uric acid
(sUA) levels. Approximately 90 percent of gout
patients are considered to have a defect in their ability to
excrete sufficient amounts of uric acid and are classified as
under-excreters of uric acid, which leads to
excessive levels of uric acid in the blood stream. Our most
advanced product candidate, RDEA594, is an inhibitor of URAT1, a
transporter in the kidney that regulates uric acid excretion
from the body. RDEA594 normalizes the amount of uric acid
excreted by gout patients. Since the majority of gout patients
are under-excreters, normalizing uric acid excretion
by moderating URAT1 transporter activity with RDEA594 may
provide the most physiologically appropriate and effective means
of reducing blood or sUA levels. In addition, because RDEA594
works by increasing the excretion of uric acid rather than
reducing the bodys production of uric acid, it can be used
in combination with sUA lowering agents that reduce the
production of uric acid such as allopurinol or febuxostat
(Uloric®,
Takeda Pharmaceutical Company Limited).
Allopurinol is the most commonly prescribed sUA lowering drug in
the United States, currently accounting for greater than
90 percent of U.S. unit sales of sUA lowering drugs.
However, in recent controlled clinical studies, only
30-40 percent
of gout patients achieved an adequate response to allopurinol as
defined by the achievement of sUA levels of less than
6 mg/dL, a commonly used medical target. We are developing
RDEA594, both as monotherapy and to be used in combination with
drugs like allopurinol, in order to treat patients not
adequately responding to their current therapy.
S-1
To date, results from our RDEA594 Phase 2 development program
have indicated RDEA594s clinical utility, as follows:
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In a Phase 2b study (Study 203) in 208 allopurinol
refractory gout patients, adding RDEA594 to allopurinol produced
highly statistically significant reductions in sUA of up to
30 percent with up to 89 percent of patients taking
the combination reaching the medically recommended target of
reducing sUA to below 6 mg/dL at the highest dose tested.
The combination of RDEA594 and allopurinol was also well
tolerated, with no serious adverse events and only two
discontinuations due to adverse events on RDEA594. Patients
admitted to the study had sUA levels greater than or equal to
6 mg/dL despite being on a stable dose of allopurinol. In
this 28-day,
randomized, double-blind, placebo-controlled study, each patient
received once daily doses of 200 mg of RDEA594, 400 mg
of RDEA594, 600 mg of RDEA594 or placebo while remaining on
the stable dose of allopurinol such patient was receiving when
he or she entered the study. Mean reductions in sUA after
4 weeks on 200 mg, 400 mg and 600 mg of
RDEA594 plus a standard dose of allopurinol were
16 percent, 22 percent and 30 percent,
respectively, compared to an increase in sUA of 3 percent
on placebo. Response rates on this study increased in a
dose-related manner and were highly clinically and statistically
significant at all dose levels when compared to allopurinol
alone. Using a last observation carried forward
(LOCF) analysis, which was the method utilized for the
U.S. approval of
Uloric®,
the response rates for the 200 mg, 400 mg and
600 mg plus a standard dose of allopurinol were
71 percent, 76 percent and 89 percent,
respectively, compared to 29 percent on allopurinol alone.
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In a Phase 1b clinical pharmacology study evaluating the use of
RDEA594 in combination with febuxostat (Study 111) in 21
gout patients with hyperuricemia (sUA greater than or equal to
8 mg/dL), 100 percent of patients receiving the
combination of RDEA594 and febuxostat achieved sUA levels below
the clinically important target level of 6 mg/dL, compared
to 67 percent and 56 percent for patients receiving
40 mg and 80 mg, respectively, of febuxostat alone. At
the highest combination doses tested (600 mg RDEA594
combined with 80 mg febuxostat), 100 percent of
patients reached sUA levels below 4 mg/dL, with
58 percent achieving levels below 3 mg/dL. No patient
achieved these reduced sUA levels on either dose of febuxostat
alone. The combination of RDEA594 and febuxostat was also well
tolerated, with no serious adverse events or discontinuations
due to adverse events and no clinically relevant drug
interactions observed between RDEA594 and febuxostat.
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In a 20-patient Phase 1b clinical pharmacology study evaluating
the use of RDEA594 in combination with 300 mg of
allopurinol (Study 110) in gout patients with hyperuricemia
(sUA greater than or equal to 8mg/dL), 100 percent of
patients at all combination doses evaluated achieved sUA levels
below the target of 6 mg/dL, compared to 20 percent of
patients on allopurinol alone. Of patients receiving RDEA594
600 mg alone, 67 percent achieved sUA levels below
6 mg/dL, which was significantly higher than the percent
reaching target on allopurinol alone (p < 0.05). At the
highest combination doses tested (600 mg of RDEA594
combined with 300 mg of allopurinol), 90 percent of
patients reached sUA levels below 5 mg/dL, and
50 percent reached levels below 4 mg/dL. The
combination of RDEA594 and allopurinol was well tolerated, with
no serious adverse events or discontinuations that were
considered possibly related to RDEA594 or the combination. No
clinically relevant drug interactions were observed between
RDEA594 and allopurinol in this study; however, plasma levels of
oxypurinol, an active metabolite of allopurinol, were decreased
approximately 25-35 percent.
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When administered as a single agent in a Phase 2b study (Study
202), RDEA594 was well tolerated and produced significant
reductions in uric acid in the blood. In this randomized,
double-blind, placebo-controlled, dose-escalation study of 123
gout patients with hyperuricemia (sUA levels greater than or
equal to 8 mg/dL) the primary endpoint was a significant
increase in the proportion of patients who achieved a response,
defined as a reduction of uric acid in the
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S-2
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blood to < 6 mg/dL after four weeks of treatment,
compared to placebo. The primary endpoint was achieved, uric
acid decreased and response rates increased in a dose-related
manner and were highly clinically and statistically significant
at the two highest doses tested. At the highest dose the
response rate was 60 percent, compared to 0 percent
for placebo (p < 0.0001). RDEA594 was also well tolerated
in this study, with no serious adverse events and only two
discontinuations due to adverse events on RDEA594.
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Results from multiple studies have indicated that the activity
of RDEA594 is not diminished in patients with mild renal
impairment. A smaller dataset from Study 202 indicate that after
4 weeks of monotherapy with RDEA594, patients with moderate
renal impairment had similar reductions in sUA as compared to
patients with no renal impairment.
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We are also developing next-generation inhibitors of the URAT1
transporter for the treatment of gout patients with
hyperuricemia. Based on preclinical results, our next-generation
inhibitors demonstrate many of the same positive attributes as
RDEA594, but with greater potency against the URAT1 transporter.
Preclinical development activities with respect to these
next-generation product candidates are ongoing.
Cancer
Mitogen-activated ERK kinase (MEK) is believed to
play an important role in cancer cell proliferation, apoptosis
and metastasis. BAY
86-9766
(formerly known as RDEA119) is a potent and selective inhibitor
of MEK in development for the treatment of cancer. In vivo
preclinical tests have shown BAY
86-9766 to
have potent anti-tumor activity. In addition, preclinical
in vitro and in vivo studies of BAY
86-9766 have
demonstrated synergistic activity across multiple tumor types
when BAY
86-9766 is
used in combination with other anti-cancer agents, including
sorafenib
(Nexavar®,
Bayer HealthCare AG (Bayer) and Onyx
Pharmaceuticals, Inc.).
In April 2009, we entered into a global license agreement with
Bayer to develop and commercialize MEK inhibitors for the
treatment of cancer. Under the license agreement, we are
responsible for the completion of the Phase 1 and Phase 1/2
studies. Thereafter, Bayer will be responsible for the further
development and commercialization of BAY
86-9766 and
any of our other MEK inhibitors.
We have completed our Phase 1 study of BAY
86-9766 as a
single agent in advanced cancer patients with different tumor
types and we have identified the maximum tolerated dose
(MTD) of BAY
86-9766 in
our Phase 1/2 study in combination with sorafenib. Dosing in the
MTD expansion cohort of the Phase 1/2 study is ongoing.
Phase 1 results to date in refractory patients with advanced
solid tumors have demonstrated that BAY
86-9766 is
well tolerated with a number of patients achieving stable
disease or partial response to treatment. Based on the
preclinical and Phase 1/2 results, Bayer recently initiated a
Phase 2 study of BAY
86-9766 in
combination with sorafenib as first-line therapy for primary
liver cancer.
Market
Opportunity
We believe that there is a significant market opportunity for
our products, should they be successfully developed, approved
and commercialized.
We believe that there is a significant need for new products for
the treatment and prevention of gout. There have been only two
new products approved in the United States for the treatment of
gout in the last 40 years. According to the Decision
Resources, an estimated 19.7 million adults in the seven
major markets (the United States, Japan, France, Germany, Italy,
Spain and United Kingdom) suffer from gout. The incidence and
severity of gout is increasing in the United States. According
to the Annals of Rheumatic Diseases, there
S-3
was a 288% increase in gout-related hospitalizations from
1988-2005
and over $11.2 billion in gout-related hospital costs were
incurred in 2005 in the United States. Many chronic gout
sufferers are unable to achieve target reductions in uric acid
with current treatments. Scientists have recently discovered
defects in multiple transporters in the kidney that play
important roles in uric acid transport and are genetically
linked to a higher risk of gout. URAT1 has been identified as
the most important transporter for uric acid. We are developing
products for the treatment of hyperuricemia and gout that
inhibit URAT1, thereby increasing the excretion of uric acid and
lowering serum uric acid levels. In addition, we believe there
may be opportunities to develop uric acid-lowering agents to
treat diseases other than gout. Evidence suggests that the
chronic elevation of uric acid associated with gout, known as
hyperuricemia, may also have systemic consequences, including an
increased risk for kidney dysfunction, elevated C-reactive
protein, hypertension and possibly other cardiovascular risk
factors.
We also believe that there is growing interest in the potential
for targeted therapies, including kinase inhibitors, for the
treatment of both cancer and inflammatory disease. Sales of
products used in the treatment of cancer were $52.4 billion
in 2009 according to IMS Health Incorporated, fueled by strong
acceptance of innovative and effective targeted therapies. In
addition to cancer, MEK appears to play a role in inflammatory
diseases and we believe that BAY
86-9766 and
our next generation MEK inhibitors, if successfully developed,
approved and commercialized, could participate in these growing
markets.
Bayer
Relationship
Under the terms of our license agreement with Bayer, we granted
to Bayer a worldwide, exclusive license to develop and
commercialize our MEK inhibitors for all indications. In June
2009, Bayer paid us a non-refundable, upfront cash payment of
$35 million in partial consideration for the exclusive
right to develop and commercialize our MEK inhibitors. In
January 2011, we received a $15 million milestone payment
from Bayer triggered by the initiation of a Phase 2 study
evaluating BAY
86-9766 in
combination with sorafenib for the treatment of hepatocellular
carcinoma or primary liver cancer. Potential payments under the
license agreement with Bayer could total up to
$407 million, not including royalties. This amount includes
the upfront cash payment and the $15 million milestone
payment we received in January 2011, as well as additional cash
payments upon achievement of certain development, regulatory and
sales-based milestones. We are also eligible to receive low
double-digit royalties on sales of products under the license
agreement.
Valeant
Relationship
In December 2006, we acquired intellectual property and other
assets from Valeant Research & Development, Inc.
