424B5
Filed pursuant to Rule 424(b)(5)
Registration Statement
No. 333-121225
PROSPECTUS SUPPLEMENT
(To Prospectus dated February 10,
2005)
7,600,000 Shares
Regeneron Pharmaceuticals,
Inc.
COMMON STOCK
We are selling 7,600,000 shares of
our common stock to Morgan Stanley & Co. Incorporated.
Our common stock is listed on the Nasdaq
Global Market under the symbol REGN. The last
reported sale price of shares of our common stock as reported on
the Nasdaq Global Market on November 13, 2006 was $24.28.
Investing in our common stock
involves a high degree of risk. See Risk Factors
beginning on page 43 of our Quarterly Report on
Form 10-Q for the
quarter ended September 30, 2006, which is incorporated
herein by reference, to read about risks that you should
consider before buying shares of our common stock.
Morgan Stanley & Co. Incorporated
has agreed to purchase the 7,600,000 shares of common stock
from us at a price of $23.03 per share which will result in
$175,028,000 of proceeds to us before expenses.
Morgan Stanley & Co. Incorporated
proposes to offer the common stock in transactions on the NASDAQ
Global Market, in the
over-the-counter market
or through negotiated transactions at market prices or
negotiated prices.
Neither the Securities and Exchange
Commission nor any state securities commission has approved or
disapproved these securities or determined if this prospectus
supplement or the prospectus to which it relates is truthful or
complete. Any representation to the contrary is a criminal
offense.
MORGAN STANLEY
November 13, 2006
TABLE OF CONTENTS
Prospectus Supplement
|
|
|
|
|
|
|
Page | |
|
|
| |
|
|
|
S-1 |
|
|
|
|
S-2 |
|
|
|
|
S-3 |
|
|
|
|
S-4 |
|
|
|
|
S-5 |
|
|
|
|
S-8 |
|
Where You Can Find More Information
|
|
|
S-8 |
|
Prospectus
|
|
|
|
|
|
|
|
|
Page |
|
|
|
|
|
|
|
|
i |
|
|
|
|
i |
|
|
|
|
ii |
|
|
|
|
1 |
|
|
|
|
2 |
|
|
|
|
13 |
|
|
|
|
13 |
|
|
|
|
13 |
|
|
|
|
|
13 |
|
|
|
|
|
17 |
|
|
|
|
|
26 |
|
|
|
|
28 |
|
|
|
|
29 |
|
|
|
|
29 |
|
You should rely only on the information
incorporated by reference or provided in this prospectus
supplement and the accompanying prospectus. Neither we nor the
underwriter have authorized anyone to provide you with
additional or different information. If anyone provided you with
additional or different information, you should not rely on it.
Neither we nor the underwriter are making an offer to sell these
securities in any jurisdiction where the offer or sale is not
permitted. You should assume that the information contained in
this prospectus supplement, the accompanying prospectus and the
documents incorporated by reference is accurate only as of their
respective dates. Our business, financial condition, results of
operations and prospects may have changed since those dates.
i
PROSPECTUS SUPPLEMENT SUMMARY
This summary highlights information
contained elsewhere in this prospectus supplement and the
accompanying prospectus. It does not contain all the information
that you may consider important in making your investment
decision. Therefore, you should read the entire prospectus
supplement and the accompanying prospectus and the information
incorporated by reference herein and therein carefully,
including in particular the Risk Factors sections
and the financial statements and related notes incorporated by
reference in this prospectus supplement. Unless the context
otherwise requires, the terms we, our,
us, the Company and
Regeneron refer to Regeneron Pharmaceuticals,
Inc.
