drugset / Trial / NCT02231580

Study Exploring Safety, Pharmacokinetic and Pharmacodynamic of BN82451 in Male Huntington's Disease Patients

NCT02231580 ↗

Phase 2 Terminated 17 enrolled Ipsen
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of BN82451B versus placebo after oral administration twice daily (bid) for 28 days in patients with Huntington's Disease (HD).

Timeline

Start
2014-09-01
Primary completion
2016-03-31
Completion
2016-03-31

Outcome

Outcome not reported

Stopped (Enrollment): “The study was terminated due to subject recruitment problems.”

Drugs

EvaluationDrugModalityDoseRoute
Subject BN82451B Unknown 40 mg Oral
Subject BN82451B Unknown 60 mg Oral
Subject BN82451B Unknown 80 mg Oral

Indications