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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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