Current Releases
|
| Alcon Discontinues Development of Anecortave Acetate for Intraocular Pressure Reduction |
HUENENBERG, The Phase 2 study was rigorously designed to evaluate the safety and three-month IOP-lowering efficacy of a single anterior juxtascleral injection of three doses of anecortave acetate (24mg, 48mg and 60mg) versus vehicle. The mean reduction in IOP from baseline for the 60mg dose was 3.8 mmHg, which was statistically significant versus vehicle. The mean reduction in IOP was not statistically significant versus vehicle for the other doses. The goal of the study was to determine if different doses of anecortave acetate could provide IOP reduction similar to existing topical medications but for a period of three months with a single injection.
“The search for alternative delivery routes and new mechanisms of action
against glaucoma remain among Alcon’s most important research
strategies,” said
About
Caution Concerning Forward-Looking Statements.
This press release contains forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995. These
statements involve known and unknown risks, uncertainties and other
factors which may cause our actual results, performance or achievements
to be materially different from any future results, performances or
achievements expressed or implied by our forward-looking statements.
These statements reflect the views of our management as of the date of
this press release with respect to future events and are based on
assumptions and subject to risks and uncertainties. Given these
uncertainties, you should not place undue reliance on these
forward-looking statements. You should read this press release with the
understanding that our actual future results may be materially different
from what we expect. Except to the extent required under the federal
securities laws and the rules an regulations promulgated by the
Source:
Alcon Investor Relations |


