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As filed with the Securities and Exchange Commission on November 20, 2008
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Registration No. 333-155265 |
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
Amendment No. 1
to
FORM S-3
REGISTRATION STATEMENT UNDER
THE SECURITIES ACT OF 1933
Repros Therapeutics Inc.
(Exact name of registrant as specified in its charter)
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Delaware
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2834
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76-0233274 |
(State or other jurisdiction of
incorporation or organization)
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(Primary Standard Industrial
Classification Code Number)
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(I.R.S. Employer
Identification Number) |
2408 Timberloch Place, Suite B-7
The Woodlands, TX 77380
(281) 719-3400
(Address, including zip code,
and telephone
number, including
area code, of registrants
principal executive offices)
Joseph S. Podolski
President and Chief Executive Officer
Repros Therapeutics Inc.
2408 Timberloch Place, Suite B-7
The Woodlands, TX 77380
(281) 719-3400
(Name, address, including zip code, and telephone number, including area code, of agent for service)
Copies to:
Paul D. Aubert, Esq.
Winstead PC
24 Waterway Avenue, Suite 500
The Woodlands, TX 77380
(281) 681-5900
Approximate date of commencement of proposed sale to the public:
From time to time after the effective date of this Registration Statement.
If the only securities being registered on this form are being offered pursuant to dividend or
interest reinvestment plans, please check the following box. o
If any of the securities being registered on this form are to be offered on a delayed or
continuous basis pursuant to Rule 415 under the Securities Act of 1933, other than securities
offered only in connection with dividend or interest reinvestment plans, check the following box.
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If this form is filed to register additional securities for an offering pursuant to
Rule 462(b) under the Securities Act, check the following box and list the Securities Act
registration statement number of the earlier effective registration statement for the same
offering. o
If this form is a post-effective amendment filed pursuant to Rule 462(c) under the Securities
Act, check the following box and list the Securities Act registration statement number of the
earlier effective registration statement for the same offering. o
If this form is a registration statement pursuant to General Instruction I.D. or a
post-effective amendment thereto that shall become effective upon filing with the Commission
pursuant to Rule 462(e) under the Securities Act, check the following box. o
If this form is a post-effective amendment to a registration statement filed pursuant to
General Instruction I.D. filed to register additional securities or additional classes of
securities pursuant to Rule 413(b) under the Securities Act, check the following box. o
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated
filer, a non-accelerated filer, or a smaller reporting company. See the definitions of large
accelerated filer, accelerated filer and smaller reporting company in Rule 12b-2 of the
Exchange Act. (Check one):
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Large accelerated filer o
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Accelerated filer þ
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Non-accelerated filer o
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Smaller reporting company o |
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(Do not check if a smaller reporting company) |
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CALCULATION OF REGISTRATION FEE
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Proposed Maximum |
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Proposed Maximum |
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Amount to be |
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Offering Price Per |
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Aggregate Offering |
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Amount of Registration |
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Title of Each Class of Securities to be Registered |
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Registered |
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Share (1) |
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Price(1) |
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Fee(1) |
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Primary Offering: Common Stock, par value $.001 per share |
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5,000,000 |
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$9.14 |
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$45,700,000 |
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$1,800 |
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Secondary Offering: Common Stock, par value $.001 per share
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1,282,052 |
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$9.14 |
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$11,720,000 |
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$ 460 |
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Total |
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6,282,052(2) |
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$57,420,000 |
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$2,260(3) |
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(1) |
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Estimated solely for the purpose of calculating the registration fee pursuant to Rule 457(c)
under the Securities Act and based on the average high and low prices per share of common
stock on November 5, 2008 as reported on the Nasdaq Global Market. |
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Of this amount, all of the 1,282,052 shares issuable upon exercise of certain option rights
are authorized, but only 1,533,153 out of the 5,000,000 remaining shares are currently
authorized by the Registrants Restated Certificate of Incorporation, as amended. In order to
authorize such shares, the Registrant filed a definitive proxy statement on November 3, 2008
relating to a special meeting of its stockholders to be held on December 16, 2008 to approve
an amendment to the Restated Certificate of Incorporation, as amended, to increase the number
of authorized shares of the Registrants Common Stock from 20 million to 30 million. |
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(3) |
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Previously paid with the initial filing. |
The Registrant hereby amends this Registration Statement on such date or dates as may be
necessary to delay its effective date until the Registrant shall file a further amendment that
specifically states that this Registration Statement shall thereafter become effective in
accordance with Section 8(a) of the Securities Act of 1933 or until the Registration Statement
shall become effective on such date as the Securities and Exchange Commission, acting pursuant to
said Section 8(a), may determine.
PROSPECTUS
Up to 6,282,052 Shares of
Common Stock
From time to time, we may sell up to an aggregate of 5,000,000 shares of common stock in one
or more offerings, and certain selling stockholders may offer and sell up to 1,282,052 shares of
common stock issuable upon exercise of certain option rights granted to such selling stockholders.
This means:
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we will provide this prospectus and a prospectus supplement each time we sell the common stock; |
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the prospectus supplement will inform you about the specific terms of that offering and may also add, update or change
information contained in this prospectus; and
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you should read this prospectus and any prospectus supplement, as well as any documents incorporated by reference in
this prospectus and any prospectus supplement, carefully before you invest in our common stock. |
Our common stock is quoted on the Nasdaq Global Market under the trading symbol RPRX. On
November 18, 2008, the last reported sale price of our common stock on the Nasdaq Global Market was
$9.73 per share.
THIS PROSPECTUS MAY NOT BE USED TO OFFER OR SELL ANY SECURITIES UNLESS ACCOMPANIED BY A
PROSPECTUS SUPPLEMENT.
The common stock may be sold directly by us to purchasers, to or through underwriters or
dealers designated from time to time, or through agents designated from time to time. For
additional information on the methods of sale, you should refer to Plan of Distribution in this
prospectus and to the accompanying prospectus supplement. If any underwriters are involved in a
sale of the common stock, their names and any applicable commissions or discounts will be set forth
in a prospectus supplement. The net proceeds we expect to receive from the sale will also be set
forth in a prospectus supplement.
The selling shareholders may offer and sell any of the shares of common stock from time to
time at fixed prices, at market prices or at negotiated prices, and may engage a broker, dealer or
underwriter to sell the shares. For additional information on the possible methods of sale that may
be used by the selling shareholders, you should refer to the section entitled Plan of
Distribution beginning on page 8 of this prospectus. We will not receive any proceeds from the
sale of the shares of common stock by the selling shareholders. We will pay all expenses incurred
in effecting the registration statement of which this prospectus constitutes a part.
NEITHER THE SECURITIES AND EXCHANGE COMMISSION 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.
