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Rocket Pharmaceuticals: FDA Grants Priority Review For RP-L201

Rocket Pharmaceuticals, Inc. (RCKT) announced the FDA has accepted the Biologics License Application and granted Priority Review for RP-L201, a lentiviral vector-based investigational gene therapy for severe Leukocyte Adhesion Deficiency-I.

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Invitae's First of Its Kind Cancer Test Receives FDA Marketing Authorization

The FDA awarded marketing authorization for a new Invitae test that uses next-generation sequencing to assess multiple genes to identify variants indicating a person’s predisposition for certain cancers. The regulatory action creates a new regulatory classification making Invitae’s test the predicate device for future cancer tests.

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Why Is Genetic Testing Invitae Stock Trading Higher Today?

Friday, the FDA granted de novo approval for Invitae Corporation's NVTA Common Hereditary Cancers Panel, an in vitro diagnostic test that can help detect…

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