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FDA panel votes against omapatrilat for hypertension
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Mon, 22 Jul 2002 19:00:00 Bethesda, MD - In a 5-1 vote, the Cardiovascular and Renal Drugs Advisory Committee to the FDA recommended against approval of Bristol-Myers Squibb's (BMS) vasopeptidase inhibitor omapatrilat (Vanlev®) for the treatment of hypertension. The panel was unconvinced that BMS had provided sufficient evidence that the antihypertensive benefit outweighed the high risk of angioedema. It did, however, leave open the option that the company could convince it in the future. |
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(2025-6-4)