Overview
Regeneron Pharmaceuticals, Inc. is a
biopharmaceutical company that discovers, develops, and intends
to commercialize pharmaceutical products for the treatment of
serious medical conditions. We are currently focused on three
development programs: VEGF Trap in oncology, VEGF Trap eye
formulation (VEGF Trap-Eye) in eye diseases using intraocular
delivery, and the IL-1
Trap (rilonacept) in various inflammatory indications. The
VEGF Trap is being developed in oncology in collaboration with
the sanofi-aventis Group. In October 2006, we entered into a
collaboration with Bayer HealthCare LLC for the development of
the VEGF Trap-Eye. Our preclinical research programs are in the
areas of oncology and angiogenesis, ophthalmology, metabolic and
related diseases, muscle diseases and disorders, inflammation
and immune diseases, bone and cartilage, pain, and
cardiovascular diseases. We expect that our next generation of
product candidates will be based on our proprietary technologies
for developing human monoclonal antibodies. Developing and
commercializing new medicines entails significant risk and
expense. Since inception we have not generated any sales or
profits from the commercialization of any of our product
candidates.
Our core business strategy is to maintain
a strong foundation in basic scientific research and
discovery-enabling technology and combine that foundation with
our manufacturing and clinical development capabilities to build
a successful, integrated biopharmaceutical company. Our efforts
have yielded a diverse pipeline of product candidates that we
believe has the potential to address a variety of serious
medical conditions. We believe that our ability to develop
product candidates is enhanced by the application of our
technology platforms. Our discovery platforms are designed to
identify specific genes of therapeutic interest for a particular
disease or cell type and validate targets through
high-throughput production of mammalian models. Our human
monoclonal antibody
(VelocImmune®)
and cell line expression technologies may then be utilized to
design and produce new product candidates directed against the
disease target. Based on the strength of the VelocImmune
platform, which we believe, in conjunction with our other
proprietary technologies, can accelerate the development of
fully human monoclonal antibodies, we plan to move two new
antibody candidates into clinical trials each year going forward
beginning in 2007. We continue to invest in the development of
enabling technologies to assist in our efforts to identify,
develop, and commercialize new product candidates.
We were incorporated as a New York
corporation on January 8, 1988. Our common stock is listed
on the Nasdaq Global Market under the symbol REGN.
Our headquarters and principal executive offices are located at
777 Old Saw Mill River Road, Tarrytown, New York
10591-6707. Our
telephone number is
(914) 347-7000.
You can get more information regarding our
business by reading our Annual Report on
Form 10-K for the
fiscal year ended December 31, 2005, and the other reports
we file with the SEC. See Where You Can Find More
Information on
page S-8 of this
prospectus supplement.
S-1
THE OFFERING
|
|
|
Common stock offered |
|
7,600,000 shares of our common stock.
|
|
Shares outstanding after the offering:
|
|
|
|
Common stock
|
|
62,735,904
|
|
Class A
stock
|
|
2,296,928
|
|
Total
|
|
65,032,832
|
|
Use of Proceeds
|
|
We currently intend to use the net
proceeds of this offering to fund pre-clinical and clinical
development of our product candidates, to fund basic research
activities, to continue development of our technology platforms,
for capital expenditures, to redeem, repay or purchase our
51/2% convertible
senior subordinated notes due October 17, 2008, and for
general corporate purposes, including working capital,
acquisitions and other business opportunities. See Use of
Proceeds.
|
|
Nasdaq Global Market symbol
|
|
REGN
|
|
Risk Factors
|
|
Before investing in our common stock, you
should carefully read and consider the information set forth in
Risk Factors beginning on page 43 of our
Quarterly Report on
Form 10-Q for the
quarter ended September 30, 2006, which is incorporated
herein by reference. |
The number of shares of common stock to be
outstanding after the offering is based on the number of shares
of common stock outstanding as of October 31, 2006 and
excludes as of that date an aggregate of 13,688,889 shares
of our common stock subject to options outstanding as of that
date under our 1990 and 2000 Long-Term Incentive Plans, of which
6,722,416 were exercisable as of that date.
S-2
USE OF PROCEEDS
We will receive approximately
$175 million of proceeds before expenses from the sale of
7,600,000 shares of our common stock. We currently intend
to use the net proceeds of this offering to fund pre-clinical
and clinical development of our product candidates, to fund
basic research activities, to continue development of our
technology platforms, for capital expenditures, to redeem, repay
or purchase our
51/2% convertible
senior subordinated notes due October 17, 2008, and for
general corporate purposes, including working capital,
acquisitions, and other business opportunities.