(Valeant) related to RDEA806 and our next generation
non-nucleoside reverse transcriptase inhibitor
(NNRTI) program, as well as BAY
86-9766 and
our next generation MEK inhibitor program. In consideration for
the assets purchased from Valeant and subject to the
satisfaction of certain conditions, Valeant received certain
rights, including the right to receive from us development-based
milestone payments and sales-based royalty payments. There is
one set of potential milestones totaling up to $25 million
for RDEA806 and the next generation NNRTI program, and a
separate set of potential milestones totaling up to
$17 million for BAY
86-9766 and
the next generation MEK inhibitor program. The first milestone
payment of $2 million in the NNRTI program would be due
after the first patient is dosed in the first Phase 2b study.
The first milestone payment of $1 million in the MEK
inhibitor program was paid to Valeant in January 2011 in
connection with the initiation of a Phase 2 study relating
to BAY 86-9766. The royalty rates on all products under our
agreement with Valeant are in the mid-single digits.
S-4
Financial
Update
We estimate that the total amount of our cash, cash equivalents
and short-term investments,
available-for-sale
as of December 31, 2010 was approximately
$80.6 million. This amount is preliminary, has not been
audited and is subject to change upon completion of our ongoing
audit. Moreover, this amount does not reflect the
$15 million milestone payment we received in January 2011
described above. Additional information and disclosures would be
required for a more complete understanding of our financial
position and results of operations as of December 31, 2010.
Corporate
Information
We were incorporated in the State of Delaware in January 1994.
Our principal executive offices are located at
4939 Directors Place, San Diego, CA 92121. Our
telephone number is
(858) 652-6500.
Our website address is www.ardeabio.com. The information
contained in, or that can be accessed through, our website is
not part of, and is not incorporated into, this prospectus
supplement or the accompanying prospectus and should not be
considered part of this prospectus supplement or the
accompanying prospectus.
S-5
THE
OFFERING
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Common stock offered by us |
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2,750,000 shares |
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Common stock to be outstanding immediately after this offering
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26,116,979 shares |
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Overallotment option |
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The underwriters have an option to purchase up to 412,500
additional shares of our common stock to cover overallotments,
if any. The underwriters may exercise this option at any time
within 30 days from the date of this prospectus supplement. |
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Use of proceeds |
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We intend to use the net proceeds from this offering for general
corporate purposes, including clinical trial expenses, research
and development expenses and general and administrative
expenses, including working capital. See the sections entitled
Use of Proceeds and Underwriting in this
prospectus supplement. |
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Nasdaq Global Select Market symbol |
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RDEA |
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Risk factors |
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An investment in our common stock involves a high degree of
risk. See the section entitled Risk Factors in this
prospectus supplement. |
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Insider participation |
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As part of this offering, the underwriters are selling an
aggregate of 577,400 shares of our common stock to entities
affiliated with two of our directors and principal stockholders,
Felix J. Baker and Kevin C. Tang, at the public offering price
set forth on the cover page of this prospectus. |
The number of shares of our common stock to be outstanding
immediately after this offering is based on
23,366,979 shares outstanding as of December 31, 2010
and excludes:
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3,538,191 shares of our common stock issuable upon the
exercise of options outstanding as of December 31, 2010,
having a weighted-average exercise price of approximately $14.46
per share;
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684,332 shares of our common stock subject to warrants
outstanding as of December 31, 2010, having an exercise
price of $11.14 per share; and
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an aggregate of 1,247,390 shares of common stock reserved
for future issuance under our 2002 Non-Officer Equity Incentive
Plan, as amended, 2000 Employee Stock Purchase Plan, and Amended
and Restated 2004 Stock Incentive Plan as of December 31,
2010.
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Except as otherwise indicated, all information in the prospectus
supplement assumes no exercise by the underwriters of their
overallotment option.
S-6
RISK
FACTORS
An investment in our common stock involves a high degree of
risk. Before deciding whether to invest in our common stock, you
should consider carefully the risks described below and
discussed under the section captioned Risk Factors
contained in our Quarterly Report on
Form 10-Q
for the quarterly period ended September 30, 2010, which
are incorporated by reference in this prospectus supplement and
the accompanying prospectus in their entirety, together with the
other information in this prospectus supplement, the
accompanying prospectus, the information and documents
incorporated by reference, and in any free writing prospectus
prepared by or on behalf of us that we have authorized for use
in connection with this offering. If any of these risks actually
occur, our business, financial condition, results of operations
or cash flows could be seriously harmed. This could cause the
trading price of our common stock to decline, resulting in a
loss of all or part of your investment.
Risks
Related to this Offering
Management
will have broad discretion as to the use of the proceeds from
this offering, and we may not use the proceeds
effectively.
Our management will have broad discretion in the application of
the net proceeds from this offering and could spend the proceeds
in ways that do not improve our results of operations or enhance
the value of our common stock. Our failure to apply these funds
effectively could have a material adverse effect on our
business, delay the development of our product candidates and
cause the price of our common stock to decline.
You
will experience immediate and substantial dilution in the net
tangible book value per share of the common stock you
purchase.
Since the price per share of our common stock being offered is
substantially higher than the net tangible book value per share
of our common stock, you will suffer substantial dilution in the
net tangible book value of the common stock you purchase in this
offering. Based on the public offering price of $26.00 per
share, and our net tangible book value per share as of
September 30, 2010, if you purchase shares of common stock
in this offering, you will suffer immediate and substantial
dilution of $20.54 per share in the net tangible book value of
the common stock. See the section entitled Dilution
below for a more detailed discussion of the dilution you would
incur if you purchase common stock in this offering.
You
may experience future dilution as a result of future equity
offerings or other equity issuances.
In order to raise additional capital, we may in the future offer
additional shares of our common stock or other securities
convertible into or exchangeable for our common stock. We cannot
assure you that we will be able to sell shares or other
securities in any other offering at a price per share that is
equal to or greater than the price per share paid by investors
in this offering, and investors purchasing shares or other
securities in the future could have rights superior to existing
stockholders. The price per share at which we sell additional
shares of our common stock or other securities convertible into
or exchangeable for our common stock in future transactions may
be higher or lower than the price per share in this offering. As
of December 31, 2010, an aggregate of 1,247,390 shares
of common stock were reserved and available for future grant
under our 2002 Non-Officer Equity Incentive Plan, as amended,
2000 Employee Stock Purchase Plan, and Amended and Restated 2004
Stock Incentive Plan. Also as of such date, options to purchase
3,538,191 shares of our common stock and warrants to
purchase 684,332 shares of our common stock were
outstanding. You will incur dilution upon the grant of any
shares pursuant to any of such plans, upon vesting of any stock
awards under any of such plans, or upon exercise of any such
outstanding options or warrants.
S-7
FORWARD-LOOKING
STATEMENTS
This prospectus supplement, the accompanying prospectus, the
documents we have filed with the SEC that are incorporated
herein by reference and any free writing prospectus prepared by
or on behalf of us or to which we have referred you contain
forward-looking statements within the meaning of
Section 27A of the Securities Act of 1933, or Securities
Act, as amended, and Section 21E of the Securities Exchange
Act of 1934, as amended, or Exchange Act. These statements are
based on our current expectations, assumptions, estimates and
projections about our business and our industry, and involve
known and unknown risks, uncertainties and other factors that
may cause our results, levels of activity, performance or
achievement to be materially different from any future results,
levels of activity, performance or achievements expressed or
implied by the forward-looking statements. Forward-looking
statements include, but are not limited to, statements about:
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the safety and efficacy of our product candidates;
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the progress, timing and results of clinical trials and research
and development efforts involving our product candidates;
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the submission and timing of applications for regulatory
approvals;
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our ability to obtain and maintain regulatory approvals for our
product candidates;
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our expectations with regard to our intellectual property
position and our ability to successfully protect our
intellectual property;
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our plans to conduct future clinical trials or research and
development efforts;
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estimates of the potential markets for our product candidates;
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our operating and growth strategies, industry, planned products,
and our expected future revenues, operations and expenditures
and projected cash needs;
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our expectations about partnering, acquisitions, licensing and
marketing;
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our estimated cash and cash equivalents and short-term
investments;
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the use of proceeds from this offering; and
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economic conditions, both generally and those specifically
related to the biotechnology industry.
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In some cases, you can identify forward-looking statements by
terms such as anticipate, believe,
could, estimate, expect,
intend, may, plan,
potential, predict, project,
should, will, would and
similar expressions intended to identify forward-looking
statements. While we believe that we have a reasonable basis for
each forward-looking statement, we caution you that these
statements are based on a combination of facts and factors
currently known by us and our projections of the future, about
which we cannot be certain. We discuss many of these risks,
uncertainties and other factors in greater detail under the
sections captioned Risk Factors contained in this
prospectus supplement and in our Quarterly Report on
Form 10-Q
for the quarterly period ended September 30, 2010. Given
these risks, uncertainties and other factors, you should not
place undue reliance on these forward-looking statements. Also,
these forward-looking statements represent our estimates and
assumptions only as of the date such forward-looking statements
are made. You should read carefully both this prospectus
supplement and the accompanying prospectus, together with the
information incorporated herein by reference as described under
the heading Information Incorporated by Reference in
this prospectus supplement, completely and with the
understanding that our actual future results may be materially
different from what we expect. We hereby qualify all of our
forward-looking statements by these cautionary statements.
Except as required by law, we assume no obligation to update
these forward-looking statements publicly, or to update the
reasons actual results could differ materially from those
anticipated in these forward-looking statements, even if new
information becomes available in the future.
S-8
USE OF
PROCEEDS
We estimate that the net proceeds from the sale of the
2,750,000 shares of common stock that we are offering will
be approximately $67.8 million, or approximately
$77.9 million if the underwriters exercise in full their
option to purchase 412,500 additional shares of common stock,
based on the public offering price of $26.00 per share and after
deducting the underwriting discount and estimated offering
expenses payable by us. For more details, see the section
entitled Underwriting in this prospectus supplement.
We intend to use the net proceeds from this offering for general
corporate purposes, including clinical trial expenses, research
and development expenses and general and administrative
expenses, including working capital. We may also use a portion
of the net proceeds from this offering to in-license, invest in
or acquire businesses, technologies, product candidates or other
intellectual property that we believe are complementary to our
own, although we have no current plans, commitments or
agreements to do so as of the date of this prospectus
supplement. The amounts and timing of these expenditures will
depend on a number of factors, such as the timing, scope,
progress and results of our research and development efforts,
the timing and progress of any partnering efforts, and the
competitive environment for our product candidates. As of the
date of this prospectus supplement, we cannot specify with
certainty all of the particular uses of the net proceeds to us
from this offering. Accordingly, we will retain broad discretion
over the use of these proceeds. Pending application of the net
proceeds as described above, we intend to temporarily invest the
net proceeds in interest-bearing, investment-grade securities.
S-9
DILUTION
Our net tangible book value as of September 30, 2010 was
approximately $73.0 million, or $3.17 per share. Net
tangible book value per share is determined by dividing our
total tangible assets, less total liabilities, by the number of
shares of our common stock outstanding as of September 30,
2010. Dilution in net tangible book value per share represents
the difference between the amount per share paid by purchasers
of shares of common stock in this offering and the net tangible
book value per share of our common stock immediately after this
offering.
