FDA Says It Is Investigating Serious Malignancy Risk Linked To Zolgensma Gene Therapy
Nov 6 (Reuters) -
FDA - INVESTIGATES SERIOUS MALIGNANCY RISK LINKED TO ZOLGENSMA GENE THERAPY
FDA- CLOSELY MONITORING THE RISK OF NEOPLASIA, INCLUDING MALIGNANCY, IN OTHER SIMILAR AAV VECTOR-BASED GENE THERAPY PROGRAMS
FDA- THERE HAVE BEEN NO REPORTED CASES OF NEOPLASIA FOLLOWING ITVISMA ADMINISTRATION TO DATE
FDA- OVERALL BENEFITS OF ZOLGENSMA AND ITVISMA CONTINUE TO OUTWEIGH THEIR POTENTIAL RISKS FOR THEIR APPROVED USES
Source text: [ID: https://bit.ly/4zzunlF]
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