健康知识网 > 健康知识 > 健康资讯 > 血友病基因疗法达到3期临床终点 预计第三季度递交监管申请(2)

血友病基因疗法达到3期临床终点 预计第三季度递交监管申请(2)

发表日期:2019-08-16 12:23 | 来源 :原创整理 | 点击数: 次 收听:

参考资料:

[1] BioMarin Announces that Phase 3 Cohort of Valoctocogene Roxaparvovec, Gene Therapy Study in Severe Hemophilia A Met Pre-Specified Criteria for Regulatory Submissions in the U.S. and Europe. Retrieved May 28, 2019, from https://investors.biomarin.com/2019-05-28-BioMarin-Announces-that-Phase-3-Cohort-of-Valoctocogene-Roxaparvovec-Gene-Therapy-Study-in-Severe-Hemophilia-A-Met-Pre-Specified-Criteria-for-Regulatory-Submissions-in-the-U-S-and-Europe

[2] BioMarin Provides 3 Years of Clinical Data from Ongoing Phase 1/2 Study of Valoctocogene Roxaparvovec Gene Therapy for Severe Hemophilia A. Retrieved May 28, 2019, from https://investors.biomarin.com/2019-05-28-BioMarin-Provides-3-Years-of-Clinical-Data-from-Ongoing-Phase-1-2-Study-of-Valoctocogene-Roxaparvovec-Gene-Therapay-for-Severe-Hemophilia-A

*声明:本文由入驻新浪医药新闻作者撰写,观点仅代表作者本人,不代表新浪医药新闻立场。

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