Tuesday, June 17, 2008

Allergan Receives U.S. FDA Approval for Trivaris (triamcinolone acetonide injectable suspension) 80 mg/mL

June 17, 2008 - Allergan, Inc. today announced that the U.S. Food and Drug Administration (FDA) has approved Trivaris(TM) (triamcinolone acetonide injectable suspension) 80 mg/mL, a synthetic glucocorticoid corticosteroid with anti-inflammatory action. Delivered via intravitreal injection, the ophthalmic indications for TRIVARIS(TM) include sympathetic ophthalmia, temporal arteritis, uveitis, and ocular inflammatory conditions unresponsive to topical corticosteroids. These are inflammatory conditions that can result in vision loss.

"Retinal diseases are currently the leading cause of blindness in developed countries and represent a significant unmet need in eye care," said Scott Whitcup, M.D., Allergan's Executive Vice President, Research and Development. "TRIVARIS(TM) marks the first approval for Allergan resulting from our strategic focus on the development of therapies for back-of-the-eye diseases, and we remain committed to bringing forth innovative new treatments for patients suffering from retinal diseases."

The important safety information can be read here.

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