After giving effect to the sale of 2,750,000 shares of our
common stock in this offering at the public offering price of
$26.00 per share and after deducting the underwriting discount
and estimated offering expenses payable by us, our as adjusted
net tangible book value as of September 30, 2010 would have
been approximately $140.9 million, or $5.46 per share. This
represents an immediate increase in net tangible book value of
$2.29 per share to existing stockholders and immediate dilution
in net tangible book value of $20.54 per share to new investors
purchasing our common stock in this offering at the assumed
public offering price. The following table illustrates this
dilution on a per share basis:
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Public offering price per share
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$
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26.00
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Net tangible book value per share as of September 30, 2010
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$
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3.17
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Increase per share attributable to investors purchasing our
common stock in this offering
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2.29
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As adjusted net tangible book value per share after this offering
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5.46
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Dilution per share to investors purchasing our common stock in
this offering
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$
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20.54
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If the underwriters exercise in full their option to purchase
412,500 additional shares of common stock at the public offering
price of $26.00 per share, the as adjusted net tangible book
value after this offering would be $5.75 per share, representing
an increase in net tangible book value of $2.58 per share to
existing stockholders and immediate dilution in net tangible
book value of $20.25 per share to new investors purchasing our
common stock in this offering at the assumed public offering
price.
The number of shares of our common stock to be outstanding
immediately after this offering is based on
23,076,321 shares outstanding as of September 30, 2010
and excludes:
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3,200,217 shares of our common stock issuable upon the
exercise of options outstanding as of September 30, 2010,
having a weighted-average exercise price of approximately $12.23
per share;
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684,332 shares of our common stock subject to warrants
outstanding as of September 30, 2010, having an exercise
price of $11.14 per share; and
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an aggregate of 1,876,022 shares of common stock reserved
for future issuance under our 2002 Non- Officer Equity Incentive
Plan, as amended, 2000 Employee Stock Purchase Plan, and Amended
and Restated 2004 Stock Incentive Plan as of September 30,
2010.
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To the extent that outstanding options or warrants are
exercised, you will experience further dilution. In addition, we
may choose to raise additional capital due to market conditions
or strategic considerations even if we believe we have
sufficient funds for our current or future operating plans. To
the extent that additional capital is raised through the sale of
equity or convertible debt securities, the issuance of these
securities could result in further dilution to our stockholders.
S-10
UNDERWRITING
Merrill Lynch, Pierce, Fenner & Smith Incorporated and
Jefferies & Company, Inc. are acting as
representatives of each of the underwriters named below. Subject
to the terms and conditions set forth in an underwriting
agreement among us and the underwriters, we have agreed to sell
to the underwriters, and each of the underwriters has agreed,
severally and not jointly, to purchase from us, the number of
shares of common stock set forth opposite its name below.
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Number of
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Underwriter
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Shares
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Merrill Lynch, Pierce, Fenner & Smith
Incorporated
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1,567,500
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Jefferies & Company, Inc.
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495,000
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JMP Securities LLC
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275,000
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Brean Murray, Carret & Co., LLC
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275,000
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Roth Capital Partners, LLC
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137,500
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Total
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2,750,000
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Subject to the terms and conditions set forth in the
underwriting agreement, the underwriters have agreed, severally
and not jointly, to purchase all of the shares sold under the
underwriting agreement if any of these shares are purchased. If
an underwriter defaults, the underwriting agreement provides
that the purchase commitments of the nondefaulting underwriters
may be increased or the underwriting agreement may be terminated.
We have agreed to indemnify the underwriters against certain
liabilities, including liabilities under the Securities Act, or
to contribute to payments the underwriters may be required to
make in respect of those liabilities.
The underwriters are offering the shares, subject to prior sale,
when, as and if issued to and accepted by them, subject to
approval of legal matters by their counsel, including the
validity of the shares, and other conditions contained in the
underwriting agreement, such as the receipt by the underwriters
of officers certificates and legal opinions. The
underwriters reserve the right to withdraw, cancel or modify
offers to the public and to reject orders in whole or in part.
Commissions
and Discounts
The representatives have advised us that the underwriters
propose initially to offer the shares to the public at the
public offering price set forth on the cover page of this
prospectus and to dealers at that price less a concession not in
excess of $0.93 per share. After the initial offering, the
public offering price, concession or any other term of the
offering may be changed.
The underwriters have agreed to sell an aggregate of
577,400 shares of our common stock to entities affiliated
with two of our directors and principal stockholders,
Felix J. Baker and Kevin C. Tang, at the public
offering price set forth on the cover page of this prospectus
supplement. The underwriters will not receive any underwriting
discount on the sale of such shares.
The following table shows the per share and total underwriting
discount (other than in connection with the sale of
577,400 shares of our common stock to entities affiliated
with two of our directors and
S-11
principal stockholders). The information assumes either no
exercise or full exercise by the underwriters of their
overallotment option.
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Without Option
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With Option
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Per share
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$1.56
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$1.56
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Total
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$3,389,256
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$4,032,756
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The expenses of the offering, not including the underwriting
discount, are estimated at $300,000 and are payable by us.
However, the underwriters have agreed to reimburse us for
certain of our expenses incurred in connection with this
offering.
Overallotment
Option
We have granted an option to the underwriters, exercisable for
30 days after the date of this prospectus, to purchase up
to 412,500 additional shares at the public offering price,
less the underwriting discount. The underwriters may exercise
this option solely to cover any overallotments. If the
underwriters exercise this option, each will be obligated,
subject to conditions contained in the underwriting agreement,
to purchase a number of additional shares proportionate to that
underwriters initial amount reflected in the above table.
No Sales
of Similar Securities
We, our executive officers and directors and certain of our
principal stockholders have agreed not to sell or transfer any
common stock or securities convertible into, exchangeable for,
exercisable for common stock, for 90 days after the date of
this prospectus without first obtaining the written consent of
Merrill Lynch, Pierce, Fenner & Smith Incorporated.
Specifically, we and these other persons have agreed, with
certain limited exceptions, not to directly or indirectly:
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offer, pledge, transfer, sell or contract or grant any option to
sell (including without limitation any short sale) any shares of
common stock;
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establish an open put equivalent position within the
meaning of
Rule 16a-1(h)
under the Exchange Act of shares of common stock; or
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otherwise dispose of any shares of common stock, options or
warrants to acquire shares of common stock.
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This lock-up
provision applies to common stock and to securities convertible
into or exchangeable or exercisable for or repayable with common
stock. It also applies to common stock owned now or acquired
later by the person executing the agreement or for which the
person executing the agreement later acquires the power of
disposition. In the event that either (x) during the last
17 days of the
lock-up
period referred to above, we issue an earnings release or
material news or a material event relating to the Company occurs
or (y) prior to the expiration of the
lock-up
period, we announce that we will release earnings results or
become aware that material news or a material event will occur
during the
16-day
period beginning on the last day of the
lock-up
period, the restrictions described above shall continue to apply
until the expiration of the
18-day
period beginning on the issuance of the earnings release or the
occurrence of the material news or material event.
S-12
Nasdaq
Global Select Market Listing
The shares are listed on the Nasdaq Global Select Market under
the symbol RDEA.
Price
Stabilization, Short Positions
Until the distribution of the shares is completed, SEC rules may
limit underwriters and selling group members from bidding for
and purchasing our common stock. However, the representatives
may engage in transactions that stabilize the price of the
common stock, such as bids or purchases to peg, fix or maintain
that price.
In connection with the offering, the underwriters may purchase
and sell our common stock in the open market. These transactions
may include short sales, purchases on the open market to cover
positions created by short sales and stabilizing transactions.
Short sales involve the sale by the underwriters of a greater
number of shares than they are required to purchase in the
offering. Covered short sales are sales made in an
amount not greater than the underwriters overallotment
option described above. The underwriters may close out any
covered short position by either exercising their overallotment
option or purchasing shares in the open market. In determining
the source of shares to close out the covered short position,
the underwriters will consider, among other things, the price of
shares available for purchase in the open market as compared to
the price at which they may purchase shares through the
overallotment option. Naked short sales are sales in
excess of the overallotment option. The underwriters must close
out any naked short position by purchasing shares in the open
market. A naked short position is more likely to be created if
the underwriters are concerned that there may be downward
pressure on the price of our common stock in the open market
after pricing that could adversely affect investors who purchase
in the offering. Stabilizing transactions consist of various
bids for or purchases of shares of common stock made by the
underwriters in the open market prior to the completion of the
offering.
Similar to other purchase transactions, the underwriters
purchases to cover the syndicate short sales may have the effect
of raising or maintaining the market price of our common stock
or preventing or retarding a decline in the market price of our
common stock. As a result, the price of our common stock may be
higher than the price that might otherwise exist in the open
market. The underwriters may conduct these transactions on the
Nasdaq Global Select Market, in the
over-the-counter
market or otherwise.
Neither we nor any of the underwriters make any representation
or prediction as to the direction or magnitude of any effect
that the transactions described above may have on the price of
our common stock. In addition, neither we nor any of the
underwriters make any representation that the representatives
will engage in these transactions or that these transactions,
once commenced, will not be discontinued without notice.
Passive
Market Making
In connection with this offering, underwriters and selling group
members may engage in passive market making transactions in the
common stock on the Nasdaq Global Select Market in accordance
with Rule 103 of Regulation M under the Exchange Act
during a period before the commencement of offers or sales of
common stock and extending through the completion of
distribution. A passive market maker must display its bid at a
price not in excess of the highest independent bid of that
security. However, if all independent bids are lowered below the
passive market makers bid, that bid must then be lowered
when specified purchase limits are exceeded. Passive market
making may cause the price of our common stock to be higher than
the price that otherwise would exist in the open market in the
absence of those transactions. The underwriters and dealers are
not required to engage in passive market making and may end
passive market making activities at any time.
S-13
Electronic
Offer, Sale and Distribution of Shares
In connection with the offering, certain of the underwriters or
securities dealers may distribute prospectuses by electronic
means, such as
e-mail. In
addition, certain of the underwriters may facilitate Internet
distribution for this offering to certain of their Internet
subscription customers. Certain of the underwriters may allocate
a limited number of shares for sale to their online brokerage
customers. An electronic prospectus is available on the Internet
web sites maintained by certain of the underwriters. Other than
the prospectus in electronic format, the information under such
underwriters web sites is not part of this prospectus.
Other
Relationships
Some of the underwriters and their affiliates have engaged in,
and may in the future engage in, investment banking and other
commercial dealings in the ordinary course of business with us
or our affiliates. They have received, or may in the future
receive, customary fees and commissions for these transactions.
In addition, in the ordinary course of their business
activities, the underwriters and their affiliates may make or
hold a broad array of investments and actively trade debt and
equity securities (or related derivative securities) and
financial instruments (including bank loans) for their own
account and for the accounts of their customers. Such
investments and securities activities may involve securities
and/or
instruments of ours or our affiliates. The underwriters and
their affiliates may also make investment recommendations
and/or
publish or express independent research views in respect of such
securities or financial instruments and may hold, or recommend
to clients that they acquire, long
and/or short
positions in such securities and instruments.