INVESTING IN OUR SECURITIES INVOLVES A HIGH DEGREE OF RISK. YOU SHOULD CAREFULLY CONSIDER THE
RISK FACTORS CONTAINED IN OUR ANNUAL REPORT ON FORM 10-K FOR THE FISCAL YEAR ENDED
DECEMBER 31,
2007, UPDATES IN PART II, ITEM 1A OF OUR FORM 10-Q FILINGS, AND IN OUR FUTURE FILINGS MADE WITH THE
SECURITIES AND EXCHANGE COMMISSION, WHICH ARE INCORPORATED BY REFERENCE IN THIS PROSPECTUS. SEE
THE SECTION ENTITLED RISK FACTORS ON PAGE 4 OF THIS PROSPECTUS.
The date of this prospectus is November 20, 2008
Table of Contents
We have not authorized any dealer, salesman or other person to give any information or to make
any representation other than those contained or incorporated by reference in this prospectus and
the accompanying supplement to this prospectus. You must not rely upon any information or
representation not contained or incorporated by reference in this prospectus or the accompanying
prospectus supplement. This prospectus and the accompanying supplement to this prospectus do not
constitute an offer to sell or the solicitation of an offer to buy common stock, nor do this
prospectus and the accompanying supplement to this prospectus constitute an offer to sell or the
solicitation of an offer to buy common stock in any jurisdiction to any person to whom it is
unlawful to make such offer or solicitation in such jurisdiction. You should not assume that the
information contained in this prospectus and the accompanying prospectus supplement is accurate on
any date subsequent to the date set forth on the front of the document or that any information we
have incorporated by reference is correct on any date subsequent to the date of the document
incorporated by reference, even though this prospectus and any accompanying prospectus supplement
is delivered or common stock sold on a later date.
ABOUT THIS PROSPECTUS
This prospectus is part of a registration statement that we filed with the Securities and
Exchange Commission using a shelf registration process. Under this shelf registration process, we
may sell common stock in one or more offerings, up to an aggregate number of 5,000,000 shares. In
addition, certain selling stockholders may offer to sell up to 1,282,052 shares of common stock
issuable upon exercise of certain option rights held by such selling stockholders.
This prospectus provides you with a general description of the securities we may offer. Each
time we sell common stock, 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 the prospectus
supplement any of the information contained in this prospectus. This prospectus, together with
applicable prospectus supplements, includes all material information relating to this offering. If
there is any inconsistency between the information in this prospectus and the information in the
accompanying prospectus supplement, you should rely on the information in the prospectus
supplement.
Please carefully read both this prospectus and any prospectus supplement together with the
additional information described below under Where You Can Find More Information.
Unless otherwise mentioned or unless the context requires otherwise, all references in this
prospectus to Repros, we, us, our or similar references mean Repros Therapeutics Inc.
ABOUT REPROS THERAPEUTICS INC.
Overview
Repros Therapeutics Inc. (the Company, or we, us or our), was organized on August 28,
1987. We are a development stage biopharmaceutical company focused on the development of oral small
molecule drugs to treat male and female reproductive disorders.
Our current product pipeline consists of the following (with the respective status of
development):
Proellex® (female reproductive health)
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Phase 3 three-month short course treatment of symptomatic uterine fibroids
associated with anemia in women who may consider having a subsequent hysterectomy |
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Phase 3 for the chronic treatment of symptomatic uterine fibroids |
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Phase 2 for the treatment of symptomatic endometriosis |
Androxal® (male reproductive health)
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Phase 2b proof-of-concept trial in men with low testosterone levels wanting to
improve or maintain their fertility and/or sperm number and function |
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Request pre-IND meeting with the Food and Drug Administrations, or FDAs,
Division of Metabolic and Endocrine Products to investigate Androxal as a treatment for
type 2 diabetes |
Proellex
Our lead drug, Proellex, is a selective progesterone receptor modulator (PRM) and is being
developed for the treatment of symptoms associated with uterine fibroids and endometriosis. We are
also developing Proellex as a short course pre-surgical treatment for anemia associated with
excessive menstrual bleeding related to uterine fibroids. During the first quarter of 2008, we
filed an Investigational New Drug Application, or IND, for Proellex for the treatment of anemia
associated with uterine fibroids and also initiated two 65-patient Phase 3 pivotal clinical trials
with Proellex for this indication. Our goal is to file a New Drug Application, or NDA, for this
indication in late 2009.
During the first quarter of 2008, we initiated two 75-patient Phase 3 pivotal clinical trials
with Proellex for the chronic treatment of uterine fibroids and anticipate filing a NDA for this
indication in late 2010. In addition, during the first quarter
of 2008, we also initiated two 400 patient Proellex Open Label Safety Studies. We intend to
complete patient enrollment for one 400 patient Open Label Safety Study then start enrollment in
the second Open Label Safety study.
The initiation of these Phase 3 clinical trials and Open Label Studies included awarding the
trials to three clinical research organizations, the process of identifying and contracting the
clinical sites to be used as well as other various activities required to complete these clinical
trials. During the second quarter of 2008, we implemented a centralized patient recruitment
advertising campaign for our Phase 3 Proellex clinical trials and in July 2008 we took the
necessary steps to begin additional patient recruitment advertising for one of our 400 patient
Proellex Open Label Safety Studies.
During 2008 we disclosed the following clinical trial and animal safety data relating to
Proellex:
initial results from 13 women who had endometrial biopsies post menses following last dose
of drug in a two drug cycle extension study showed that results of assessments of the post menses
tissues are that of a benign endometrium. While previous end of drug cycle biopsies from these
subjects all had histological changes consistent with those induced by progesterone receptor
modulators (Proellex class of drugs), none of these post drug cessation biopsies reflected any of
those histological changes. These key findings indicate that the effects of Proellex on the
endometrium are present during drug exposure and are reversible upon cessation of drug treatment;
results from a pilot study of the potential for adverse cardiac events associated with
administration of doses of Proellex up to four times higher than the intended marketed dose showed
that despite up to a four fold increase in Proellex plasma concentrations over seven days the QTc
did not change; and
initial macroscopic findings from a two-year rat carcinogenicity study and a six-month mouse
carcinogenicity study showed no potential for tumor induction as compared to placebo.
We are also currently conducting a Phase 2 clinical trial with Proellex for the treatment of
endometriosis. We provided initial interim data from this trial in July 2008 which showed that
severe pain, the most troublesome symptom associated with endometriosis, was significantly reduced
in one to two months of treatment. We intend to file a NDA for this indication in late 2010.
Uterine fibroids, anemia associated with uterine fibroids and endometriosis affect a
significant number of women of childbearing age in the developed world. There is no
currently-approved effective long-term drug treatment for uterine fibroids or endometriosis. In
the United States alone, 300,000 women per year undergo a hysterectomy as a result of severe
uterine fibroids.
In addition to the clinical trials discussed above we are also conducting additional human
clinical trials and animal safety studies with Proellex to support our future NDA submissions.
Androxal
Our second product candidate, Androxal, is a single isomer of clomiphene citrate and is an
orally active proprietary small molecule compound.
