Following are the notable stock movers in the
biotech sector in the first hour:-
Arena Pharmaceuticals, Inc.(NASDAQ:ARNA) shares
gained 0.53% to $8.45 in the morning hour. Investment analysts at Credit Suisse
initiated coverage on shares of Arena Pharmaceuticals in a note issued to
investors on Sept. 6. The firm set an “underperform” rating and a $6.00 price
target on the stock. Additionally, analysts predict that ARNA will post $-0.26
earnings per share for the current fiscal year.
Will ARNA Move Back To new Highs? Find Out Here
Peregrine Pharmaceuticals(NASDAQ:PPHM) continued to
bounce back and added another 9% to $1.89 after recovering 46.50% in yesterday’s
session . On Monday, the stock was down 80% on news that previously released
results from a midstage cancer drug study aren't reliable because of a
third-party error in conducting the study. The news erased a tenfold increase
in the company's stock price this summer and removed almost a half-billion
dollars in market value for the Tustin, Calif., drug maker.
Will PPHM Continue To Move Higher? Find Out Here
Rosetta Genomics Ltd. (USA)(NASDAQ:ROSG) stock
gained 3.89% to $7.21. The company announced that Kenneth A. Berlin, President
and Chief Executive Officer of Rosetta Genomics, will present a corporate
update at the 2012 Aegis Healthcare Conference taking place from September
27-29, 2012 at The Wynn in Las Vegas, Nevada. Mr. Berlin's presentation will
take place on Saturday, September 29th at 10:00 a.m. Pacific time.
Sucampo Pharmaceuticals, Inc.(NASDAQ:SCMP) stock
climbed 16.61% to $5.28 after SCMP and Takeda Pharmaceuticals U.S.A., Inc.
announced that the U.S. Food and Drug Administration (FDA) has granted priority
review of their supplemental new drug application (sNDA) filing. The sNDA was
filed in late July seeking approval for an additional indication for AMITIZA
(lubiprostone) for the treatment of opioid-induced constipation (OIC) in
patients with chronic, non-cancer pain.
Cleveland BioLabs, Inc.(NASDAQ:CBLI) shares gained
0.35% to $2.88. The company, on Sept. 10, announced the receipt of an Advice
Letter from the U.S. Food and Drug Administration (FDA) indicating agreement
with proposed pivotal animal efficacy studies for the development of CBLB502 as
a radiation countermeasure. The FDA also accepted the Company's recently
concluded Good Laboratory Practice non-human primate (NHP) study as part of the
pivotal program.
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