S-3
DILUTION
As of September 30, 2006, our net
tangible book value before the offering was $62.5 million
or $1.09 per common share. Net tangible book value
per share is determined by dividing our net tangible book
value (total assets less total liabilities) by the number of
common shares outstanding. After giving effect to the sale of
the shares of our common stock in this offering at a price of
$23.03 per share and after deducting the estimated expenses
of this offering, our pro forma net tangible book value as of
September 30, 2006 would have been $236.6 million in
the aggregate, or $3.66 per common share. This represents
an immediate increase in net tangible book value of
$2.57 per common share to existing holders and immediate
dilution of $19.37 per common share to new investors
purchasing shares of common stock in this offering. The
following table illustrates this per share dilution:
|
|
|
|
|
|
|
|
|
|
Assumed public offering price
|
|
|
|
|
|
$ |
23.03 |
|
|
Net tangible book value per common share before this offering
|
|
$ |
1.09 |
|
|
|
|
|
|
Increase attributable to new investors
|
|
|
2.57 |
|
|
|
|
|
|
|
|
|
|
|
|
Pro forma net tangible book value per common share after this
offering
|
|
|
|
|
|
|
3.66 |
|
|
|
|
|
|
|
|
Dilution per common share to new investors
|
|
|
|
|
|
$ |
19.37 |
|
|
|
|
|
|
|
|
Dilution per common share to new
investors means the difference between the price per share
of common stock of $23.03 and the pro forma net tangible book
value per common share after giving effect to the sale to the
underwriter of the shares offered hereby.
The foregoing table does not take into
effect further dilution to new investors that could occur upon
the exercise of outstanding options having a per share exercise
price less than the offering price per share in this offering.
As of October 31, 2006 there were an aggregate of
13,688,889 shares of our common stock subject to options
outstanding as of that date under our 1990 and 2000 Long-Term
Incentive Plans, of which 6,722,416 were exercisable as of that
date.
S-4
PLAN OF DISTRIBUTION
We and Morgan Stanley & Co.
Incorporated have entered into an underwriting agreement with
respect to the 7,600,000 shares of Common Stock being
offered hereby.
The underwriter has agreed to purchase the
common stock from us at a price of $23.03 per share, which
will result in approximately $175 million of proceeds in
the aggregate to us before expenses.
The underwriter proposes to offer the
shares of common stock from time to time for sale in one or more
transactions on the NASDAQ Global Market, in the
over-the-counter
market, through negotiated transactions or otherwise at market
prices prevailing at the time of sale, at prices related to
prevailing market prices or at negotiated prices, subject to
receipt and acceptance by it and subject to its right to reject
any order in whole or in part. In connection with the sale of
the shares of common stock offered hereby, the underwriter may
be deemed to have received compensation in the form of
underwriting discounts. The underwriter may receive from
purchasers of the shares normal brokerage commissions in amounts
agreed with such purchasers. In addition, the underwriter may
receive a commission from certain investors equivalent to five
cents per share. The underwriter may effect such transactions by
selling shares of common stock to or through dealers, and such
dealers may receive compensation in the form of discounts,
concessions or commissions from the underwriter or purchasers of
shares of common stock for whom they may act as agents or to
whom they may sell as principal.
In connection with the offering, the
underwriter may purchase and sell shares of common stock in the
open market. These transactions may include short sales and
purchases to cover positions created by short sales. Short sales
involve the sale by an underwriter of a greater number of shares
than it is required to purchase in the offering. The underwriter
will need to close out any short sale by purchasing shares in
the open market. The underwriter is likely to create a short
position if it is concerned that there may be downward pressure
on the price of the common stock in the open market after
pricing that could adversely affect investors who purchase in
the offering. Purchases to cover a short position, as well as
other purchases by the underwriter for its own account, may have
the effect of preventing or retarding a decline in the market
price of the companys stock, and may maintain or otherwise
affect the market price of the common stock. As a result, the
price of the common stock may be higher than the price that
otherwise might exist in the open market. If these activities
are commenced, they may be discontinued at any time. These
transactions may be effected on NASDAQ Global Market, in the
over-the-counter market
or otherwise.