During the second quarter of 2008, we initiated a Phase 2b proof-of-concept Androxal clinical
trial in men of reproductive age with low testosterone levels who want to improve or maintain their
fertility and/or sperm function while being treated for low testosterone. This trial includes a
control group that will be given Testim®, a popular testosterone replacement therapy. We believe
Androxal will be superior to the existing drugs used to normalize testosterone as, to our
knowledge, only Androxal has the property of restoring both luteinizing hormone, or LH, and
follicle stimulating hormone, or FSH, levels. LH and FSH are the pituitary hormones that stimulate
testicular testosterone and sperm production, respectively. We intend to have an End of Phase 2
Meeting with the FDA in the second half of 2009. According to the Urology Channel, recent
estimates show that approximately 13 million men in the United States experience testosterone
deficiency.
In November 2008, we received guidance from the FDA suggesting submission of a new IND to the
Division of Metabolic and Endocrine Products, or DMEP, for the investigation of Androxal as a
potential treatment for type 2 diabetes. We plan to submit a new IND for this indication to the
DMEP as soon as practicable.
In addition to the clinical trials discussed above, we are also conducting a long-term Open
Label Safety Study and animal safety study with Androxal to support our future NDA submissions.
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We were previously developing Androxal in the United States to treat testosterone deficiency
due to secondary hypogonadism by restoring normal testosterone production in males with functional
testes and diminished pituitary function, a common condition in the aging male. Based on a Type
C meeting held with the FDA on October 15, 2007 we do not believe we have a clear clinical path
to develop Androxal for this indication in the United States at this time. Although we believe
Androxal could be developed outside of the United States, due to the limited European market for
this indication and our limited internal resources we do not intend to pursue approval outside of
the United States at this time.
Other Programs
We continue to maintain our patent portfolio of our phentolamine-based products for the
treatment of sexual dysfunction. However, no R&D investments are being made in these programs at
this time.
General
The clinical development of pharmaceutical products is a complex undertaking, and many
products that begin the clinical development process do not obtain regulatory approval. The costs
associated with our clinical trials may be impacted by a number of internal and external factors,
including the number and complexity of clinical trials necessary to obtain regulatory approval, the
number of eligible patients necessary to complete our clinical trials and any difficulty in
enrolling these patients, and the length of time to complete our clinical trials. Given the
uncertainty of these potential costs, we recognize that the total costs we will incur for the
clinical development of our product candidates may exceed our current estimates. We do, however,
expect these costs to increase substantially in future periods as we continue later-stage clinical
development trials. Any failure by us to obtain, or any delay in obtaining, regulatory approvals
could cause our research and development expenditures to increase and, in turn, have a material
adverse effect on our results of operations.
Corporate Information
Our principal executive offices are located at 2408 Timberloch Place, Suite B-7, The
Woodlands, Texas 77380 and our telephone number is (281) 719-3400. Our website address is
www.reprosrx.com. The information contained in our website is not a part of this prospectus
supplement or the accompanying prospectus.
Registered Direct Offering
On October 2, 2008, we completed a direct registered offering of 2.4 million shares of our
common stock at a purchase price of $6.50 per share for aggregate proceeds after expenses of
approximately $15.5 million. Certain of the purchasers under this offering were granted in their
purchase agreements an option to purchase an aggregate of up to $10 million of additional shares of
our common stock at the greater of the fair market value, defined as the average of the closing
prices for the 30 trading days immediately prior to the date of exercise, or $7.80 per share. Such
option becomes exercisable at such time as we have less than $10 million in cash and cash
equivalents and expires on September 29, 2009. In addition, the purchasers who received such
option also received a right of first offer to purchase their respective pro-rata portion of any
future financings, excluding certain corporate activities, that expires on September 29, 2010.
As part of the terms of the October 2, 2008 financing, we amended our Standstill Agreement
with Efficacy Capital Ltd. to permit Efficacy Capital to own up to 40% of our outstanding shares of
stock and to permit Efficacy Capital to designate two directors to serve on our Board of Directors.
Pursuant to that amendment, the Board increased its number to nine and appointed Mark Lappe, a
Managing Partner of Efficacy Capital, and John C. Reed, M.D., Ph.D., President and CEO of Burnham
Institute for Medical Research, to the vacancies on the Board created by such increase. The
Company amended its Rights Agreement to reflect the increase to 40% described above.
The shares of common stock offered by us in the offering were registered under our existing
shelf registration statement on Form S-3 (File No. 333-137109), which was filed with the Securities
and Exchange Commission on September 5, 2006 and declared effective by the Securities and Exchange
Commission on September 15, 2006.
In addition, the option described above also included our agreement to file a registration
statement with the Securities and Exchange Commission to register the resale of the shares issuable
upon exercise of such option and to have such registration statement declared effective by the
Securities and Exchange Commission as soon thereafter as possible. The registration statement
containing this prospectus is being filed pursuant to this option.
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RISK FACTORS
Investment in our securities involves a high degree of risk. You should consider carefully the
risk factors in any prospectus supplement and in our Annual Report on Form 10-K for the fiscal year
ended December 31, 2007, updates in Part II, Item 1A of our Form 10-Q filings, and in our future
filings with the Securities and Exchange Commission, as well as other information in this
prospectus and any prospectus supplement and the documents incorporated by reference herein or
therein, before purchasing any of our securities. Each of the risk factors could adversely affect
our business, operating results and financial condition, as well as adversely affect the value of
an investment in our securities.
FORWARD-LOOKING INFORMATION
Some of the statements contained (i) in this prospectus and any accompanying prospectus
supplement or (ii) incorporated by reference into this prospectus are 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 Securities Exchange Act of 1934, as amended, or the Exchange Act, and are
subject to the safe harbor created by the Securities Litigation Reform Act of 1995. Examples of
these forward-looking statements include, but are not limited to:
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our anticipated future capital requirements and the terms of any capital financing agreements; |
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timing and amount of future contractual payments, product revenue and operating expenses; |
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progress and results of clinical trials; |
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anticipated regulatory filings, requirements and future clinical trials; |
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protection of our intellectual property; and |
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market acceptance of our products and the estimated potential size of these markets. |
While these forward-looking statements made by us are based on our current intent, beliefs and
judgments, they are subject to risks and uncertainties that could cause actual results to vary from
the projections in the forward-looking statements. You should consider the risks below carefully in
addition to other information contained in this report before engaging in any transaction involving
shares of our common stock. If any of these risks occur, they could seriously harm our business,
financial condition or results of operations. In such case, the trading price of our common stock
could decline, and you may lose all or part of your investment.
