2008-08-06 10:15:00
VIVUS Announces Closing of $65 Million Registered Direct Offering of Common Stock
MOUNTAIN VIEW, Calif.–(EMWNews)–VIVUS, Inc. (NASDAQ: VVUS) announced today that it has consummated the
previously announced registered direct offering of 8,365,508 shares of
its common stock to a select group of institutional investors at $7.77
per share. The offering resulted in net proceeds of approximately $63.4
million.
The shares described above were offered by VIVUS pursuant to a
registration statement previously filed and declared effective by the
Securities and Exchange Commission on May 29, 2008.
“We are pleased that we were able to involve a
group of high-quality, new and existing investors in this financing,”
said Leland Wilson, president & CEO of VIVUS. “We
look forward to being able to use the proceeds of the offering to
advance our late stage investigational product candidates, including
Qnexa that is under clinical development to treat obesity and diabetes.”
This press release shall not constitute an offer to sell or the
solicitation of an offer to buy any of the securities described herein,
nor shall there be any sale of these securities in any state or
jurisdiction in which such offer, solicitation or sale would be unlawful
prior to registration or qualification under the securities laws of any
such state or jurisdiction. Copies of the prospectus supplement and
accompanying base prospectus relating to this offering may be obtained
at the SEC’s website at http://www.sec.gov.
About VIVUS
VIVUS, Inc. is a pharmaceutical company dedicated to the development and
commercialization of novel therapeutic products. The current portfolio
includes investigational product candidates under development to address
obesity, diabetes and sexual health, including: Qnexa™,
for which phase 3 studies for the treatment of obesity have been
initiated and a phase 2 study for the treatment of type 2 diabetes has
been completed; Luramist™ (Testosterone MDTS®),
for which a phase 2 study has been completed for the treatment of
Hypoactive Sexual Desire Disorder (HSDD); and avanafil, for which a
phase 2 study has been completed for the treatment of erectile
dysfunction (ED). MUSE® is approved and
currently on the market for the treatment of ED. For more information on
clinical trials and products, please visit the company’s
web site at http://www.vivus.com/.
Certain statements in this press release are forward-looking within
the meaning of the Private Securities Litigation Reform Act of 1995.
These statements may be identified by the use of forward-looking words
such as “anticipate,” “believe,” “forecast,” “estimated” and “intend,”
among others. These forward-looking statements are based on VIVUS’
current expectations and actual results could differ materially. There
are a number of factors that could cause actual events to differ
materially from those indicated by such forward-looking statements.
These factors include, but are not limited to, substantial competition;
uncertainties of patent protection and litigation; uncertainties of
government or third party payer reimbursement; reliance on sole source
suppliers; limited sales and marketing efforts and dependence upon third
parties; risks related to the development of innovative products; and
risks related to failure to obtain FDA clearances or approvals and
noncompliance with FDA regulations. As with any pharmaceutical under
development, there are significant risks in the development, regulatory
approval and commercialization of new products. There are no guarantees
that future clinical studies discussed in this press release will be
completed or successful or that any product will receive regulatory
approval for any indication or prove to be commercially successful.
VIVUS does not undertake an obligation to update or revise any
forward-looking statement. Investors should read the risk factors set
forth in VIVUS’ Form 10-K for the year ended December 31, 2007 and
periodic reports filed with the Securities and Exchange Commission.
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VIVUS, Inc. Financial Officer (SF), 415-392-3385 |
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