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Avalglucosidase Alfa Betters Standard of Care for Late-Onstage Pompe Disease

Phase 3 COMET findings show the Sanofi Genzyme product delivered significantly improved efficacy and safety for the rare autosomal disorder. Investigational recombinant human lysosomal acid α-glucosidase (GAA) enzyme replacement therapy avalglucosidase alfa generated substantial clinical improvements in patients with late-onset Pompe disease (LOPD) versus alglucosidase alfa in new phase 3 findings.

Duke Clinical Research Update

SUPPORT OFFICE HOURS REDCap Office Hours   Email redcap-docr@duke.edu to schedule a virtual session at one of the times indicated below. Tuesdays 10 AM, virtual sessions Wednesdays 10 AM, virtual sessions Thursdays 2 PM, virtual sessions Fridays 10 AM, virtual sessions   SlicerDicer Office Hours Thursdays, 2 PM, via WebEx

Thought Leader Series — Dr. Vimal Mishra

Dr. Misra serves as Director of Digital Health for the American Medical Association (AMA). He is an associate professor of medicine and health administration at Virginia Commonwealth University Health System, specializing in internal medicine and health informatics.