Peregrine Pharmaceuticals Regains Full Compliance With Nasdaq Continued Listing Requirements
November 03 2009 - 3:00PM
PR Newswire (US)
TUSTIN, Calif., Nov. 3 /PRNewswire-FirstCall/ -- Peregrine
Pharmaceuticals, Inc. (NASDAQ:PPHMD) today announced that on
November 3, 2009, the Company received notice from the NASDAQ
Market Listing Qualifications Department stating that it has
regained compliance with the minimum bid price rule for the
continued listing of its common stock on the NASDAQ Capital Market,
as set forth in NASDAQ Marketplace Rule 5550(a)(2). Pursuant to
NASDAQ's rules, Peregrine was required to evidence a closing bid
price of at least $1.00 per share for 10 consecutive trading days.
The letter received from NASDAQ confirms that this requirement has
been met and that Peregrine is now in full compliance with all
NASDAQ continued listing requirements. As a result, Peregrine's
shares will continue to trade on the NASDAQ Capital Market. About
Peregrine Pharmaceuticals Peregrine Pharmaceuticals, Inc. is a
biopharmaceutical company with a portfolio of innovative monoclonal
antibodies in clinical trials for the treatment of cancer and
serious viral infections. The company is pursuing three separate
clinical programs in cancer and HCV infection with its lead product
candidates bavituximab and Cotara®. Peregrine also has in-house
manufacturing capabilities through its wholly owned subsidiary Avid
Bioservices, Inc. (http://www.avidbio.com/), which provides
development and biomanufacturing services for both Peregrine and
outside customers. Additional information about Peregrine can be
found at http://www.peregrineinc.com/. Safe Harbor Statement:
Statements in this press release which are not purely historical,
including statements regarding Peregrine Pharmaceuticals'
intentions, hopes, beliefs, expectations, representations,
projections, plans or predictions of the future are forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995. Factors that could cause actual results to
differ materially or otherwise adversely impact the company's
ability to obtain regulatory approval for its product candidates
include, but are not limited to, uncertainties associated with
completing preclinical and clinical trials for our technologies;
the early stage of product development; the significant costs to
develop our products as all of our products are currently in
development, preclinical studies or clinical trials; obtaining
additional financing to support our operations and the development
of our products; obtaining regulatory approval for our
technologies; anticipated timing of regulatory filings and the
potential success in gaining regulatory approval and complying with
governmental regulations applicable to our business. Our business
could be affected by a number of other factors, including the risk
factors listed from time to time in the company's SEC reports
including, but not limited to, the annual report on Form 10-K for
the year ended April 30, 2009 and the quarterly report on Form 10-Q
for the quarter ended July 31, 2009. The company cautions investors
not to place undue reliance on the forward-looking statements
contained in this press release. Peregrine Pharmaceuticals, Inc.
disclaims any obligation, and does not undertake to update or
revise any forward-looking statements in this press release.
Contacts: GendeLLindheim BioCom Partners Investors Media Barbara
Lindheim (800) 987-8256 (212) 918-4650 DATASOURCE: Peregrine
Pharmaceuticals, Inc. CONTACT: Investors, GendeLLindheim BioCom
Partners, 1-800-987-8256, ; or Media, Barbara Lindheim,
+1-212-918-4650, for Peregrine Pharmaceuticals, Inc. Web Site:
http://www.peregrineinc.com/ http://www.avidbio.com/
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