drugset / Trial / NCT02531217

Safety, Tolerability, Pharmacokinetics (PK), and Activity of ATYR1940 in Participants With Muscular Dystrophy - Study Extension

NCT02531217 ↗

Phase 1/2 Completed 9 enrolled aTyr Pharma, Inc.
NaSingle-groupOpen-labelTreatment

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
2015-08-13
Primary completion
2016-05-26
Completion
2016-05-26

Drugs

EvaluationDrugModalityDoseRoute
Subject ATYR1940 Unknown 3 mg/kg Intravenous