Our common stock is listed on the NASDAQ
Global Market under the symbol REGN.
We estimate that our total expenses of
this offering will be approximately $950,000.
Each of us, our directors and our
executive officers has agreed that, with the exception of the
common stock being offered pursuant to this prospectus
supplement and without the prior written consent of Morgan
Stanley & Co. Incorporated, each of us, our directors
and our executive officers will not, during the period ending
90 days after the date of this prospectus supplement:
|
|
|
|
|
offer, pledge, sell, contract to sell,
sell any option or contract to purchase, purchase any option or
contract to sell, grant any option, right or warrant to
purchase, lend or otherwise transfer or dispose of directly or
indirectly, any shares of our common stock or any securities
convertible into or exercisable or exchangeable for our common
stock; or
|
|
|
|
enter into any swap or other arrangement
that transfers to another, in whole or in part, any of the
economic consequences of ownership of the common stock,
|
whether any transaction described above is
to be settled by delivery of common stock or such other
securities, in cash or otherwise.
The restrictions described in the
preceding paragraph do not apply to:
|
|
|
|
|
the sale of shares to the underwriter;
|
|
|
|
the issuance by us of shares of common
stock upon the exercise of an option or a warrant or the
conversion of a security outstanding on the date of this
prospectus of which the underwriter has been
|
S-5
|
|
|
|
|
advised in writing or which is described
in this prospectus supplement and the accompanying prospectus;
|
|
|
|
the grant of options or the issuance of
shares of common stock by us to employees, officers, directors,
advisors or consultants pursuant to any employee benefit plan
described in this prospectus supplement and the accompanying
prospectus;
|
|
|
|
the issuance of any shares of common stock
by us in connection with an acquisition, licensing,
collaboration or similar strategic arrangements, provided that
the recipient of any such shares also agrees to the restrictions
described above;
|
|
|
|
the issuance by us of shares of common
stock as matching contributions under our 401(k) plan;
|
|
|
|
transactions by any person other than us
relating to shares of common stock or other securities acquired
in open market transactions after the completion of the offering
of the shares;
|
|
|
|
transfers by any person other than us that
are bona fide gifts;
|
|
|
|
certain distributions or transfers by any
person other than us to family member, trusts and/or controlled
entities of such person in connection with estate planning,
provided that each transferee also agrees to the restrictions
described above;
|
|
|
|
transactions in connection with a trading
plan pursuant to
Rule 10b5-1 under
the Exchange Act of 1934, provided that such trading plan was in
existence prior to the date of this prospectus
supplement; or |
|
|
|
the sale of shares of common stock by our
directors and executive officers as to which written permission
is provided by us, provided that the aggregate number of shares
sold in reliance on this clause shall not exceed
250,000 shares.
|
The underwriter has represented and agreed
that:
(a) it has only communicated or
caused to be communicated and will only communicate or cause to
be communicated an invitation or inducement to engage in
investment activity (within the meaning of Section 21 of
the Financial Services and Markets Act 2000 (the
FSMA) to persons who are investment professionals
falling within Article 19(5) of the Financial Services and
Markets Act 2000 (Financial Promotion) Order 2005 or in
circumstances in which Section 21(1) of the FSMA does not
apply to us; and
(b) it has complied and will comply
with all applicable provisions of the FSMA with respect to
anything done by it in relation to the shares in, from or
otherwise involving the United Kingdom.
