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Compass Pathways announces FDA granted NDA rolling review request

Compass Pathways (CMPS) announced the U.S. Food and Drug Administration granted Compass NDA rolling review request and selected COMP360, Compass’ proprietary formulation of synthetic psilocybin, for the Commissioner’s National Priority Voucher program for treatment-resistant depression. “Companies selected for the voucher program will be entitled to benefits including enhanced communications and a shortened 1-2 month review time following filing of a New Drug Application, while maintaining FDA’s rigorous safety and efficacy standards,” the company stated.

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