Published: July 30, 2010
Board of Directors of Genta Incorporated Announce Reverse Split of Company's Common Stock
BERKELEY HEIGHTS, N.J. - (BUSINESS WIRE) - Genta Incorporated (OTCBB: GETA) announced today that its Board of
Directors has approved a one-for-one hundred reverse stock split of
Genta's common stock, and that the split will be effective with the open
of trading on August 2, 2010. As of that date, the Company's common
stock will temporarily trade under the symbol GETAD.OB for 20 business
days, at which time the symbol will revert to GETA.OB.
At the Annual Meeting of Stockholders held on June 15, 2010, Genta's
stockholders approved a proposal authorizing the Board of Directors, in
its discretion, to effect a reverse split of Genta's outstanding common
stock. Additional details regarding the reverse stock split are
contained in the Current Report on Form 8-K filed with the Securities
and Exchange Commission simultaneously herewith.
About Genta
Genta
Incorporated is a biopharmaceutical company with a diversified product
portfolio that is focused on delivering innovative
products for the treatment of patients with cancer. The Company is
developing tesetaxel,
a novel, orally absorbed taxane that is in the same class of drugs as
paclitaxel and docetaxel. As the leading oral taxane in clinical
development, tesetaxel
has completed several Phase 2 clinical trials. Genta has initiated a
broad program of clinical studies to evaluate the safety and efficacy of tesetaxel
in patients with solid tumors. The Company has announced that gastric
(stomach) cancer will be the lead indication for regulatory registration
of tesetaxel.
Genasense
(oblimersen sodium) Injection is a modified DNA-based antisense drug
that may enhance the effectiveness of anticancer therapy. Enrollment in
a randomized Phase 3 study of Genasense in patients with
advanced melanoma (the AGENDA trial) has been completed. Long-term data
on durable response and survival from AGENDA, which if positive may
provide a basis for regulatory approval, are expected in 2011. Genta is
exclusively marketing Ganite
(gallium nitrate injection) in the U.S, which is indicated for
treatment of symptomatic patients with cancer-related hypercalcemia that
is resistant to hydration. The Company has developed proprietary oral
formulations of the active ingredient in Ganite that are
being evaluated as potential treatments for diseases associated with
accelerated bone loss. Ganite and Genasense® are
available on a "named-patient" basis in countries outside the United
States. For more information about Genta,
please visit our website at: www.genta.com.
Safe Harbor
This press release may contain forward-looking statements with
respect to business conducted by Genta
Incorporated. By their nature, forward-looking statements and forecasts
involve risks and uncertainties because they relate to events and depend
on circumstances that will occur in the future. Such
forward-looking statements include those that express plan,
anticipation, intent, contingency, goals, targets, or future
developments and/or otherwise are not statements of historical fact. The
words "potentially" , "anticipate" , "could" , "calls for" , and similar
expressions also identify forward-looking statements. The Company
does not undertake to update any forward-looking statements. Factors
that could affect actual results include, without limitation, risks
associated with:
-
the Company's ability to obtain necessary regulatory approval for
its product candidates from regulatory agencies, such as the U.S. Food
and Drug Administration and the European Medicines Agency;
-
the safety and efficacy of the Company's products or product
candidates;
-
the commencement and completion of any clinical trials;
-
the Company's assessment of its clinical trials;
-
the Company's ability to develop, manufacture, license, or sell its
products or product candidates;
-
the Company's ability to enter into and successfully execute any
license and collaborative agreements;
-
the adequacy of the Company's capital resources and cash flow
projections, or the Company's ability to obtain sufficient financing
to maintain the Company's planned operations;
-
the adequacy of the Company's patents and proprietary rights;
-
the impact of litigation that has been brought against the Company;
and
-
the other risks described under Certain Risks and Uncertainties
Related to the Company's Business, as contained in the Company's
Annual Report on Form 10-K and Quarterly Report on Form 10-Q.
There are a number of factors that could cause actual results and
developments to differ materially. For a discussion of those
risks and uncertainties, please see the Company's Annual Report on Form
10-K for 2009 and its most recent quarterly report on Form 10-Q.

Genta Investor Relations
908-286-3980
info@genta.com
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