The discussion and analysis set forth in this document contains discussions of regulatory
status and other forward-looking statements. Actual results could differ materially from those
projected in the forward-looking statement as a result of the following factors, among others:
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future capital requirements and additional fundings through equity or debt financings; |
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uncertainty of governmental regulatory requirements and lengthy approval process; |
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inability to fulfill our obligations under our license with the National Institutes of Health, or NIH, for Proellex may
result in forfeiture of our rights to Proellex; |
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results of the current Phase 2b trial for Androxal and the ongoing Phase 2 and 3 trials for Proellex; |
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history of operating losses and uncertainty of future financial results; |
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dependence on third parties for clinical development and manufacturing; |
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dependence on a limited number of key employees; |
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competition and risk of competitive new products; |
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ability to obtain and defend patents, protect trade secrets and avoid infringing patents held by third parties; |
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limitations on third-party reimbursement for medical and pharmaceutical products; |
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acceptance of our products by the medical community; |
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potential for product liability issues and related litigation; |
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potential for claims arising from the use of hazardous materials in our business; |
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continued listing on the Nasdaq Global Market; |
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volatility in the value of our common stock; |
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volatility in the financial markets generally; and |
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other factors set forth under Risk Factors contained in our Annual Report on Form 10-K for the fiscal year ended
December 31, 2007 filed with the Securities and Exchange Commission on March 17, 2008, updates in Part II, Item 1A of
our Form 10-Q filings, and in our future filings made with the Securities and Exchange Commission, which are
incorporated by reference in this prospectus, and any risk factors set forth in the accompanying prospectus supplement. |
In addition, in this prospectus, any prospectus supplement and the documents incorporated by
reference into this prospectus, the words believe, should, predict, future, may, will,
estimate, continue, anticipate, intend, plan, expect, potential, continue, or
opportunity, or other words and terms of similar meaning, as they relate to us, our business,
future financial or operating performance or our management, are intended to identify
forward-looking statements. Any forward-looking statement speaks only as of the date on which it is
made, and we undertake no obligation to update or revise any forward-looking statement to reflect
events or circumstances after the date on which the 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. Past financial or
operating performance is not necessarily a reliable indicator of future performance and you should
not use our historical performance to anticipate results or future period trends.
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USE OF PROCEEDS
Unless the applicable prospectus supplement states otherwise, the net proceeds we receive from
the sale of the securities offered by us under this prospectus will be used for general corporate
purposes, which may include:
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funding clinical trials and regulatory submissions for our two
lead product candidates, Proellex and Androxal, currently in human
clinical trials; |
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financing potential acquisitions of complementary businesses,
assets, technologies and products that we may consider from time
to time; and |
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general working capital. |
Although we currently have no plans to acquire any complementary businesses, our management
has broad discretion as to the allocation of the net proceeds received in this offering and may use
these proceeds for that purpose in the future. Pending these uses, we may temporarily use the net
proceeds to make short-term investments.
We will not receive any of the proceeds from the sale of the shares by the selling
stockholders.
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SELLING STOCKHOLDERS
On October 2, 2008 we sold 2,400,000 shares of our common stock in a direct registered
offering to certain investors. We provided rights to certain of such investors, the selling
stockholders under this prospectus, to purchase up to an aggregate of 1,282,052 shares of our
common stock at a purchase price equal to the fair market value at the time of exercise of such
purchase right or $7.80 per share, whichever is greater. In addition to the 5,000,000 shares to be
available for future offerings, this prospectus relates to the resale from time to time of up to a
total of 1,282,052 shares of common stock by the selling stockholders.
Pursuant to the terms of the purchase agreements relating to such purchase option rights, we
filed a Registration Statement on Form S-3, of which this prospectus constitutes a part, in order
to permit the selling stockholders, including their transferees who are affiliates, pledgees,
assignees and successors-in-interest, to resell to the public any or all of the shares of our
common stock issuable upon exercise of such purchase option rights, or any interests therein. When
we refer to the selling stockholders in this prospectus, we mean the entities listed in the table
below, as well as their transferees, pledgees or donees or its respective successors.
The following table, to our knowledge, sets forth information regarding the beneficial
ownership of our common stock by the selling stockholders as of October 31, 2008 and the number of
shares being offered hereby by the selling stockholders. The information is based in part on
information provided by or on behalf of the selling stockholders. Beneficial ownership is
determined in accordance with Rule 13d-3 promulgated by the SEC under the Securities Exchange Act
of 1934, as amended, or the Exchange Act, and includes voting or investment power with respect to
shares, as well as any shares as to which the selling stockholders have the right to acquire
beneficial ownership within sixty (60) days after October 31, 2008 through the exercise or
conversion of any stock options, warrants, convertible debt or otherwise. Unless otherwise
indicated below, the selling stockholders have sole voting and investment power with respect to
their shares of common stock. The inclusion of any shares in this table does not constitute an
admission of beneficial ownership by the selling stockholders. We will not receive any of the
proceeds from the sale of our common stock by the selling stockholders.
The actual number of shares of common stock that may be sold by the selling stockholders will
be determined by the selling stockholders. Because the selling stockholders may sell all, some or
none of the shares of common stock which they hold, no estimate can be given as to the number of
shares of common stock that will be held by the selling stockholders after completion of the sales.
The information set forth in the following table regarding the beneficial ownership after resale of
shares is based on the assumption that the selling stockholders will sell all of their shares of
common stock covered by this prospectus.
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Shares Beneficially |
|
|
|
|
|
Shares Beneficially |
|
|
Owned Before Offering(1) |
|
Shares Offered |
|
Owned After Offering(1) |
Name of Selling Stockholder |
|
Number |
|
Percent |
|
Hereby(2) |
|
Number |
|
Percent |
Efficacy Capital, Ltd.(3) |
|
|
4,292,136 |
|
|
|
28.28 |
% |
|
|
961,539 |
|
|
|
4,292,136 |
|
|
|
26.60 |
% |
Cyan Opportunities Fund, Ltd.(4) |
|
|
1,514,690 |
|
|
|
9.98 |
% |
|
|
294,872 |
|
|
|
1,514,690 |
|
|
|
9.79 |
% |
WR Multi Strategy Master Fund,
Ltd.(4) |
|
|
397,110 |
|
|
|
2.62 |
% |
|
|
25,641 |
|
|
|
397,110 |
|
|
|
2.61 |
% |
|
|
|
(1) |
|
The percentage of shares beneficially owned prior to the offering is based on 15,174,904
shares of our common stock issued and outstanding as of October 31, 2008 and the percentage of
shares beneficially owned after the offering is based on the same number of shares and assumes the
issuance of the shares offered by each particular selling stockholder.. |
|
(2) |
|
The shares listed in this column reflect the shares of common stock issuable upon exercise
of the purchase rights described above. Such purchase rights are not currently exercisable and are
thus not currently beneficially owned by the selling stockholders; therefore, the shares listed in
this column are not reflected in the columns reflecting beneficial ownership before the offering. |
|
(3) |
|
Efficacy Capital, Ltd., a Bermuda limited liability company, is the investment manager
for, and shares the power to vote and dispose of all of the securities listed above with, the
following entities: Efficacy Biotech Fund, L.P., a Delaware limited partnership, Efficacy Biotech
Fund Limited, a Bermuda Exempted Mutual Fund Company and Efficacy Biotech Master Fund Ltd., a
Bermuda Exempted Mutual Fund Company. Mark Lappe and Jon Faiz Kayyem, natural persons, have the
power to vote and dispose of all of the securities listed above as managing partners of Efficacy
Capital, LTD. Mark Lappe also serves on our board of directors. |
|
(4) |
|
Vermillion Asset Management LLC is the investment advisor to
a managed account for the WR Multi
Strategy Master Fund, Ltd. and is the investment manager of the Cyan Opportunities Fund, Ltd. |
7
PLAN OF DISTRIBUTION
We or the selling stockholders may sell the common stock through underwriters or dealers,
through agents, or directly to one or more purchasers. One or more prospectus supplements will
describe the terms of the offering of the common stock, including:
§ |
|
the name or names of any agents or underwriters; |
|
§ |
|
the purchase price of the common stock and the proceeds we will receive from the sale; |
|
§ |
|
any over-allotment options under which underwriters may purchase additional shares of common stock from us; |
|
§ |
|
any agency fees or underwriting discounts and other items constituting agents or underwriters compensation; |
|
§ |
|
any discounts or concessions allowed or reallowed or paid to dealers; and |
|
§ |
|
any securities exchange or market on which the common stock may be listed. |
Only underwriters named in the prospectus supplement are underwriters of the common stock
offered by the prospectus supplement.
