CSL’s Hemgenix Gene Therapy Does Not Need A REMS, FDA Tells National Hemophilia Foundation

Peter Marks says labeling for CSL’s hemophilia B treatment adequately conveys its risks. He also denies NHF request that the label cite eligibility criteria used in clinical trials, responding to a citizen petition on the day the agency approves the therapy.

Gene therapy
Labeling for hemophilia gene therapy infusion sufficiently conveys risks of its use, US FDA says • Source: Shutterstock

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