Notice to
Prospective Investors in the EEA
In relation to each Member State of the European Economic Area
which has implemented the Prospectus Directive (each, a
Relevant Member State) an offer to the public of any
securities which are the subject of the offering contemplated by
this prospectus supplement (the Shares) may not be
made in that Relevant Member State except that an offer to the
public in that Relevant Member State of any Shares may be made
at any time under the following exemptions under the Prospectus
Directive, if they have been implemented in that Relevant Member
State:
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(a)
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to legal entities which are authorised or regulated to operate
in the financial markets or, if not so authorised or regulated,
whose corporate purpose is solely to invest in securities;
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(b)
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to any legal entity which has two or more of (1) an average
of at least 250 employees during the last financial year;
(2) a total balance sheet of more than 43,000,000 and
(3) an annual net turnover of more than 50,000,000,
as shown in its last annual or consolidated accounts;
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(c)
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by the Managers to fewer than 100 natural or legal persons
(other than qualified investors as defined in the Prospectus
Directive) subject to obtaining the prior consent of the
underwriters for any such offer; or
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(d)
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in any other circumstances falling within Article 3(2) of
the Prospectus Directive,
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provided that no such offer of Shares shall result in a
requirement for the publication by us or any Manager of a
prospectus pursuant to Article 3 of the Prospectus
Directive.
Any person making or intending to make any offer of securities
within the EEA should only do so in circumstances in which no
obligation arises for us or any of the underwriters to produce a
prospectus for such
S-14
offer. Neither we nor the underwriters have authorized, nor do
they authorize, the making of any offer of securities through
any financial intermediary, other than offers made by the
underwriters which constitute the final offering of securities
contemplated in this prospectus.
For the purposes of this provision, the expression an
offer to the public in relation to any Shares in any
Relevant Member State means the communication in any form and by
any means of sufficient information on the terms of the offer
and any Shares to be offered so as to enable an investor to
decide to purchase any Shares, as the same may be varied in that
Member State by any measure implementing the Prospectus
Directive in that Member State and the expression
Prospectus Directive means Directive 2003/71/EC and
includes any relevant implementing measure in each Relevant
Member State.
Each person in a Relevant Member State who receives any
communication in respect of, or who acquires any securities
under, the offer of securities contemplated by this prospectus
will be deemed to have represented, warranted and agreed to and
with us and each underwriter that:
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(A)
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it is a qualified investor within the meaning of the
law in that Relevant Member State implementing
Article 2(1)(e) of the Prospectus Directive; and
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(B)
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in the case of any securities acquired by it as a financial
intermediary, as that term is used in Article 3(2) of the
Prospectus Directive, (i) the securities acquired by it in
the offering have not been acquired on behalf of, nor have they
been acquired with a view to their offer or resale to, persons
in any Relevant Member State other than qualified
investors (as defined in the Prospectus Directive), or in
circumstances in which the prior consent of the representatives
has been given to the offer or resale; or (ii) where
securities have been acquired by it on behalf of persons in any
Relevant Member State other than qualified investors, the offer
of those securities to it is not treated under the Prospectus
Directive as having been made to such persons.
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In addition, in the United Kingdom, this document is being
distributed only to, and is directed only at, and any offer
subsequently made may only be directed at persons who are
qualified investors (as defined in the Prospectus
Directive) (i) who have professional experience in matters
relating to investments falling within Article 19
(5) of the Financial Services and Markets Act 2000
(Financial Promotion) Order 2005, as amended (the
Order)
and/or
(ii) who are high net worth companies (or persons to whom
it may otherwise be lawfully communicated) falling within
Article 49(2)(a) to (d) of the Order (all such persons
together being referred to as relevant persons).
This document must not be acted on or relied on in the United
Kingdom by persons who are not relevant persons. In the United
Kingdom, any investment or investment activity to which this
document relates is only available to, and will be engaged in
with, relevant persons.
Notice to
Prospective Investors in Switzerland
The Shares may not be publicly offered in Switzerland and will
not be listed on the SIX Swiss Exchange (SIX) or on
any other stock exchange or regulated trading facility in
Switzerland. This document has been prepared without regard to
the disclosure standards for issuance prospectuses under art.
652a or art. 1156 of the Swiss Code of Obligations or the
disclosure standards for listing prospectuses under art. 27 ff.
of the SIX Listing Rules or the listing rules of any other stock
exchange or regulated trading facility in Switzerland. Neither
this document nor any other offering or marketing material
relating to the Shares or the offering may be publicly
distributed or otherwise made publicly available in Switzerland.
Neither this document nor any other offering or marketing
material relating to the offering, the Issuer, the Shares have
been or will be filed with or approved by any Swiss regulatory
authority. In particular, this document will not be filed with,
and the offer of Shares will not be supervised by, the Swiss
Financial Market Supervisory Authority FINMA (FINMA), and the
offer of Shares has not been and will not be authorized
S-15
under the Swiss Federal Act on Collective Investment Schemes
(CISA). The investor protection afforded to
acquirers of interests in collective investment schemes under
the CISA does not extend to acquirers of Shares.
Notice to
Prospective Investors in the Dubai International Financial
Centre
This offering memorandum relates to an Exempt Offer in
accordance with the Offered Securities Rules of the Dubai
Financial Services Authority (DFSA). This offering
memorandum is intended for distribution only to persons of a
type specified in the Offered Securities Rules of the DFSA. It
must not be delivered to, or relied on by, any other person. The
DFSA has no responsibility for reviewing or verifying any
documents in connection with Exempt Offers. The DFSA has not
approved this offering memorandum nor taken steps to verify the
information set forth herein and has no responsibility for the
offering memorandum. The securities to which this offering
memorandum relates may be illiquid
and/or
subject to restrictions on their resale. Prospective purchasers
of the securities offered should conduct their own due diligence
on the securities. If you do not understand the contents of this
offering memorandum you should consult an authorized financial
advisor.
S-16
LEGAL
MATTERS
The validity of the shares of common stock offered by this
prospectus supplement and the accompanying prospectus will be
passed upon for us by Cooley LLP, San Diego, California.
Latham & Watkins LLP, San Diego, California, is
counsel for the underwriters in connection with this offering.
EXPERTS
Stonefield Josephson, Inc., independent registered public
accounting firm, has audited our consolidated financial
statements as of and for the year ended December 31, 2009
and the effectiveness of our internal control over financial
reporting as of December 31, 2009, as set forth in their
reports, each of which are included in our Annual Report on
Form 10-K
for the year ended December 31, 2009 as filed with the SEC
on March 12, 2010, and are incorporated by reference in
this prospectus supplement and elsewhere in the registration
statement. These financial statements are incorporated by
reference in reliance on Stonefield Josephson, Inc.s
reports, given on their authority as experts in accounting and
auditing.
WHERE YOU
CAN FIND MORE INFORMATION
This prospectus supplement and the accompanying prospectus are
part of the registration statement on
Form S-3
we filed with the SEC under the Securities Act, and do not
contain all the information set forth in the registration
statement. Whenever a reference is made in this prospectus
supplement or the accompanying prospectus to any of our
contracts, agreements or other documents, the reference may not
be complete and you should refer to the exhibits that are a part
of the registration statement or the exhibits to the reports or
other documents incorporated by reference in this prospectus
supplement and the accompanying prospectus for a copy of such
contract, agreement or other document. Because we are subject to
the information and reporting requirements of the Securities
Exchange Act of 1934, as amended, we file annual, quarterly and
current reports, proxy statements and other information with the
SEC. Our SEC filings are available to the public over the
Internet at the SECs website at
http://www.sec.gov.
You may also read and copy any document we file at the
SECs Public Reference Room at 100 F Street,
N.E., Washington, D.C. 20549. Please call the SEC at
1-800-SEC-0330
for further information on the operation of the Public Reference
Room.
INFORMATION
INCORPORATED BY REFERENCE
We are allowed to incorporate by reference information contained
in documents that we file with the SEC. This means that we can
disclose important information to you by referring you to those
documents and that the information in this prospectus is not
complete. You should read the information incorporated by
reference for more detail. We incorporate by reference in two
ways. First, we list certain documents that we have already
filed with the SEC. The information in these documents is
considered part of this prospectus. Second, the information in
documents that we file in the future will update and supersede
the current information in, and incorporated by reference in,
this prospectus.
We incorporate by reference the documents listed below and any
filings we will make with the SEC under Section 13(a),
13(c), 14 or 15(d) of the Exchange Act of 1934, as amended,
after the date we filed the initial registration statement of
which this prospectus is a part and before the effective date of
the registration statement and any future filings we will make
with the SEC pursuant to Section 13(a), 13(c), 14 or 15(d)
of the Exchange Act of 1934, as amended, from the date of this
prospectus but prior to the termination of the offering (in each
case, except for the information in any of the foregoing Current
Reports on
Form 8-K
and
Form 8-K/A
furnished under Item 2.02 or Item 7.01 therein):
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our Annual Report on
Form 10-K
for the year ended December 31, 2009, filed with the SEC on
March 12, 2010 (including information specifically
incorporated by reference into our
Form 10-K
from our Proxy Statement for our 2010 Annual Meeting of
Stockholders);
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our Quarterly Report on
Form 10-Q
for the quarter ended March 31, 2010, filed with the SEC on
May 7, 2010;
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our Quarterly Report on
Form 10-Q
for the quarter ended June 30, 2010, filed with the SEC on
August 6, 2010;
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our Quarterly Report on
Form 10-Q
for the quarter ended September 30, 2010, filed with the
SEC on November 9, 2010;
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our Current Reports on
Form 8-K
filed with the SEC on February 9, 2010, March 8, 2010,
April 5, 2010, April 9, 2010, May 27, 2010,
September 17, 2010 , October 7, 2010 (as amended by
Amendment No. 1 to Current Report on
Form 8-K/A,
filed with the SEC on October 22, 2010), December 21,
2010 and January 19, 2010; and
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the description of our common stock set forth in our
registration statement on
Form 8-A12B
(File
No. 001-33734),
filed under the Exchange Act on October 9, 2007, and any
amendment or report filed for the purpose of updating that
description.
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You may request a copy of these filings at no cost, by writing
or telephoning us at the following address or telephone number:
Ardea Biosciences, Inc.
4939 Directors Place
San Diego, CA 92121
Attn: Investor Relations
(858) 652-6500
S-18
PROSPECTUS
$100,000,000
Ardea Biosciences, Inc.
Common Stock
Warrants
Units
Our common stock is listed on The NASDAQ Global Market under the
symbol RDEA. On November 15, 2010, the last
reported sale price of our common stock on The NASDAQ Global
Market was $22.29 per share.
We may, from time to time, offer to sell up to $100,000,000 of
any combination of the securities described in this prospectus,
either individually or in units, at prices and on terms
described in one or more supplements to this prospectus. We may
also offer common stock upon the exercise of warrants.
This prospectus describes some of the general terms that may
apply to an offering of our securities. The specific terms and
any other information relating to a specific offering will be
set forth in a post-effective amendment to the registration
statement of which this prospectus is a part or in a supplement
to this prospectus or may be set forth in one or more documents
incorporated by reference in this prospectus. You should read
this prospectus, the information incorporated by reference in
this prospectus and any prospectus supplement carefully before
you invest.
Investing in our securities involves a high degree of risk.
See Risk Factors on page 5 of this prospectus
and as updated in our future filings made with the Securities
and Exchange Commission, or the SEC, which are incorporated by
reference in this prospectus.
This prospectus may not be used to offer or sell any
securities unless accompanied by a prospectus supplement.
The securities may be sold by us to or through underwriters or
dealers, directly to purchasers or through agents designated
from time to time. For additional information on the methods of
sale, you should refer to the section entitled Plan of
Distribution in this prospectus. If any underwriters are
involved in the sale of any securities with respect to which
this prospectus is being delivered, the names of such
underwriters and any applicable discounts or commissions and
over-allotment options will be set forth in a prospectus
supplement. The price to the public of such securities and the
net proceeds we expect to receive from such sale will also be
set forth in a prospectus supplement.
