drugset / Trial / NCT00506012

Pilot Efficacy Study of T2000 in Myoclonus Dystonia

NCT00506012 ↗

Phase 2 Terminated 5 enrolled Sun Pharmaceutical Industries, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This pilot study will evaluate the safety and efficacy of once daily T2000 when used to treat patients with Myoclonus Dystonia over a 12 week period.

Timeline

Start
2007-08
Primary completion
2011-08
Completion
2011-10

Outcome

Outcome not reported

Stopped (Enrollment): “Slow Recruitment of eligible patients”

Drugs

EvaluationDrugModalityDoseRoute
Subject T2000 Small molecule 1000 mg —

Indications