SOURCE: Ohr Pharmaceutical Inc.
November 23, 2009 09:00 ET
Ohr Pharmaceutical (OTC BB: OHRP) Data Review Supports Strong Potential of EVIZON™ for Wet AMD
DOVER, DE--(Marketwire - November 23, 2009) - As part of its drug pipeline Ohr Pharmaceutical
(OTCBB: OHRP) is developing a wet AMD (Macular Degeneration) therapy, based
on technology acquired from Genaera Liquidating Trust. This novel
therapeutic agent (EVIZON™) has demonstrated the improvement or
stabilization in vision in more than 100 subjects with wet AMD. Patients
(wet AMD subjects) treated with at least 40 mg/m2 of EVIZON in phase 1 and
2 studies demonstrated early signs of a biological effect: 18% had three
lines or greater improvement in visual acuity 4 months after they had
completed therapy and another 72% had stable vision. Throughout its
clinical development, the drug was well tolerated, with no drug-related
serious adverse events occurring in patients involved in this trial.
EVIZON™ (Squalamine for wet AMD) is a systemic anti-angiogenic therapy
with a novel mechanism of action which avoids the cardiovascular and
ophthalmic side effects associated with intraocular injections of anti-VEGF
antibodies. As evidence of this advantage, there were no clinically
significant increases in systolic or diastolic blood pressure in clinical
studies of 124 wet AMD subjects receiving EVIZON in Phase 2 clinical
trials.
Wet AMD is the leading cause of legal blindness among adults age 50 or
older in the Western world. Age-related macular degeneration is a
progressive disease which is characterized the early stage "dry" form and
the more severe "wet" form. Wet AMD is caused by the growth of abnormal
blood vessels, or choroidal neovascularization, under the central part of
the retina, the macula. Although the wet form of AMD accounts for only 10%
to 15% of all AMD, it is responsible for 90% of severe vision loss
associated with AMD. Approximately 500,000 new cases of wet AMD are
diagnosed annually worldwide. In North America alone, approximately 200,000
new cases of wet AMD are diagnosed each year.
Recognizing the significant therapeutic potential of EVIZON™, Ohr
Pharmaceutical is developing a promising novel formulation to enhance its
bioavailability while maintaining its excellent safety profile.
About Ohr Pharmaceutical, Inc.
Ohr Pharmaceutical, Inc. (www.ohrpharmaceutical.com) (OTCBB: OHRP) is a
biotechnology company dedicated to the development of first in class drugs
for underserved therapeutic needs. Ohr is focused on the development of two
drugs, OHR/AVR118 for the treatment of Cachexia and EVIZON for the
treatment of wet-AMD.
Approval of Pharmaceutical Products
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the efficacy of pharmaceutical products can be claimed or assured until
final testing; and no assurance or warranty can be made that the FDA will
approve final testing or marketing of any pharmaceutical product.
Safe Harbor Statement under the Private Securities Litigation Reform Act of
1995:
This news release contains forward-looking statements within the meaning of
the "safe harbor" provisions of the Private Securities Litigation Reform
Act of 1995. These forward looking statements are made only as the date
thereof, and Ohr undertakes no obligation to update or revise the forward
looking statement whether as a result of new information, future events or
otherwise. Our actual results may differ materially and adversely from
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change in our markets, changes in demand for our future products,
legislative, regulatory and competitive developments, the financial
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there can be no assurance that Ohr will be able to sustain operations for
expected periods, or that we will be able to achieve or sustain targeted
levels of expense reductions. Ohr's most recent Annual Report and
subsequent Quarterly Reports discuss some of the important risk factors
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condition. We disclaim any intent to revise or update publicly any
forward-looking statements for any reason.