Neither the SEC nor any state securities commission has
approved or disapproved of these securities or determined if
this prospectus is truthful or complete. Any representation to
the contrary is a criminal offense.
The date of this prospectus is
November 15, 2010.
TABLE OF
CONTENTS
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You should rely only on the information contained in or
incorporated by reference into this prospectus or any applicable
prospectus supplement. We have not authorized anyone to provide
you with different information. We are not making an offer to
sell or seeking an offer to buy securities under this prospectus
or any applicable prospectus supplement in any jurisdiction
where the offer or sale is not permitted. The information
contained in this prospectus, any applicable prospectus
supplement and the documents incorporated by reference herein
and therein are accurate only as of their respective dates,
regardless of the time of delivery of this prospectus or any
sale of a security.
ABOUT
THIS PROSPECTUS
This prospectus is part of a registration statement that we
filed with the SEC using a shelf registration
process. Under this shelf registration statement, we may sell
from time to time in one or more offerings up to a total dollar
amount of $100 million of common stock and warrants to
purchase common stock, either individually or in units, as
described in this prospectus. Each time we sell any type or
series of securities under this prospectus, we will provide a
prospectus supplement that will contain more specific
information about the terms of that offering. We may also add,
update or change in a prospectus supplement any of the
information contained in this prospectus or in documents we have
incorporated by reference into this prospectus. This prospectus,
together with any applicable prospectus supplement and the
documents incorporated by reference into this prospectus or such
prospectus supplement, include all material information relating
to this offering. You should carefully read both this prospectus
and any applicable prospectus supplement together with the
additional information described under Where You Can Find
More Information before buying securities in this offering.
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SUMMARY
To understand this offering fully and for a more complete
description of the legal terms of this offering as well as our
company and the securities being sold in this offering, you
should read carefully the entire prospectus, the prospectus
supplement and the other documents to which we may refer you,
including Risk Factors and our consolidated
financial statements and notes to those statements incorporated
by reference in this prospectus. Reference to we,
us, our, our company,
the Company, and RDEA refers to Ardea
Biosciences, Inc. and its subsidiary, unless the context
requires otherwise.
ARDEA
BIOSCIENCES, INC.
Overview
and Business Strategy
Ardea Biosciences, Inc., of San Diego, California, is a
biotechnology company focused on the development of
small-molecule therapeutics for the treatment of serious
diseases. The current status of our development programs is as
follows:
Product
Portfolio
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Product Candidate
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Target Indication
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Development Status
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RDEA594
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Gout
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Phase 2b ongoing
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Next-generation
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Gout
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Preclinical development ongoing
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BAY 86-9766
(formerly known as RDEA119)
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Cancer
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Phase 1 completed and Phase 1/2 ongoing
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Multiple candidates
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HIV
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Further development will be dependent upon our ability to
partner this program
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GOUT
Gout is a painful, debilitating and progressive disease caused
by abnormally elevated levels of uric acid in the blood stream.
While gout is a treatable condition, there are limited treatment
options, and a number of adverse effects are associated with
most current therapies.
Approximately 90 percent of gout patients are considered to
have a defect in their ability to excrete sufficient amounts of
uric acid and are classified as under-excreters of
uric acid, which leads to excessive levels of uric acid in the
blood. Our most advanced product candidate, RDEA594, is a
selective inhibitor of URAT1, a transporter in the kidney that
regulates uric acid excretion from the body. RDEA594 normalizes
the amount of uric acid excreted by gout patients. Since the
majority of gout patients are under-excreters,
normalizing uric acid excretion by moderating URAT1 transporter
activity with RDEA594 may provide the most physiologically
appropriate and effective means of reducing blood or serum uric
acid (sUA) levels when used alone or in combination
with other sUA lowering agents, such as allopurinol or
febuxostat
(Uloric®,
Takeda Pharmaceutical Company Limited;
Adenuric®,
Ipsen and Menarini), which act by reducing the production of
uric acid in the body.
To date, results from our Phase 2 development program have
indicated RDEA594s clinical utility, as follows:
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When administered as a single agent in a Phase 2b study (Study
202), RDEA594 was well tolerated and produced significant
reductions in uric acid in the blood. In this randomized,
double-blind, placebo-controlled, dose-escalation study of 123
gout patients with hyperuricemia (sUA levels greater than or
equal to 8 mg/dL) the primary endpoint was a significant
increase in the proportion of patients who achieved a response,
defined as a reduction of uric acid in the blood to <
6 mg/dL after four weeks of treatment, compared to placebo.
The primary endpoint was achieved, uric acid decreased and
response rates increased in a dose-related manner and were
highly clinically and statistically significant at the two
highest doses tested. At the highest dose the response rate was
60 percent, compared to 0 percent for placebo (p
< 0.0001). RDEA594 was also well tolerated in this study.
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The combination of RDEA594 and allopurinol in a Phase 2a study
(Study 201) in gout patients was well tolerated and reduced
sUA levels an additional 24 percent compared to allopurinol
alone. Interim results from an ongoing Phase 1b clinical
pharmacology study (Study 110) of RDEA594 in combination
with allopurinol demonstrated that the combination
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was well tolerated and produced 100 percent response rates
in gout patients receiving two different doses of RDEA594 in
combination with allopurinol.
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The combination of RDEA594 and febuxostat in a Phase 1 study
(Study 105) in healthy volunteers was well tolerated and
resulted in sUA reductions of approximately 70 to
80 percent from baseline.
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Results from multiple studies have indicated that the activity
of RDEA594 is not diminished in patients with mild to moderate
renal impairment.
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Additional results from our Phase 2 development program will
include data from a Phase 2b study (Study 203) evaluating
200 mg, 400 mg and 600 mg of RDEA594 as an add-on
to allopurinol in patients on a stable dose of allopurinol that
do not respond adequately to allopurinol alone, additional data
from a Phase 1b clinical pharmacology study (Study
110) evaluating the combination of RDEA594 and allopurinol
in gout patients and results from a Phase 1b dose-ranging study
(Study 111) of RDEA594 in combination with febuxostat in
gout patients.
Based on preclinical results, our next-generation inhibitors of
the URAT1 transporter for the treatment of gout patients with
hyperuricemia demonstrate many of the same positive attributes
as RDEA594, but with greater potency against the URAT1
transporter. Preclinical development activities with respect to
these next-generation product candidates are ongoing.
CANCER
Mitogen-activated ERK kinase (MEK) is believed to
play an important role in cancer cell proliferation, apoptosis
and metastasis. BAY
86-9766
(formerly known as RDEA119) is a potent and selective inhibitor
of MEK in development for the treatment of cancer. In vivo
preclinical tests have shown BAY
86-9766 to
have potent anti-tumor activity. In addition, preclinical
in vitro and in vivo studies of BAY
86-9766 have
demonstrated synergistic activity across multiple tumor types
when BAY
86-9766 is
used in combination with other anti-cancer agents, including
sorafenib
(Nexavar®,
Bayer HealthCare AG (Bayer) and Onyx
Pharmaceuticals, Inc.).
In April 2009, we entered into a global license agreement with
Bayer to develop and commercialize MEK inhibitors for the
treatment of cancer. Under the license agreement, we are
responsible for the completion of the ongoing Phase 1 and Phase
1/2 studies. Thereafter, Bayer will be responsible for the
further development and commercialization of BAY
86-9766 and
any of our other MEK inhibitors.
We have identified the maximum tolerated dose (MTD)
of BAY
86-9766 in
our ongoing Phase 1 study as a single agent in advanced cancer
patients with different tumor types and our Phase 1/2 study in
combination with sorafenib. Dosing in the MTD expansion cohorts
of both studies is ongoing.
HIV
We have developed multiple product candidates from our HIV
program including RDEA806, a non-nucleoside reverse
transcriptase inhibitor, or NNRTI, for the treatment of HIV,
which has successfully completed Phase 1 and Phase 2a studies
and has been evaluated in over 250 subjects. Results from a
Phase 2a monotherapy
proof-of-concept
study of RDEA806 demonstrated placebo-adjusted plasma viral load
reductions of up to 2.0 log10 on day 8 with once-daily dosing of
RDEA806. All dosing regimens tested were well tolerated in this
study.
We have also developed RDEA427, a next generation NNRTI, that is
from a chemical class that is distinct from the RDEA806 chemical
class. Based on preclinical results, RDEA427 demonstrates many
of the same positive attributes as RDEA806, but is more potent,
has superior pharmacokinetic properties, and has even greater
activity against a wide range of drug-resistant viral isolates,
than RDEA806. We have evaluated RDEA427 in a human micro-dose
pharmacokinetic study.
Further development of RDEA806 and RDEA427 will be dependent
upon our ability to partner this program.
Market Opportunity
We believe that there is a significant market opportunity for
our products, should they be successfully developed, approved
and commercialized.
We believe that there is a significant need for new products for
the treatment and prevention of gout. There have been only two
new products approved in the United States for the treatment of
gout in the last 40 years. According to the Decision
Resources, an
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estimated 19.7 million adults in the seven major markets
(the United States, Japan, France, Germany, Italy, Spain and
United Kingdom) suffer from gout. The incidence and severity of
gout is increasing in the United States. According to the Annals
of Rheumatic Diseases there was a 288% increase in gout-related
hospitalizations from
1988-2005
and over $11.2 billion in gout-related hospital costs were
incurred in 2005 in the United States. Many chronic gout
sufferers are unable to achieve target reductions in uric acid
with current treatments. Scientists have recently discovered
defects in multiple transporters in the kidney that play
important roles in uric acid transport and are genetically
linked to a higher risk of gout. URAT1 has been identified as
the most important transporter for uric acid. We are developing
products for the treatment of hyperuricemia and gout that
inhibit URAT1, thereby increasing the excretion of uric acid and
lowering serum uric acid levels. In addition, we believe there
may be opportunities to develop uric acid-lowering agents to
treat diseases other than gout. Evidence suggests that the
chronic elevation of uric acid associated with gout, known as
hyperuricemia, may also have systemic consequences, including an
increased risk for kidney dysfunction, elevated CRP,
hypertension and possibly other cardiovascular risk factors.
We also believe that there is growing interest in the potential
for targeted therapies, including kinase inhibitors, for the
treatment of both cancer and inflammatory disease. Sales of
products used in the treatment of cancer were $52.4 billion
in 2009 according to IMS Health Incorporated, fueled by strong
acceptance of innovative and effective targeted therapies. In
addition to cancer, MEK appears to play a role in inflammatory
diseases and we believe that BAY
86-9766 and
our next generation MEK inhibitors, if successfully developed,
approved and commercialized, could participate in these growing
markets.
In 2009, global sales of HIV antivirals were approximately
$13.8 billion. While the treatment of HIV has improved
dramatically over the past decade, we believe that there remains
a significant need for new treatments that are effective against
drug-resistant virus, safer for women and
African-Americans,
well tolerated and convenient to take. According to the Centers
for Disease Control and Prevention (CDC),
56,300 people were newly infected with HIV in 2006, 40%
more than estimated previously.
