Tricida (TCDA) Says FDA Accepts Veverimer NDA

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Go back to Tricida (TCDA) Says FDA Accepts Veverimer NDA

Tricida Announces FDA Acceptance of New Drug Application for Veverimer

November 14, 2019 4:03 PM EST

SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)-- Tricida, Inc. (Nasdaq: TCDA), a pharmaceutical company focused on the development and commercialization of its drug candidate, veverimer (TRC101), a non-absorbed, orally-administered polymer designed to treat metabolic acidosis in patients with chronic kidney disease (CKD), announced today that the U.S. Food and Drug Administration (FDA) has accepted for review its New Drug Application (NDA) for veverimer under the Accelerated Approval Program. In its correspondence, FDA also stated that no filing review issues were identified. The FDA has assigned a Prescription Drug User Fee Act (PDUFA)... More