Live Breaking News & Updates on Central committee on research involving human subjects

SwanBio Therapeutics: SwanBio Advances to Higher-Dose Cohort in First-in-Human Study of Gene Therapy for Adrenomyeloneuropathy

SwanBio Therapeutics: SwanBio Advances to Higher-Dose Cohort in First-in-Human Study of Gene Therapy for Adrenomyeloneuropathy
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SwanBio Advances to Higher-Dose Cohort in First-in-Human Study of Gene Therapy for Adrenomyeloneuropathy

PHILADELPHIA (BUSINESS WIRE) Oct 4, 2023

Netherlands , United-states , United-kingdom , Italy , France , Spain , Germany , David-weiner , Lara-furst , Chris-hollowood , European-medicines-agency , Central-committee-on-research-involving-human-subjects

Syncona : SwanBio Advances to Higher-Dose Cohort in First-in-Human Study of Gene Therapy for Adrenomyeloneuropathy -October 04, 2023 at 07:28 am EDT

Independent Data Safety Monitoring Board recommended dose escalation

First patient in cohort 2 has received SBT101

Majority investor Syncona providing new.

Netherlands , Italy , United-kingdom , France , United-states , Germany , Spain , Chris-hollowood , Lara-furst , David-weiner , European-medicines-agency , Central-committee-on-research-involving-human-subjects

In review: the life sciences regulatory regime in Netherlands

This article reviews the essential regulatory considerations surrounding medicines and medical devices in Netherlands, including clinical trials and marketing authorisations.

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European law could improve 'scandalous' lack of clinical trial data reporting | Science

European law could improve 'scandalous' lack of clinical trial data reporting | Science
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