Project Details
Description
A Phase 2b/3, Double-blind, Randomized, Placebo-Controlled, Multicenter Study to Assess the Efficacy and Safety of VX-210 in Subjects With Acute Traumatic Cervical Spinal Cord Injury
Status | Finished |
---|---|
Effective start/end date | 9/1/16 → 2/28/19 |
Funding
- Vertex Pharmaceuticals Incorporated
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