Gene transfer in hemophilia A: not cogent yet

Author:

Mannucci Pier Mannuccio

Abstract

The phase 3 clinical study of gene transfer in hemophilia A using the BioMarin vector AAV5-hFVIII-SQ (also identified as valoctocogene roxaparvovec) recently reported the results obtained in as many as 134 adult men with severe hemophilia A, so that it is at the moment the largest gene transfer study ever conducted in a rare monogenic disorder [...].

Publisher

PAGEPress Publications

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The evolving landscape of gene therapy for congenital severe hemophilia: a 2024 state of the art;Bleeding, Thrombosis and Vascular Biology;2024-09-04

2. Growing weapons to fight hemophilia;Bleeding, Thrombosis, and Vascular Biology;2023-02-23

3. Gentherapie mit AAV-Vektor reduziert Blutungen langanhaltend bei Hämophilie A;InFo Hämatologie + Onkologie;2022-07-28

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