If underwriters are used in the sale, they will acquire the common stock for their own account
and may resell the common stock 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.
The obligations of the underwriters to purchase the common stock will be subject to the conditions
set forth in the applicable underwriting agreement. We may offer the common stock to the public
through underwriting syndicates represented by managing underwriters or by underwriters without a
syndicate. Subject to certain conditions, the underwriters will be obligated to purchase all the
common stock offered by the prospectus supplement if they are to purchase any of such offered
shares. Any public offering price and any discounts or concessions allowed or reallowed or paid to
dealers may change from time to time. We may use underwriters with whom we have a material
relationship. We will describe in the prospectus supplement naming the underwriter, the nature of
any such relationship.
We or the selling stockholders may sell the common stock directly or through agents we
designate from time to time. We will name any agent involved in the offering and sale of the common
stock and we will describe any commissions we will pay the agent in the prospectus supplement.
We or the selling stockholders may authorize agents or underwriters to solicit offers by
certain types of institutional investors to purchase the common stock 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. We will describe the
conditions to these contracts and the commissions we must pay for solicitation of these contracts
in the prospectus supplement.
We may provide agents and underwriters with indemnification against certain civil liabilities,
including liabilities under the Securities Act, or contribution with respect to payments that the
agents or underwriters may make with respect to such liabilities. Agents and underwriters may
engage in transactions with, or perform services for, us in the ordinary course of business.
Any underwriter may engage in overallotment, stabilizing transactions, short covering
transactions and penalty bids in accordance with Regulation M under the Securities Exchange Act of
1934. Overallotment involves sales in excess of the offering size, which create a short position.
Stabilizing transactions permit bids to purchase the underlying shares of common stock so long as
the stabilizing bids do not exceed a specified maximum price. Short covering transactions involve
exercise by underwriters of an over-allotment option or purchases of the common stock in the open
market after the distribution is completed to cover short positions. Penalty bids permit the
underwriters to reclaim a selling concession from a dealer when the shares of common stock
originally sold by the dealer are purchased in a short covering transaction. Those activities may
cause the price of the common stock to be higher than it would otherwise be. If commenced, the
underwriters may discontinue any of the activities at any time.
Our common stock is quoted on the Nasdaq Global Market. One or more underwriters may make a
market in our common stock, but the underwriters will not be obligated to do so and may discontinue
market making at any time without notice. We cannot give any assurance as to liquidity of the
trading market for our common stock.
8
Any underwriters who are qualified market makers on the Nasdaq Global Market may engage in
passive market making transactions in the securities on the Nasdaq Global Market in accordance with
Rule 103 of Regulation M under the Securities Exchange Act of 1934, during the business day prior
to the pricing of the offering, before the commencement of offers or sales of the securities.
Passive market makers must comply with applicable volume and price limitations and must be
identified as passive market makers. In general, a passive market maker must display its bid at a
price not in excess of the highest independent bid for such security; if all independent bids are
lowered below the passive market makers bid, however, the passive market makers bid must then be
lowered when certain purchase limits are exceeded.
9
LEGAL MATTERS
The validity of the securities being offered hereby will be passed upon by Winstead PC, The
Woodlands, Texas. Jeffrey R. Harder, a member of the law firm Winstead PC, and a director of
Repros, beneficially owned as of October 31, 2008, an aggregate of 13,424 shares of our common
stock. Mr. Harder also holds options to purchase 55,000 shares of our common stock.
EXPERTS
The consolidated financial statements and managements assessment of the effectiveness of
internal control over financial reporting (which is included in Managements Report on Internal
Control over Financial Reporting) incorporated in this prospectus by reference to the Annual Report
on Form 10-K for the year ended December 31, 2007 have been so incorporated in reliance on the
report (which contains an explanatory paragraph relating to the Companys ability to continue as a
going concern as described in Note 2 to the consolidated financial statements) of
PricewaterhouseCoopers LLP, an independent registered public accounting firm, given on the
authority of said firm as experts in auditing and accounting.
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. We have filed with the
Securities and Exchange Commission a registration statement on Form S-3 under the Securities Act
with respect to the common stock we are offering under this prospectus. This prospectus does not
contain all of the information set forth in the registration statement and the exhibits to the
registration statement. For further information with respect to us and the common stock we are
offering under this prospectus, we refer you to the registration statement and the exhibits filed
as a part of the registration statement. You may read and copy the registration statement, as well
as our reports, proxy statements and other information, at the Securities and Exchange Commissions
public reference room at 100 F Street, N.E., Room 1580, Washington, D.C. 20549. You can request
copies of these documents by writing to the Securities and Exchange Commission and paying a fee for
the copying cost. Please call the Securities and Exchange Commission at 1-800-SEC-0330 for more
information about the operation of the public reference room. Our Securities and Exchange
Commission filings are also available at the Securities and Exchange Commissions website at
http://www.sec.gov.
The Securities and Exchange Commission allows us to incorporate by reference information
that we file with it, which means that we can disclose important information to you by referring
you to those documents. The information incorporated by reference is an important part of this
prospectus. Information in this prospectus supersedes information incorporated by reference that we
filed with the Securities and Exchange Commission prior to the date of this prospectus, while
information that we file later with the Securities and Exchange Commission will automatically
update and supersede this information. We incorporate by reference into this registration statement
and prospectus the documents listed below and any future filings we will make with the Securities
and Exchange Commission under Sections 13(a), 13(c), 14 or 15(d) of the Securities Exchange Act of
1934, as amended, after the date of the initial registration statement but prior to effectiveness
of the registration statement and after the date of this prospectus but prior to the termination of
the offering of the securities covered by this prospectus, except in each case for information
contained in any such filing where we indicate that such information is being furnished and is not
to be considered filed under the Securities Exchange Act of 1934, as amended.