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 shares which are the subject of this
offering contemplated by this prospectus supplement 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:
(a) to legal entities which are
authorized or regulated to operate in the financial markets or,
if not so authorized or regulated, whose corporate purpose is
solely to invest in securities;
(b) 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; or
(c) 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 underwriter; or
S-6
(d) in any other circumstances
falling within Article 3 (2) of the Prospectus
Directive, provided that no such offer of shares shall result in
a requirement for the publication by us or any underwriter of a
prospectus pursuant to Article 3 of the Prospectus
Directive.
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 the shares to be offered so as to enable an
investor to decide to purchase or subscribe the shares, as the
same may be varied in that Member State by any measure
implementing the Prospectus Directive in that Member State and
the expressions Prospectus Directive means Directive
2003/71/ EC and includes any relevant implementing measure in
each Relevant Member State.
The underwriter and its affiliates have
performed investment banking, banking and/or advisory services
for us from time to time for which they have received customary
fees and expenses. The underwriter and its affiliates may, from
time to time, engage in other transactions with and perform
other services for us in the ordinary course of business.
A prospectus supplement in electronic
format may be made available on the website maintained by the
underwriter. In addition, shares may be sold by the underwriter
to securities dealers who resell shares to online brokerage
account holders.
We have agreed to indemnify the
underwriter against certain liabilities, including liabilities
under the Securities Act of 1933, as amended, or to contribute
to payments the underwriter may be required to make because of
any of those liabilities.
S-7
VALIDITY OF SECURITIES
Certain legal matters in connection with
this offering will be passed upon for us by Skadden, Arps,
Slate, Meagher & Flom LLP, New York, New York. Certain
legal matters in connection with this offering will be passed
upon for the underwriter by Ropes & Gray LLP.
WHERE YOU CAN FIND MORE
INFORMATION
We file reports, proxy statements, and
other information with the SEC. The public may read and copy any
materials filed by us at the SECs public reference room at
100 F Street, N.E., Washington, D.C. 20549 or on
the Internet site maintained by the SEC at http://www.sec.gov.
Please call the SEC at
1-800-SEC-0330 for
further information on the public reference room.
The SEC allows us to incorporate by
reference the information we file with them. This permits
us to disclose important information to you by referring to
these filed documents. Any information referred to in this way
is considered part of this prospectus supplement and
accompanying prospectus. We incorporate by reference the
following documents that have been filed with the SEC:
|
|
|
|
|
our Annual Report on
Form 10-K for the
year ended December 31, 2005 filed with the SEC on
February 28, 2006; |
|
|
|
our Quarterly Reports on
Form 10-Q for the
quarter ended March 31, 2006 filed with the SEC on
May 8, 2006, for the quarter ended June 30, 2006 filed
with the SEC on August 8, 2006, and for the quarter ended
September 30, 2006 filed with the SEC on November 6,
2006; and |
|
|
|
our Current Reports on
Form 8-K filed
with the SEC on April 19, 2006, May 2, 2006,
June 1, 2006, June 9, 2006, September 8, 2006,
October 18, 2006 and October 31, 2006. |
Any information in any of the foregoing
documents will automatically be deemed to be modified or
superceded to the extent that information in this prospectus or
in a later filed document that is incorporated or deemed to be
incorporated herein by reference modifies or replaces such
information.
We also incorporate by reference any
future filings (other than current reports furnished under
Item 2.02 or Item 7.01 of
Form 8-K and
exhibits filed on such form that are related to such items) made
with the SEC pursuant to Sections 13(a), 13(c), 14 or 15(d)
of the Securities Exchange Act of 1934, as amended (the
Exchange Act). Information in such future filings
updates and supplements the information provided in this
prospectus supplement and accompanying prospectus.
We will provide to each person, including
any beneficial owner, to whom a prospectus is delivered, without
charge upon written or oral request, a copy of any or all of the
documents that are incorporated by reference into this
prospectus, other than exhibits which are specifically
incorporated by reference into such documents. Requests should
be directed to the Investor Relations Department at Regeneron
Pharmaceuticals, Inc., 777 Old Saw Mill River Road, Tarrytown,
New York 10591 or by calling us at 914-345-7400.
S-8