ISTA Pharmaceuticals Highlights Bepreve(TM) Clinical Data at the Association for Research in Vision and Ophthalmology (ARVO) 2009 Annual Meeting
...
In another poster presentation titled "The Safety of the Anti-Histamine
bepotastine Besilate Ophthalmic Solution in a Healthy Pediatric Population from Ten to .... The results were presented in the following poster presentations:
bepotastine Besilate Ophthalmic Solution 1.0% Rapidly Reduces Conjunctival Hyperemia in...
ISTA Pharmaceuticals' New Drug Application for Bepreve(TM) Accepted for Review by U.S. Food and Drug Administration
...igns and symptoms of allergic conjunctivitis.
bepotastine was approved in Japan for use as a systemic drug i...sian countries, to develop, manufacture and market
bepotastine for ophthalmic use. In 2006, ISTA licensed the ex...an rights from Senju to an eye drop formulation of
bepotastine for the treatment of allergic conjunctivitis.
...
ISTA Pharmaceuticals Announces New Phase III Clinical Findings to Support Bepreve NDA Filing
...tive treatment against the signs and
symptoms of allergic conjunctivitis.
bepotastine was approved in Japan for use as a systemic drug in the
treatment of allerg...rom Senju the exclusive North
American rights to an eye drop formulation of
bepotastine for the treatment
of allergic conjunctivitis.
About ISTA Pharmaceuticals
...
Dr. Calvin Grant Presents Results from Xibrom(TM) Combination Therapy with Lucentis(R) at the 2008 Annual Meeting of the Association for Research in Vision and Ophthalmology (ARVO)
... uncertainties related to ISTA's research and development
programs (including without limitation the difficulty of predicting the
timing or outcome of
bepotastine product development efforts); the timing,
scope, and outcome of FDA or other regulatory agency approval or actions;
uncertainties and risks regarding ...
ISTA Pharmaceuticals Announces Physician-Sponsored Clinical Study of Xibrom(TM) Combination Therapy with Lucentis(R)
... uncertainties related to ISTA's research and development
programs (including without limitation the difficulty of predicting the
timing or outcome of
bepotastine product development efforts); the timing,
scope, and outcome of FDA or other regulatory agency approval or actions;
uncertainties and risks regarding ...
ISTA Pharmaceuticals Announces Statistically Significant
Preliminary Results From its U.S. Phase II/III Clinical Study Of
Bepotastine
...nalysis of its U.S. Phase II/III clinical study of
bepotastine for
the treatment of allergic conjunctivitis. The ...s of the study were the assessment of
efficacy for
bepotastine in treating ocular itching and redness.
The prelim...on of the second primary endpoint, ocular
redness,
bepotastine showed a trend toward clinical significance,
but d...
ISTA Pharmaceuticals Files New Drug Application with U.S. FDA for Bepreve(TM)
...e signs and symptoms of allergic conjunctivitis.
bepotastine was approved in Japan for use as a systemic drug i...sian countries, to develop, manufacture and market
bepotastine for
ophthalmic use. In 2006, ISTA licensed the exc...an rights
from Senju to an eye drop formulation of
bepotastine for the treatment of
allergic conjunctivitis.
Ab...