The following documents filed with the Securities and Exchange Commission are incorporated by
reference in this prospectus:
§ |
|
our Annual Report on Form 10-K for the year ended December 31,
2007 filed with the Securities and Exchange Commission on
March 17, 2008; |
|
§ |
|
our Quarterly Reports on Form 10-Q for the quarters ended
March 31, 2008, June 30, 2008 and September 30, 2008 filed with
the Securities and Exchange Commission on May 12, August 11 and
November 10, 2008, respectively; |
|
§ |
|
our Current Reports on Form 8-K (other than information furnished
rather than filed), filed with the Securities and Exchange
Commission on January 8, 2008, January 10, 2008, February 1, 2008,
February 11, 2008, February 12, 2008, February 22, 2008, March 7,
2008, March 14, 2008, March 18, 2008, March 31, 2008, April 4,
2008, May 8, 2008, May 12, 2008, May 28, 2008, May 29, 2008, June
10, 2008, June 30, 2008, July 11, 2008, July 15, 2008, July 21,
2008, July 28, 2008, August 11, 2008, August 18, 2008, August 21,
2008, September 29, 2008, October 2, 2008, October 10, 2008,
October 29, 2008, November 10, 2008 and November 12, 2008; and |
10
§ |
|
the description of our common stock contained in our registration
statement on Form 8-A filed with the Securities and Exchange
Commission on February 2, 1993, including all amendments and
reports filed for the purpose of updating such information. |
Information furnished to the Securities and Exchange Commission under Item 2.02 or Item 7.01
in Current Reports on Form 8-K, and any exhibit relating to such information, filed prior to, on or
subsequent to the date of this prospectus is not incorporated by reference into this prospectus.
We will furnish without charge to you, upon written or oral request, a copy of any or all of
the documents incorporated by reference, including exhibits to these documents. You should direct
any requests for documents to Repros Therapeutics Inc., Attention: Secretary, 2408 Timberloch
Place, Suite B-7, The Woodlands, Texas 77380. Our telephone number is (281) 719-3400.
11
PART II
INFORMATION NOT REQUIRED IN THE PROSPECTUS
Item 14. Other Expenses of Issuance and Distribution
The following table sets forth the estimated costs and expenses, other than the underwriting
discounts and commissions, payable by the registrant in connection with the offering of the
securities being registered. All the amounts shown are estimates, except for the registration fee.
|
|
|
|
|
|
|
|
|
|
Securities and Exchange Commission registration fee |
|
$ |
5,000 |
|
NASD registration fee |
|
|
45,000 |
|
Accounting fees and expenses |
|
|
200,000 |
|
Legal fees and expenses |
|
|
150,000 |
|
Printing, transfer agent and miscellaneous expenses |
|
|
100,000 |
|
|
|
|
|
Total: |
|
$ |
500,000 |
|
|
|
|
|
Item 15. Indemnification of Officers and Directors
Section 145 of the Delaware General Corporation Law, or Delaware law, inter alia, empowers a
Delaware corporation to indemnify any person who was or is a party or is threatened to be made a
party to any threatened, pending or completed action, suit or proceeding (other than an action by
or in the right of the corporation) by reason of the fact that such person is or was a director,
officer, employee or agent of the corporation, or is or was serving at the request of the
corporation as a director, officer, employee or agent of another corporation or other enterprise,
against expenses (including attorneys fees), judgments, fines and amounts paid in settlement
actually and reasonably incurred by him in connection with such action, suit or proceeding if he
acted in good faith and in a manner he reasonably believed to be in or not opposed to the best
interests of the corporation, and, with respect to any criminal action or proceeding, had no
reasonable cause to believe his conduct was unlawful. Similar indemnity is authorized for such
persons against expenses (including attorneys fees) actually and reasonably incurred in connection
with the defense or settlement of any such threatened, pending or completed action or suit if such
person acted in good faith and in a manner he reasonably believed to be in or not opposed to the
best interests of the corporation, and provided further that (unless a court of competent
jurisdiction otherwise provides) such person shall not have been adjudged liable to the
corporation. Any such indemnification may be made only as authorized in each specific case upon a
determination by the stockholders or disinterested directors or by independent legal counsel in a
written opinion that indemnification is proper because the indemnitee has met the applicable
standard of conduct.
Section 145 further authorizes a corporation to purchase and maintain insurance on behalf of
any person who is or was a director, officer, employee or agent of the corporation, or is or was
serving at the request of the corporation as a director, officer, employee or agent of another
corporation or enterprise, against any liability asserted against him and incurred by him in any
such capacity, or arising out of his status as such, whether or not the corporation would otherwise
have the power to indemnify him under Section 145. We maintain policies insuring our officers and
directors against certain liabilities for actions taken in such capacities, including liabilities
under the Securities Act of 1933, as amended (the Securities Act).
Our Restated Certificate of Incorporation and Restated Bylaws require us to indemnify our
directors to the fullest extent permitted under Delaware law or any other applicable law in effect,
but if such statute or law is amended, we may change the standard of indemnification only to the
extent that such amended statute or law permits us to provide broader indemnification rights to our
directors. We must indemnify such officers and employees in the same manner and to the same extent
that we are required to indemnify our directors under our Restated Certificate of Incorporation and
Restated Bylaws. Our Restated Certificate of Incorporation limits the personal liability of a
director to us or our stockholders to damages for breach of the directors fiduciary duty.
The underwriting agreement that we might enter into (Exhibit 1.1) will provide for
indemnification by any underwriters of Repros, our directors, our officers who sign the
registration statement and our controlling persons for some liabilities, including liabilities
arising under the Securities Act of 1933.
II-1
Item 16. Exhibits and Financial Statement Schedules
(a) Exhibits
|
|
|
Exhibit Number |
|
Identification of Exhibit |
1.1
|
|
Form of Underwriting Agreement.(1) |
|
|
|
3.1(a)
|
|
Restated Certificate of Incorporation. Exhibit 3.3 to the Companys Registration
Statement on Form SB-2 (No. 33-57728-FW), as amended (Registration Statement), is
incorporated herein by reference. |
|
|
|
3.1(b)
|
|
Certificate of Amendment to Restated Certificate of Incorporation. Exhibit 3.1 to
the Companys Current Report on Form 8-K dated May 1, 2006 is incorporated herein by
reference. |
|
|
|
3.1(c)
|
|
Certificate of Designation of Series One Junior Participating Preferred Stock dated
September 2, 1999. Exhibit A to Exhibit 4.1 to the Companys Registration Statement
on Form 8-A as filed with the Commission on September 3, 1999 (the Rights Plan
Registration Statement), is incorporated herein by reference. |
|
|
|
3.2
|
|
Restated Bylaws of the Company. Exhibit 3.4 to the Registration Statement is
incorporated herein by reference. |
|
|
|
4.1
|
|
Specimen Common Stock Certificate, $.001 par value, of the Company. Exhibit 4.1 to
the Registration Statement is incorporated herein by reference. |
|
|
|
4.2
|
|
Rights Agreement dated September 1, 1999 between the Company and Computershare
Investor Services LLC (as successor in interest to Harris Trust & Savings Bank), as
Rights Agent. Exhibit 4.1 to the Rights Plan Registration Statement is incorporated
herein by reference. |
|
|
|
4.3
|
|
First Amendment to Rights Agreement, dated as of September 6, 2002, between the
Company, Harris Trust & Savings Bank and Computershare Investor Services LLC.
