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Clinical Trial Summary

The primary objective of the study is to evaluate the long-term safety and tolerability of BIIB067 (tofersen) in participants with amyotrophic lateral sclerosis (ALS) and confirmed superoxide dismutase 1 (SOD1) mutation. The secondary objectives are to evaluate the pharmacokinetic (PK), pharmacodynamic (PD), biomarker effects, and efficacy of BIIB067 administered to participants with ALS and a confirmed SOD1 mutation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • ALS Caused by Superoxide Dismutase 1 (SOD1) Mutation

NCT number NCT03070119
Study type Interventional
Source Biogen
Contact
Status Active, not recruiting
Phase Phase 3
Start date March 8, 2017
Completion date August 12, 2024