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Study of AAV-hSMN1 (Vesemnogene Lantuparvovec) Gene Therapy in Subjects with Progressive Spinal Muscular Atrophy

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Trial Profile

Study of AAV-hSMN1 (Vesemnogene Lantuparvovec) Gene Therapy in Subjects with Progressive Spinal Muscular Atrophy

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 14 Oct 2024

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At a glance

Most Recent Events

  • 09 Oct 2024 Planned End Date changed from 30 Jul 2027 to 30 Oct 2027.
  • 09 Oct 2024 Planned primary completion date changed from 30 Jul 2027 to 30 Oct 2027.
  • 09 Oct 2024 Planned initiation date changed from 30 Jul 2024 to 20 Oct 2024.

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