Exhibit 4.3 to Amendment No. 1 to the Rights Plan Registration Statement on Form
8-A/A as filed with the Commission on September 11, 2002 is incorporated herein by
reference. |
|
|
|
4.4
|
|
Second Amendment to Rights Agreement, dated as of October 30, 2002, between the
Company and Computershare Investor Services LLC. Exhibit 4.4 to Amendment No. 2 to
the Rights Plan Registration Statement on Form 8-A/A as filed with the Commission on
October 31, 2002 is incorporated herein by reference. |
|
|
|
4.5
|
|
Third Amendment to Rights Agreement, dated as of June 30, 2005, between the Company
and Computershare Trust Company, N.A. Exhibit 4.4 to the Companys Current Report on
Form 8-K as filed with the Commission on June 30, 2005 is incorporated herein by
reference. |
|
|
|
4.6
|
|
Fourth Amendment to Rights Agreement, dated as of January 9, 2008, between the
Company and Computershare Trust Company, N.A. Exhibit 4.5 to the Companys Current
Report on Form 8-K as filed with the Commission on January 10, 2008 is incorporated
herein by reference. |
|
|
|
4.7
|
|
Fifth Amendment to Rights Agreement, dated as of October 10, 2008, between the
Company and Computershare Trust Company, N.A. Exhibit 4.6 to the Companys Current
Report on Form 8-K as filed with the Commission on October 10, 2008 is incorporated
herein by reference. |
|
|
|
4.8
|
|
Form of Rights Certificate. Exhibit B to Exhibit 4.1 to the Rights Plan Registration
Statement is incorporated herein by reference. |
|
|
|
+5.1
|
|
Opinion of Winstead PC. |
|
|
|
23.1*
|
|
Consent of PricewaterhouseCoopers LLP, independent registered public accounting firm. |
|
|
|
+23.2
|
|
Consent of Winstead PC (included in Exhibit 5.1). |
|
|
|
+24.1
|
|
Power of Attorney (included in the signature page of this registration statement when initially filed). |
|
|
|
* |
|
Filed herewith. |
|
+ |
|
Previously filed. |
|
(1) |
|
To be filed by amendment or as an exhibit to a current report of the registrant on Form 8-K
and incorporated herein by reference as applicable. |
II-2
Item 17. Undertakings
The undersigned registrant hereby undertakes:
(1) To file, during any period in which offers or sales are being made, a post-effective
amendment to this registration statement:
(i) to include any prospectus required by section 10(a)(3) of the Securities Act of 1933;
(ii) to reflect in the prospectus any facts or events arising after the effective date of the
registration statement (or the most recent post-effective amendment thereof) which, individually or
in the aggregate, represent a fundamental change in the information set forth in the registration
statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered
(if the total dollar value of securities offered would not exceed that which was registered) and
any deviation from the low or high end of the estimated maximum offering range may be reflected in
the form of prospectus filed with the Securities and Exchange Commission pursuant to Rule 424(b)
if, in the aggregate, the changes in volume and price represent no more than a 20 percent change in
the maximum aggregate offering price set forth in the Calculation of Registration Fee table in
the effective registration statement; and
(iii) to include any material information with respect to the plan of distribution not
previously disclosed in the registration statement or any material change to such information in
the registration statement; provided, however, that paragraphs (1)(i), (1)(ii) and (1)(iii) do not
apply if the information required to be included in a post-effective amendment by those paragraphs
is contained in periodic reports filed with or furnished to the Securities and Exchange Commission
by the registrant pursuant to section 13 or 15(d) of the Securities Exchange Act of 1934 that are
incorporated by reference in the registration statement, or is contained in a form of prospectus
filed pursuant to Rule 424(b) that is part of the registration statement.
(2) That, for the purpose of determining any liability under the Securities Act of 1933, each
such post-effective amendment shall be deemed to be a new registration statement relating to the
securities offered therein, and the offering of the securities at that time shall be deemed to be
the initial bona fide offering thereof.
(3) To remove from registration by means of a post-effective amendment any of the securities
being registered which remain unsold at the termination of this offering.
(4) That, for the purpose of determining liability of a registrant under the Securities Act to
any purchaser in the initial distribution of the securities, the undersigned registrant undertakes
that in a primary offering of securities of the undersigned registrant pursuant to this
registration statement, regardless of the underwriting method used to sell the securities to the
purchaser, if the securities are offered or sold to such purchaser by means of any of the following
communications, the undersigned registrant will be a seller to the purchaser and will be considered
to offer or sell such securities to such purchaser:
(i) Any preliminary prospectus or prospectus of the undersigned registrant relating to the
offering required to be filed pursuant to Rule 424;
(ii) Any free writing prospectus relating to the offering prepared by or on behalf of the
undersigned registrant or used or referred to by the undersigned registrant;
(iii) The portion of any other free writing prospectus relating to the offering containing
material information about the undersigned registrant or its securities provided by or on behalf of
the undersigned registrant; and
(iv) Any other communication that is an offer in the offering made by the undersigned
registrant to the purchaser.
(5) That, for purposes of determining any liability under the Securities Act of 1933, each
filing of the registrants annual report pursuant to section 13(a) or section 15(d) of the
Securities Exchange Act of 1934 (and, where applicable, each filing of an employee benefit plans
annual report pursuant to section 15(d) of the Securities Exchange Act of 1934) that is
incorporated by reference in the registration statement shall be deemed to be a new registration
statement relating to the securities offered therein, and the offering of such securities at that
time shall be deemed to be the initial bona fide offering thereof.
(6) That: (i) for purposes of determining any liability under the Securities Act of 1933, the
information omitted from the form of prospectus filed as part of this registration statement in
reliance upon Rule 430A and contained in the form of
II-3
prospectus filed by the registrant pursuant to Rule 424(b)(1) or (4) or 497(h) under the
Securities Act of 1933 shall be deemed to be part of the registration statement as of the time it
was declared effective; and (ii) for the purpose of determining any liability under the Securities
Act of 1933, each post-effective amendment that contains a form of prospectus shall be deemed to be
a new registration statement relating to the securities offered therein, and the offering of such
securities at that time shall be deemed to be the initial bona fide offering thereof.