African-Americans
accounted for more than 45% of the new infections. Women account
for 27% of the new infections. We have developed products for
the treatment of HIV that are highly active against resistant
strains, have a high genetic barrier to resistance, have a
better safety profile than current drugs in
African-Americans
and women, can be taken once a day, and are easy to formulate in
a combination pill with current drugs. The further development
of these drugs will depend on our ability to partner the HIV
program.
Bayer
Relationship
Under the terms of our license agreement with Bayer, we granted
to Bayer a worldwide, exclusive license to develop and
commercialize our MEK inhibitors for all indications. In June
2009, Bayer paid us a non-refundable, upfront cash payment of
$35 million in partial consideration for the exclusive
right to develop and commercialize our MEK inhibitors. Potential
payments under the license agreement with Bayer could total up
to $407 million, not including royalties. This amount
includes the upfront cash payment, as well as additional cash
payments upon achievement of certain development, regulatory and
sales-based milestones. We are also eligible to receive low
double-digit royalties on sales of products under the license
agreement. We are responsible for the completion of the Phase 1
and Phase 1/2 studies currently being conducted for BAY
86-9766.
Valeant
Relationship
In December 2006, we acquired intellectual property and other
assets from Valeant Research & Development, Inc.
(Valeant) related to RDEA806 and our next generation
non-neucleoside reverse transcriptase inhibitor
(NNRTI) program, and BAY
86-9766 and
our next generation MEK inhibitor program. In consideration for
the assets purchased from Valeant and subject to the
satisfaction of certain conditions, Valeant received certain
rights, including the right to receive from us development-based
milestone payments and sales-based royalty payments. There is
one set of potential milestones totaling up to $25 million
for RDEA806 and the next generation NNRTI program, and a
separate set of potential milestones totaling up to
$17 million for BAY
86-9766 and
the next generation MEK inhibitor program. The first milestone
payments of $2 million and $1 million in the NNRTI
program and the MEK inhibitor program, respectively, would be
due after the first patient is dosed in the first Phase 2b
study. The royalty rates on all products are in the mid-single
digits.
Under the asset purchase agreement, Valeant retains a one-time
option to repurchase commercialization rights in territories
outside the United States and Canada for our first NNRTI product
derived from the acquired intellectual property to advance to a
Phase 2b HIV clinical trial. If Valeant exercises this option,
which it can do following the completion of a Phase 2b clinical
trial, but prior to the initiation of a Phase 3 clinical trial,
Valeant would pay us a $10 million option fee, up to
$21 million in milestone payments based on regulatory
approvals, and a mid-single-digit royalty on product sales in
the Valeant Territories.
We were incorporated in the State of Delaware in January 1994.
Our corporate offices are located at 4939 Directors Place,
San Diego, CA 92121. Our telephone number is
(858) 652-6500.
Our website address is www.ardeabio.com. We make available free
of charge through our Internet website our annual report on
Form 10-K,
quarterly reports on
Form 10-Q,
current reports on
Form 8-K,
and amendments to those reports filed or furnished pursuant to
Section 13(a) or 15(d) of the Securities Exchange Act of
1934, as amended, or the Exchange Act, as soon as reasonably
practicable after we electronically file such material with, or
furnish it to, the
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SEC. Information contained on our website, unless specifically
referenced herein, does not constitute part of this prospectus
or any prospectus supplement.
THE
SECURITIES WE MAY OFFER
We may offer shares of our common stock or warrants to purchase
shares of our common stock, either individually or in units,
with a total value of up to $100,000,000 from time to time under
this prospectus at prices and on terms to be determined at the
time of any offering. This prospectus provides you with a
general description of the securities we may offer. Each time we
offer a type or series of securities under this prospectus, we
will provide a prospectus supplement that will describe the
specific amounts, prices and other important terms of the
securities, including, to the extent applicable:
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aggregate offering price;
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redemption, exercise or exchange terms;
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restrictive covenants;
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voting or other rights;
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exchange or exercise prices or rates and, if applicable, any
provisions for changes to or adjustments in the exchange or
exercise prices or rates and in the securities or other property
receivable upon exchange or exercise; and
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a discussion of material United States federal income tax
considerations.
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The prospectus supplement and any related free writing
prospectus that we may authorize to be provided to you may also
add, update or change information contained in this prospectus
or in documents we have incorporated by reference. However, no
prospectus supplement or free writing prospectus will offer a
security that is not registered and described in this prospectus
at the time of the effectiveness of the registration statement
of which this prospectus is a part.
This prospectus may not be used to offer or sell securities
unless it is accompanied by a prospectus supplement.
We may sell the securities directly to investors or to or
through agents, underwriters or dealers. We and our agents,
underwriters and dealers reserve the right to accept or reject
all or part of any proposed purchase of securities. If we do
offer securities to or through agents, underwriters or dealers,
we will include in the applicable prospectus supplement:
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the names of those agents, underwriters or dealers;
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applicable fees, discounts and commissions to be paid to them;
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details regarding over-allotment options, if any; and
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the net proceeds to us.
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Common Stock. We may issue shares of our common
stock from time to time. Common stockholders are entitled to one
vote per share for the election of directors and on all other
matters that require common stockholder approval.
Subject to any preferential rights of any outstanding preferred
stock, in the event of our liquidation, dissolution or winding
up, holders of our common stock are entitled to share ratably in
the assets remaining after payment of liabilities and the
liquidation preferences of any outstanding preferred stock. Our
common stock does not carry any preemptive rights enabling a
holder to subscribe for, or receive shares of, any class of our
common stock or any other securities convertible into shares of
any class of our common stock, or any redemption rights.
Warrants. We may issue warrants for the purchase
of common stock in one or more series. We may issue warrants
independently or together with common stock and the warrants may
be attached to or separate from such common stock. In this
prospectus, we have summarized certain general features of the
warrants. We urge you, however, to read the applicable
prospectus supplement (and any free writing prospectus that we
may authorize to be provided to you) related to the series of
warrants being offered, as well as any warrant agreements and
warrant certificates that contain the terms of the warrants. We
will file as exhibits to the registration statement of which
this prospectus is a part, or will incorporate by reference from
reports that we file with the SEC, any forms of warrant
agreements and forms of warrant certificates containing the
terms of the warrants being offered, and any supplemental
warrant agreements and forms of warrant certificates containing
the terms of the warrants being offered.
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Any warrants issued under this prospectus may be evidenced by
warrant certificates. Warrants also may be issued under an
applicable warrant agreement that we enter into with a warrant
agent. We will indicate the name and address of the warrant
agent, if applicable, in the prospectus supplement relating to
the particular series of warrants being offered.
Units. We may issue, in one or more series, units
consisting of common stock and warrants for the purchase of
common stock. In this prospectus, we have summarized certain
general features of the units. We urge you, however, to read the
applicable prospectus supplement (and any free writing
prospectus that we may authorize to be provided to you) related
to the series of units being offered, as well as any unit
agreement that contains the terms of the units. We will file as
exhibits to the registration statement of which this prospectus
is a part, or will incorporate by reference from reports that we
file with the SEC, any form of unit agreement and any
supplemental agreements that describe the terms of the series of
units we are offering before the issuance of the related series
of units.
Any units issued under this prospectus may be evidenced by unit
certificates. Units also may be issued under an applicable unit
agreement that we enter into with a unit agent. We will indicate
the name and address of the unit agent, if applicable, in the
prospectus supplement relating to the particular series of units
being offered.
RISK
FACTORS
An investment in our securities involves a high degree of
risk. Before you make a decision to invest in our securities,
you should consider carefully the risks described in the section
entitled Risk Factors contained in our Annual Report
on
Form 10-K
for the fiscal year ended December 31, 2009, as filed with
the SEC on March 12, 2010, and our Quarterly Reports on
Form 10-Q
for the fiscal quarters ended March 31, 2010 and
June 30, 2010, as filed with the SEC on May 7, 2010
and August 6, 2010, respectively, each of which is
incorporated herein by reference in its entirety, as well as any
amendment or update thereto reflected in subsequent filings with
the SEC and any information in this prospectus or any
accompanying prospectus supplement. If any of these risks
actually occur, our business, operating results, prospects or
financial condition could be materially and adversely affected.
This could cause the trading price of our common stock, or if
applicable, other securities, to decline and you may lose part
or all of your investment. Moreover, the risks described are not
the only ones that we face. Additional risks not presently known
to us or that we currently deem immaterial may also affect our
business, operating results, prospects or financial
condition.
FORWARD-LOOKING
STATEMENTS
This prospectus, the documents that we incorporate by reference
herein and the applicable prospectus supplement contain
forward-looking statements within the meaning of
Section 27A of the Securities Act of 1933, as amended, or
the Securities Act, and Section 21E of the Exchange Act of
1934, as amended, or the Exchange Act. Any statements about our
expectations, beliefs, plans, objectives, assumptions or future
events or performance are not historical facts and may be
forward-looking. These statements are often, but not always,
made through the use of words or phrases such as anticipate,
estimate, plan, project, continuing, ongoing, goal, expect,
management believes, we believe, we intend and similar words or
phrases. Accordingly, these statements involve estimates,
assumptions and uncertainties that could cause actual results to
differ materially from those expressed in them. Any
forward-looking statements are qualified in their entirety by
reference to the factors discussed in this prospectus, in the
applicable prospectus supplement or incorporated by reference.
Because the factors discussed in this prospectus, incorporated
by reference herein or discussed in the applicable prospectus
supplement, and even factors of which we are not yet aware,
could cause actual results or outcomes to differ materially from
those expressed in any forward-looking statements made by or on
behalf of us, you should not place undue reliance on any such
forward-looking statements. These statements are subject to
risks and uncertainties, known and unknown, which could cause
actual results and developments to differ materially from those
expressed or implied in such statements. We have included
important factors in the cautionary statements included in this
prospectus, in the applicable prospectus supplement,
particularly under the heading RISK FACTORS, and in
our SEC filings that we believe could cause actual results or
events to differ materially from the forward-looking statements
that we make. These and other risks are also detailed in our
reports filed from time to time under the Securities Act
and/or the
Exchange Act. You are encouraged to read these filings as they
are made.
Further, any forward-looking statement speaks only as of the
date on which it is made, and we undertake no obligation to
update any forward-looking statement or statements to reflect
events or circumstances after the date on which such statement
is made or to reflect the occurrence of unanticipated events.
New factors emerge from time to time, and it is not possible for
us to predict which factors will arise. In addition, we cannot
assess the impact of each factor on our business or the extent
to which any factor, or combination of factors, may cause actual
results to differ materially from those contained in any
forward-looking statements.
5
DESCRIPTION
OF CAPITAL STOCK
As of the date of this prospectus, our certificate of
incorporation authorizes us to issue 70,000,000 shares of
common stock, par value $0.001 per share, and
5,000,000 shares of preferred stock, $0.001 par value
per share. As of October 21, 2010, 23,178,099 shares
of common stock were outstanding and no shares of preferred
stock were outstanding.
The following summary describes the material terms of our
capital stock and is qualified by reference to our certificate
of incorporation and our bylaws, which are incorporated by
reference as exhibits into the registration statement of which
this prospectus is a part.
Common
Stock
Voting. Common stockholders are entitled to one vote per
share for the election of directors and on all other matters
that require stockholder approval. Under our certificate of
incorporation and bylaws, directors are elected by a plurality
vote, and our stockholders do not have cumulative voting rights.
