Achillion Announces ACH-4471 Granted Orphan Drug Designation for the Treatment of C3 Glomerulopathy (C3G) and the Initiation of a Phase 1 Extended-Release Bioavailability Study
ACHISON INC A (ACHN)
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Source: GlobeNewswire
- Orphan drug designation for the treatment of C3G granted by the U.S. Food and Drug Administration (FDA) – - Initiated bioavailability study evaluating extended-release formulations of ACH-4471 in healthy volunteers– NEW HAVEN, Conn., Dec. 18, 2017 (GLOBE NEWSWIRE) -- Achillion Pharmaceuticals, Inc. (Nasdaq:ACHN), a pharmaceutical company focused on advancing small molecule inhibitors of factor D in the complement alternative pathway, today announced the U.S. Food and Drug Administration (FDA) has granted orphan drug designation to ACH-4471 for the treatment of patients with C3 Glomerulopathy (C3G). C3G is a devastating renal disease for which there is no approved therapy. There are estimated to be approximately 4,000 C3G patients in the United States, approximately 4,000 in Europe, and more than 1,000 patients with this devastating disease in Japan. The FDA Orphan Drug Designation program provides incentives for the development of potentially promising drugs to treat, diagnose
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