Pharmaceutical Business review

FDA seeks additional data for PAS for Allergan’s RESTASIS multi-dose bottle

The FDA requested additional CMC information for the Multi-Dose Preservative-Free (MDPF) bottle, a first of its kind container with patented uni-directional valve and air filter technology.

Allergan is compiling the data requested and will respond to the FDA in a timely manner. In the absence of additional data requests from the FDA, Allergan does not anticipate a significant impact to previously communicated timelines of the potential approval of the MDPF bottle.

RESTASIS, approved by the U.S. Food and Drug Administration in 2002, is the only eye drop that helps increase the eyes’ natural ability to produce tears, which may be reduced by inflammation due to Chronic Dry Eye disease. RESTASIS did not increase tear production in patients using anti-inflammatory eye drops or tear duct plugs.

About Chronic Dry Eye

Chronic Dry Eye is caused by reduced tear production due to inflammation. Dry eye is often a chronic disease that can be caused by advanced age, contact lens wear, certain medications, eye diseases, other medical conditions, or environmental factors. Without enough tears, the film protecting the eye can break down, creating dry spots on the cornea.

About RESTASIS

RESTASIS helps increase the eyes’ natural ability to produce tears, which may be reduced by inflammation due to Chronic Dry Eye disease. RESTASIS did not increase tear production in patients using anti-inflammatory eye drops or tear duct plugs.