Accordingly, the holders of a majority of our outstanding shares
of common stock entitled to vote in any election of directors
can elect all of the directors standing for election, if they
should so choose. In all other matters, an action by our common
stockholders requires the affirmative vote of the holders of a
majority of our outstanding shares of common stock entitled to
vote.
Dividends and Other Distributions. Subject to the rights
of any outstanding shares of preferred stock, holders of our
common stock are entitled to share in an equal amount per share
in any dividends declared by our board of directors on the
common stock and paid out of legally available assets. Any
dividends on our common stock will be non-cumulative.
Distribution on Liquidation or Dissolution. In the event
of our liquidation, dissolution or winding up, holders of our
common stock are entitled to share ratably in all assets legally
available for distribution to our stockholders after the payment
of all of our debts and other liabilities and the satisfaction
of any liquidation preference granted to the holders of any
outstanding shares of our preferred stock.
Other Rights. Our common stock does not carry any
preemptive rights enabling a holder to subscribe for, or receive
shares of, any class of our common stock or any other securities
convertible into shares of any class of our common stock, or any
redemption rights.
Preferred
Stock
Under our certificate of incorporation, our board of directors
has the authority, without further action by stockholders, to
designate up to 5,000,000 shares of preferred stock in one
or more series and to fix or alter, from time to time, the
designations, powers and rights of each series of preferred
stock and the qualifications, limitations or restrictions of any
series of preferred stock, including dividend rights, dividend
rate, conversion rights, voting rights, rights and terms of
redemption (including sinking fund provisions), redemption price
or prices, and the liquidation preference of any wholly unissued
series of preferred stock, any or all of which may be greater
than the rights of the common stock, and to establish the number
of shares constituting any such series.
The issuance of preferred stock could adversely affect the
voting power of holders of common stock and reduce the
likelihood that common stockholders will receive dividend
payments and payments upon liquidation. The issuance could have
the effect of decreasing the market price of the common stock.
The issuance of preferred stock also could have the effect of
delaying, deterring or preventing a change in control of us.
Anti-Takeover
Provisions
Delaware Law. We are governed by the provisions of
Section 203 of the Delaware General Corporation Law. In
general, Section 203 prohibits a publicly held Delaware
corporation from engaging in a business combination
with an interested stockholder for a period of three
years after the date of the transaction in which the person
became an interested stockholder, unless (i) before the
date that the person became an interested
stockholder, our board of directors approved either the
business combination or the transaction which makes
the person an interested stockholder, (ii) the
interested stockholder owned at least 85% of the
voting stock of the corporation outstanding at the time the
transaction commenced, excluding for purposes of determining the
number of shares outstanding (a) shares owned by persons
who are directors and also officers and (b) shares owned by
employee stock plans in which employee participants do not have
the right to determine confidentially whether shares held
subject to the plan will be tendered in a tender or exchange
offer, or (iii) after the date that the person became an
interested stockholder, the business combination is
approved by our board of directors and the vote of at least 66
2/3% of our outstanding voting stock that is not owned by the
interested stockholder. Generally, a business
combination includes a merger, asset sale or other
transaction resulting in a
6
financial benefit to the stockholder. An interested
stockholder is a person who either owns 15% or more of our
outstanding voting stock or, together with affiliates and
associates, owns or, within three prior years, did own, 15% or
more of our outstanding voting stock. The statute could have the
effect of delaying, deferring or preventing a change in our
control.
Bylaws and Certificate of Incorporation Provisions. Our
certificate of incorporation and bylaws include a number of
provisions that may have the effect of deterring hostile
takeovers or delaying or preventing changes in our control or
our managements, including, but not limited to the following:
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Our board of directors can issue up to 5,000,000 shares of
preferred stock with any rights or preferences, including the
right to approve or not approve an acquisition or change in our
control.
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Our certificate of incorporation and bylaws provide that all
stockholder actions must be effected at a duly called meeting of
holders and not by written consent.
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Our bylaws provide that special meetings of our stockholders may
be called only by the Chairman of our board of directors, our
Chief Executive Officer, or by our board of directors pursuant
to a resolution adopted by a majority of the total number of
authorized directors.
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Our bylaws provide that stockholders seeking to present
proposals before a meeting of stockholders or to nominate
candidates for election as directors at a meeting of
stockholders must provide timely notice in writing and also
specify requirements as to the form and content of a
stockholders notice. These provisions may delay or
preclude stockholders from bringing matters before a meeting of
our stockholders or from making nominations for directors at a
meeting of stockholders, which could delay or deter takeover
attempts or changes in our management.
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Our certificate of incorporation and bylaws provide that,
subject to the rights of the holders of any outstanding series
of preferred stock, all vacancies, including newly created
directorships, may, except as otherwise required by law, be
filled by the affirmative vote of a majority of directors then
in office. Our certificate of incorporation provides that the
authorized number of directors must be set within a range of
five to eleven pursuant to a resolution adopted by a majority of
the directors then in office.
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Our certificate of incorporation does not include a provision
for cumulative voting for directors. Under cumulative voting, a
minority stockholder holding a sufficient percentage of a class
of shares could be able to ensure the election of one or more
directors.
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Transfer
Agent and Registrar
The transfer agent and registrar for our common stock is
ComputerShare Trust Company, N.A.
Listing
on The NASDAQ Global Market
Our common stock is listed on The NASDAQ Global Market under the
symbol RDEA.
DESCRIPTION
OF WARRANTS
We may issue warrants for the purchase of common stock in one or
more series. We may issue warrants independently or together
with common stock and the warrants may be attached to or
separate from such common stock. While the terms summarized
below will apply generally to any warrants that we may offer, we
will describe the particular terms of any series of warrants in
more detail in the applicable prospectus supplement. The terms
of any warrants offered under a prospectus supplement may differ
from the terms described below.
We have filed the form of the warrant agreement and the form of
the warrant certificate containing the terms of the warrants
being offered as exhibits to the registration statement of which
this prospectus is a part. We will file as exhibits to the
registration statement of which this prospectus is a part, or
will incorporate by reference from reports that we file with the
SEC, the form of warrant agreement, including a form of warrant
certificate, that describes the terms of the particular series
of warrants we are offering before the issuance of the related
series of warrants. The following summaries of material
provisions of the warrants and the warrant agreement are subject
to, and qualified in their entirety by reference to, all of the
provisions of the warrant agreement and warrant certificate
applicable to the particular series of warrants that we may
offer under this prospectus. We urge you to read the applicable
prospectus supplements related to the particular series of
warrants that we may offer under this prospectus, as well as any
free writing
7
prospectuses that we may authorize to be provided to you in
connection with the warrants, and the complete warrant agreement
and warrant certificate that contain the terms of the warrants.
General
We will describe in the applicable prospectus supplement the
terms of the series of warrants being offered, including, to the
extent applicable:
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the offering price and aggregate number of warrants offered;
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the currency for which the warrants may be purchased;
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the date on and after which the warrants and the related
securities will be separately transferable;
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the number of shares of common stock purchasable upon the
exercise of one warrant and the price at which these shares may
be purchased upon such exercise;
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the effect of any merger, consolidation, sale or other
disposition of our business on the warrant agreements and the
warrants;
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the terms of any rights to redeem or call the warrants;
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any provisions for changes to or adjustments in the exercise
price or number of shares of common stock issuable upon exercise
of the warrants;
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the dates on which the right to exercise the warrants will
commence and expire;
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the manner in which the warrant agreement and warrants may be
modified;
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a discussion of material United States federal income tax
consequences of holding or exercising the warrants; and
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any other specific terms, preferences, rights or limitations of
or restrictions on the warrants.
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Before exercising their warrants, holders of warrants will not
have any of the rights of holders of common stock purchasable
upon such exercise, including the right to receive dividends, if
any, or, payments upon our liquidation, dissolution or winding
up or to exercise voting rights, if any.
Exercise
of Warrants
Each warrant will entitle the holder to purchase shares of our
common stock at the exercise price that we describe in the
applicable prospectus supplement. Unless we otherwise specify in
the applicable prospectus supplement, holders of the warrants
may exercise the warrants at any time up to the specified time
on the expiration date that we set forth in the applicable
prospectus supplement. After the close of business on the
expiration date, unexercised warrants will become void.
Holders of the warrants may exercise the warrants by delivering
the warrant or warrant certificate representing the warrants to
be exercised together with specified information, and paying the
required amount to the warrant agent, if applicable, in
immediately available funds, as provided in the applicable
prospectus supplement. We will set forth on the reverse side of
any warrant certificate and in the applicable prospectus
supplement the information that the holder of the warrant will
be required to deliver to any warrant agent.
Upon receipt of the required payment and any warrant certificate
properly completed and duly executed at the corporate trust
office of any warrant agent or any other office indicated in the
applicable prospectus supplement, we will issue and deliver the
shares of common stock purchasable upon such exercise. If fewer
than all of the warrants represented by a warrant certificate
are exercised, then we will issue a new warrant certificate for
the remaining amount of warrants. If we so indicate in the
applicable prospectus supplement, holders of the warrants may
surrender securities as all or part of the exercise price for
warrants.
Governing
Law
Unless we provide otherwise in the applicable prospectus
supplement, the warrants and warrant agreement will be governed
by and construed in accordance with the laws of the State of New
York.
8
Enforceability
of Rights by Holders of Warrants
Any warrant agent will act solely as our agent under the
applicable warrant agreement and will not assume any obligation
or relationship of agency or trust with any holder of any
warrant. A single bank or trust company may act as warrant agent
for more than one series of warrants. A warrant agent will have
no duty or responsibility in case of any default by us under the
applicable warrant agreement or warrant, including any duty or
responsibility to initiate any proceedings at law or otherwise,
or to make any demand upon us. Any holder of a warrant may,
without the consent of any related warrant agent or the holder
of any other warrant, enforce by appropriate legal action its
right to exercise, and receive the securities purchasable upon
exercise of, its warrants.
DESCRIPTION
OF UNITS
We may issue, in one more series, units consisting of common
stock and warrants for the purchase of common stock. While the
terms we have summarized below will apply generally to any units
that we may offer under this prospectus, we will describe the
particular terms of any series of units in more detail in the
applicable prospectus supplement. The terms of any units offered
under a prospectus supplement may differ from the terms
described below.
We will file as exhibits to the registration statement of which
this prospectus is a part, or will incorporate by reference from
reports that we file with the SEC, any form of unit agreement
that describes the terms of the series of units we are offering,
and any supplemental agreements. The following summaries of
material terms and provisions of the units are subject to, and
qualified in their entirety by reference to, all of the
provisions of any unit agreement and any supplemental agreements
applicable to a particular series of units. We urge you to read
the applicable prospectus supplements related to the particular
series of units that we may offer under this prospectus, as well
as any free writing prospectuses that we may authorize to be
provided to you in connection with the units and any unit
agreement and any supplemental agreements that contain the terms
of the units.
General
Each unit will be issued so that the holder of the unit is also
the holder of each security included in the unit. Thus, the
holder of a unit will have the rights and obligations of a
holder of each included security. Any unit agreement under which
a unit is issued may provide that the securities included in the
unit may not be held or transferred separately, at any time or
at any time before a specified date.
We will describe in the applicable prospectus supplement the
terms of the series of units being offered, including, to the
extent applicable:
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the designation and terms of the units and of the securities
comprising the units, including whether and under what
circumstances those securities may be held or transferred
separately;
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any provisions of the governing unit agreement that differ from
those described below; and
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any provisions for the issuance, payment, settlement, transfer
or exchange of the units or of the securities comprising the
units.
