Eyetech Pharmaceuticals, Inc.

U.S. FDA approves Macugen for treatment of neovascular wet AMD

Published in Biotech Law Weekly, January 21st, 2005

Eyetech Pharmaceuticals, Inc., (EYET) and Pfizer, Inc., (PFE) announced that the U.S. Food and Drug Administration (FDA) approved Macugen (pegaptanib sodium injection) for the treatment of neovascular (wet) age-related macular degeneration (AMD), an eye disease associated with aging that destroys central vision.

Macugen helps preserve vision and helps limit progression to legal blindness. Approval of Macugen follows a priority review under the FDA's rolling submission-Pilot 1 program based on data from the companies' phase II/III pivotal clinical trials.

Macugen is the first in a new class of ophthalmic drugs to specifically target vascular...

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Source: Biotech Law Weekly (2005-01-21)

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