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FDA Issues CRL for Patisiran in Treatment of ATTR Cardiomyop
FDA Issues CRL for Patisiran in Treatment of ATTR Cardiomyop
FDA Issues CRL for Patisiran in Treatment of ATTR Cardiomyopathy
Announced on October 9, the decision to issue a CRL is based on the FDA's belief the clinical meaningfulness of patisiran’s treatment effects for the cardiomyopathy of ATTR amyloidosis had not been established.
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