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The provisions described in this section, as well as those
described under Description of Capital Stock and
Description of Warrants will apply to each unit and
to any common stock or warrant included in each unit,
respectively.
Issuance
in Series
We may issue units in such amounts and in such number of
distinct series as we determine.
Enforceability
of Rights by Holders of Units
Any unit agent will act solely as our agent under the applicable
unit agreement and will not assume any obligation or
relationship of agency or trust with any holder of any unit. A
single bank or trust company may act as unit agent for more than
one series of units. A unit agent will have no duty or
responsibility in case of any default by us under the applicable
unit agreement or unit, including any duty or responsibility to
initiate any proceedings at law or otherwise, or to make any
demand upon us. Any holder of a unit may, without the consent of
any related unit agent or the holder of any other unit, enforce
by appropriate legal action its rights as holder under any
security included in the unit.
9
Title
We and any unit agent and any of their agents may treat the
registered holder of any unit certificate as an absolute owner
of the units evidenced by that certificate for any purpose and
as the person entitled to exercise the rights attaching to the
units so requested, despite any notice to the contrary.
USE OF
PROCEEDS
Except as described in any prospectus supplement, we currently
intend to use the net proceeds from the sale of the securities
offered hereby to fund the costs of clinical trial and other
research and development activities and for general corporate
purposes, including working capital. We may also use a portion
of the net proceeds to in-license, invest in or acquire
businesses or technologies that we believe are complementary to
our own, although we have no current plans, commitments or
agreements with respect to any acquisitions as of the date of
this prospectus. Pending these uses, we intend to invest the net
proceeds in investment-grade, interest-bearing securities.
PLAN OF
DISTRIBUTION
We may sell our securities covered by this prospectus in any of
three ways (or in any combination):
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to or through underwriters or dealers;
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directly to one or more purchasers; or
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through agents.
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We may distribute the securities:
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from time to time in one or more transactions at a fixed price
or prices, which may be changed from time to time;
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at market prices prevailing at the time of sale;
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at prices related to the prevailing market prices; or
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at negotiated prices.
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Each time we offer and sell securities covered by this
prospectus, we will provide a prospectus supplement or
supplements that will describe the method of distribution and
set forth the terms of the offering, including:
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the name or names of any underwriters, dealers or agents;
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the amounts of securities underwritten or purchased by each of
them;
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the purchase price of the securities and the proceeds we will
receive from the sale;
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any over-allotment options under which underwriters may purchase
additional common stock from us;
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any underwriting discounts or commissions or agency fees and
other items constituting underwriters or agents
compensation;
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the public offering price of the securities;
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any discounts, commissions or concessions allowed or reallowed
or paid to dealers; and
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any securities exchange or market on which the common stock may
be listed.
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Any public offering price and any discounts or concessions
allowed or reallowed or paid to dealers may be changed from time
to time. We may determine the price or other terms of the
securities offered under this prospectus by use of an electronic
auction. We will describe how any auction will determine the
price or any other terms, how potential investors may
participate in the auction and the nature of the obligations of
the underwriter, dealer or agent in the applicable prospectus
supplement.
10
Underwriters or dealers may offer and sell the offered
securities from time to time in one or more transactions,
including negotiated transactions, at a fixed public offering
price or at varying prices determined at the time of sale. If
underwriters or dealers are used in the sale of any securities,
the securities will be acquired by the underwriters or dealers
for their own account and may be resold from time to time in one
or more transactions described above. The securities may be
either offered to the public through underwriting syndicates
represented by managing underwriters, or directly by
underwriters or dealers. Generally, the underwriters or
dealers obligations to purchase the securities will be
subject to certain conditions precedent. The underwriters or
dealers will be obligated to purchase all of the securities if
they purchase any of the securities, unless otherwise specified
in the prospectus supplement. We may use underwriters with whom
we have a material relationship. We will describe the nature of
any such relationship in the prospectus supplement, naming the
underwriter.
We may sell the securities through agents from time to time. The
prospectus supplement will name any agent involved in the offer
or sale of the securities and any commissions we pay to them.
Generally, any agent will be acting on a best efforts basis for
the period of its appointment. We may authorize underwriters,
dealers or agents to solicit offers by certain purchasers to
purchase the securities from us at the public offering price set
forth in the prospectus supplement pursuant to delayed delivery
contracts providing for payment and delivery on a specified date
in the future. The contracts will be subject only to those
conditions set forth in the prospectus supplement, and the
prospectus supplement will set forth any commissions we pay for
solicitation of these contracts.
Agents, dealers and underwriters may be entitled to
indemnification by us against certain civil liabilities,
including liabilities under the Securities Act, or to
contribution with respect to payments which the agents, dealers
or underwriters may be required to make in respect thereof.
Agents, dealers and underwriters may be customers of, engage in
transactions with, or perform services for us in the ordinary
course of business.
All securities we may offer, other than common stock, will be
new issues of securities with no established trading market. Any
underwriters may make a market in these securities, but will not
be obligated to do so and may discontinue any market making at
any time without notice. We cannot guarantee the liquidity of
the trading markets for any securities.
Any underwriter may engage in over-allotment, stabilizing
transactions, short covering transactions and penalty bids in
accordance with Regulation M under the Exchange Act.
Over-allotment involves sales in excess of the offering size,
which create a short position. This short sales position may
involve either covered short sales or
naked short sales. Covered short sales are short
sales made in an amount not greater than the underwriters
over-allotment option to purchase additional securities in this
offering described above. The underwriters may close out any
covered short position either by exercising their over-allotment
option or by purchasing securities in the open market. To
determine how they will close the covered short position, the
underwriters will consider, among other things, the price of
securities available for purchase in the open market, as
compared to the price at which they may purchase securities
through the over-allotment option. Naked short sales are short
sales in excess of the over-allotment option. The underwriters
must close out any naked short position by purchasing securities
in the open market. A naked short position is more likely to be
created if the underwriters are concerned that, in the open
market after pricing, there may be downward pressure on the
price of the securities that could adversely affect investors
who purchase securities in this offering. Stabilizing
transactions permit bids to purchase the underlying security for
the purpose of fixing the price of the security so long as the
stabilizing bids do not exceed a specified maximum. Penalty bids
permit the underwriters to reclaim a selling concession from a
dealer when the securities originally sold by the dealer are
purchased in a covering transaction to cover short positions.
Similar to other purchase transactions, an underwriters
purchase to cover the syndicate short sales or to stabilize the
market price of our securities may have the effect of raising or
maintaining the market price of our securities or preventing or
mitigating a decline in the market price of our securities. As a
result, the price of our securities may be higher than the price
that might otherwise exist in the open market. The imposition of
a penalty bid might also have an effect on the price of the
securities if it discourages resales of the securities.
Neither we nor the underwriters makes any representation or
prediction as to the effect that the transactions described
above may have on the price of the securities. If such
transactions are commenced, they may be discontinued without
notice at any time.
LEGAL
MATTERS
The validity of the securities offered by this prospectus will
be passed upon for us by Cooley LLP, San Diego, California.
EXPERTS
Stonefield Josephson, Inc., independent registered public
accounting firm, has audited our consolidated financial
statements as of and for the year ended December 31, 2009
and the effectiveness of Ardea Biosciences, Inc.s internal
control over financial reporting as of December 31, 2009,
as set forth in their reports, each of which are included in our
Annual Report on
Form 10-K
for the year ended December 31, 2009 as filed with the SEC
on March 12, 2010, and are incorporated by reference in
this prospectus and
11
elsewhere in the registration statement. These financial
statements are incorporated by reference in reliance on
Stonefield Josephson, Inc.s reports, given on their
authority as experts in accounting and auditing.
WHERE YOU
CAN FIND MORE INFORMATION
We are a reporting company and file annual, quarterly and
current reports, proxy statements and other information with the
Securities and Exchange Commission, or the SEC. You may read and
copy these reports, proxy statements and other information at
the SECs public reference room at 100 F Street,
N.E., Washington, D.C. 20549 or at the SECs other
public reference facilities. Please call the SEC at
1-800-SEC-0330
for more information about the operation of the public reference
room. You can request copies of these documents by writing to
the SEC and paying a fee for the copying costs. Our SEC filings
are also available at the SECs website at
http://www.sec.gov.
This prospectus is part of a registration statement that we
filed with the SEC. The registration statement contains more
information than this prospectus regarding us and our common
stock, including certain exhibits and schedules. You can obtain
a copy of the registration statement from the SEC at the address
listed above or from the SECs internet website.
INCORPORATION
OF CERTAIN INFORMATION BY REFERENCE
We are allowed to incorporate by reference information contained
in documents that we file with the SEC. This means that we can
disclose important information to you by referring you to those
documents and that the information in this prospectus is not
complete. You should read the information incorporated by
reference for more detail. We incorporate by reference in two
ways. First, we list certain documents that we have already
filed with the SEC. The information in these documents is
considered part of this prospectus. Second, the information in
documents that we file in the future will update and supersede
the current information in, and incorporated by reference in,
this prospectus.
We incorporate by reference the documents listed below and any
filings we will make with the SEC under Section 13(a),
13(c), 14 or 15(d) of the Exchange Act after the date we filed
the initial registration statement of which this prospectus is a
part and before the effective date of the registration statement
and any future filings we will make with the SEC pursuant to
Section 13(a), 13(c), 14 or 15(d) of the Exchange Act from
the date of this prospectus but prior to the termination of the
offering (in each case, except for the information in any of the
foregoing Current Reports on
Form 8-K
and
Form 8-K/A
furnished under Item 2.02 or Item 7.01 therein):
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Annual report on
Form 10-K
for the year ended December 31, 2009, filed with the SEC on
March 12, 2010 (including information specifically
incorporated by reference into our
Form 10-K
from our Proxy Statement for our 2010 Annual Meeting of
Stockholders);
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Quarterly report on
Form 10-Q
for the quarter ended March 31, 2010, filed with the SEC on
May 7, 2010;
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Quarterly report on
Form 10-Q
for the quarter ended June 30, 2010, filed with the SEC on
August 6, 2010;
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Current reports on
Form 8-K
filed with the SEC on February 9, 2010, March 8, 2010,
April 5, 2010, April 9, 2010, May 27, 2010,
September 17, 2010 and October 7, 2010 (except for the
information in such reports that shall not be deemed
filed for purposes of Section 18 of the
Exchange Act); and
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You may request a copy of these filings at no cost, by writing
or telephoning us at the following address or telephone number:
Ardea Biosciences, Inc.
4939 Directors Place
San Diego, CA 92121
Attn: Investor Relations
(858) 652-6500
This prospectus is part of a registration statement that we
filed with the SEC. The registration statement contains more
information than this prospectus regarding us and our common
stock, including certain exhibits and schedules. You can obtain
a copy of the registration statement from the SEC at the address
listed above or from the SECs internet website. You should
rely only on the information incorporated by reference or
provided in this prospectus or any prospectus supplement. We
have not authorized anyone else to provide you with different
information. You should not assume that the information in this
prospectus or any prospectus supplement is accurate as of any
date other than the date on the front of these documents.
12
2,750,000 Shares
Common Stock
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BofA
Merrill Lynch |
Jefferies |
JMP Securities
Brean Murray, Carret &
Co.
Roth Capital Partners
January 20, 2011