drugset / Trial / NCT02239224

Safety, Tolerability, Pharmacokinetics, and Biological Activity of ATYR1940 in Adult Participants With Muscular Dystrophy

NCT02239224 ↗

Phase 1/2 Completed 20 enrolled aTyr Pharma, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety and tolerability profile of ATYR1940 in the treatment of adult participants with molecularly defined genetic muscular dystrophies

Timeline

Start
2014-09-04
Primary completion
2015-12-14
Completion
2015-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject ATYR1940 Unknown 0.3 mg/kg Intravenous
Subject ATYR1940 Unknown 1 mg/kg Intravenous
Subject ATYR1940 Unknown 3 mg/kg Intravenous