drugset / Trial / NCT02074410

Safety and Efficacy of OMS643762 in Subjects With Huntington's Disease

NCT02074410 ↗

Phase 2 Terminated 22 enrolled Omeros Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety, tolerability and pharmacokinetics of OMS643762 (the study drug) in subjects with Huntington's disease (HD).

Timeline

Start
2014-01
Primary completion
2014-10-15
Completion
2014-10-15

Outcome

Outcome not reported

Stopped (Business): “Sponsor decision - pending further analysis of available data”

Drugs

EvaluationDrugModalityDoseRoute
Subject OMS643762 Unknown — Oral

Indications