Insofar as indemnification for liabilities arising under the Securities Act of 1933 may be
permitted to directors, officers and controlling persons of the registrant pursuant to the
foregoing provisions, or otherwise, the registrant has been advised that in the opinion of the
Securities and Exchange Commission such indemnification is against public policy as expressed in
the Securities Act of 1933 and is, therefore, unenforceable. In the event that a claim for
indemnification against such liabilities (other than the payment by the registrant of expenses
incurred or paid by a director, officer or controlling person of the registrant in the successful
defense of any action, suit or proceeding) is asserted by a director, officer or controlling person
in connection with the securities being registered, the registrant will, unless in the opinion of
its counsel the matter has been settled by controlling precedent, submit to a court of appropriate
jurisdiction the question whether such indemnification by it is against public policy as expressed
in the Securities Act of 1933 and will be governed by the final adjudication of such issue.
II-4
SIGNATURES
Pursuant to the requirements of the Securities Act of 1933, the registrant certifies that it
has reasonable grounds to believe that it meets all of the requirements for filing on Form S-3 and
has duly caused this registration statement to be signed on its behalf by the undersigned,
thereunto duly authorized, in The Woodlands, Montgomery County, State of Texas, on November 20,
2008.
|
|
|
|
|
|
REPROS THERAPEUTICS INC.
|
|
|
By: |
/s/ Joseph S. Podolski
|
|
|
|
Joseph S. Podolski |
|
|
|
President and Chief Executive Officer |
|
|
II-5
Pursuant to the requirements of the Securities Act of 1933, this registration statement has
been signed below by the following persons in the capacities and on the dates indicated.
|
|
|
|
|
Signatures |
|
Title |
|
Date |
|
|
|
|
|
/s/ Joseph S. Podolski
Joseph S. Podolski
|
|
President, Chief Executive Officer
and Director
(Principal Executive Officer)
|
|
November 20, 2008 |
|
|
|
|
|
|
|
|
|
|
/s/ Louis Ploth, Jr.
Louis Ploth, Jr.
|
|
Vice President, Business Development,
Chief Financial Officer, Secretary
and Director (Principal Financial
and Accounting Officer)
|
|
November 20, 2008 |
|
|
|
|
|
|
|
|
|
|
|
|
Chairman of the Board
|
|
November 20, 2008 |
|
|
|
|
|
*
Jean L. Fourcroy, M.D., Ph.D., M.P.H.
|
|
Director
|
|
November 20, 2008 |
|
|
|
|
|
|
|
Director
|
|
November 20, 2008 |
|
|
|
|
|
|
|
Director
|
|
November 20, 2008 |
|
|
|
|
|
|
|
Director
|
|
November 20, 2008 |
|
|
|
|
|
|
|
Director
|
|
November 20, 2008 |
|
|
|
|
|
*
John C. Reed, M.D., Ph.D.
|
|
Director
|
|
November 20, 2008 |
|
|
|
|
|
Signatures |
|
Title |
|
Date |
|
/s/ Louis Ploth, Jr.
* By: Attorney-in-fact |
|
|
|
November 20, 2008 |
II-6
INDEX TO EXHIBITS
|
|
|
Exhibit Number |
|
Identification of Exhibit |
1.1
|
|
Form of Underwriting Agreement.(1) |
|
|
|
3.1(a)
|
|
Restated Certificate of Incorporation. Exhibit 3.3 to the Companys Registration
Statement on Form SB-2 (No. 33-57728-FW), as amended (Registration Statement), is
incorporated herein by reference. |
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3.1(b)
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Certificate of Amendment to Restated Certificate of Incorporation. Exhibit 3.1 to
the Companys Current Report on Form 8-K dated May 1, 2006 is incorporated herein by
reference. |
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3.1(c)
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Certificate of Designation of Series One Junior Participating Preferred Stock dated
September 2, 1999. Exhibit A to Exhibit 4.1 to the Companys Registration Statement
on Form 8-A as filed with the Commission on September 3, 1999 (the Rights Plan
Registration Statement), is incorporated herein by reference. |
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3.2
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Restated Bylaws of the Company. Exhibit 3.4 to the Registration Statement is
incorporated herein by reference. |
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4.1
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Specimen Common Stock Certificate, $.001 par value, of the Company. Exhibit 4.1 to
the Registration Statement is incorporated herein by reference. |
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4.2
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Rights Agreement dated September 1, 1999 between the Company and Computershare
Investor Services LLC (as successor in interest to Harris Trust & Savings Bank), as
Rights Agent. Exhibit 4.1 to the Rights Plan Registration Statement is incorporated
herein by reference. |
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4.3
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First Amendment to Rights Agreement, dated as of September 6, 2002, between the
Company, Harris Trust & Savings Bank and Computershare Investor Services LLC.
Exhibit 4.3 to Amendment No. 1 to the Rights Plan Registration Statement on Form
8-A/A as filed with the Commission on September 11, 2002 is incorporated herein by
reference. |
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4.4
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Second Amendment to Rights Agreement, dated as of October 30, 2002, between the
Company and Computershare Investor Services LLC. Exhibit 4.4 to Amendment No. 2 to
the Rights Plan Registration Statement on Form 8-A/A as filed with the Commission on
October 31, 2002 is incorporated herein by reference. |
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4.5
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Third Amendment to Rights Agreement, dated as of June 30, 2005, between the Company
and Computershare Trust Company, Inc. (as successor in interest to Computershare
Investor Services, LLC). Exhibit 4.4 to the Companys Current Report on Form 8-K as
filed with the Commission on June 30, 2005 is incorporated herein by reference. |
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4.6
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Fourth Amendment to Rights Agreement, dated as of January 9, 2008, between the
Company and Computershare Trust Company, Inc. (as successor in interest to
Computershare Investor Services, LLC). Exhibit 4.5 to the Companys Current Report
on Form 8-K as filed with the Commission on January 10, 2008 is incorporated herein
by reference. |
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4.7
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Fifth Amendment to Rights Agreement, dated as of October 10, 2008, between the
Company and Computershare Trust Company, N.A. Exhibit 4.6 to the Companys Current
Report on Form 8-K as filed with the Commission on October 10, 2008 is incorporated
herein by reference. |
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4.8
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Form of Rights Certificate. Exhibit B to Exhibit 4.1 to the Rights Plan Registration
Statement is incorporated herein by reference. |
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+5.1
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Opinion of Winstead PC. |
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23.1*
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Consent of PricewaterhouseCoopers LLP, independent registered public accounting firm. |
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+23.2
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Consent of Winstead PC (included in Exhibit 5.1). |
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+24.1
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Power of Attorney (included in the signature page of this registration statement when initially filed). |
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* |
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Filed herewith. |
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+ |
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Previously filed. |
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(1) |
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To be filed by amendment or as an exhibit to a current report of the registrant on Form 8-K
and incorporated herein by reference, as applicable. |
II-7