By Catherine Eckford (European Pharmaceutical Review) and Dr Alaa Hamed (Sanofi)2024-09-12T15:21:18
In this article, Dr Alaa Hamed, Global Head of Medical Affairs for Rare Disease at Sanofi, shares why the company’s enzyme replacement therapy Xenpozyme® (olipudase alfa) has promise for the rare genetic disease acid sphingomyelinase deficiency (ASMD).
Already a member? Sign-in
European Pharmaceutical Review delivers authoritative insights, cutting-edge innovations, and expert perspectives that not only inform decisions but drive measurable progress across quality, compliance, and operational excellence.
By becoming a member you join a connected and collaborative community driving the industry forward. Member benefits include:
2026-04-14T12:32:00Z
Sponsored by Thermo Fisher Scientific
2026-04-14T12:29:00Z
Sponsored by JRS Pharma, In association with Vetter Pharma
2026-04-29T14:00:00Z 2026-04-29T15:00:00Z
Sponsored by USP
2026-05-27T13:00:00Z 2026-05-27T14:00:00Z
Sponsored by TA Instruments
2025-05-30T09:22:00
Sponsored by Lonza QC Testing Solutions
2025-06-26T08:43:00
Sponsored by Uniphar, By Tom Smith (Uniphar)
2025-12-11T13:32:00
Sponsored by Hexagon
2025-06-03T13:35:00
Sponsored by bioMérieux, By European Pharmaceutical Review
Site powered by Webvision Cloud