drugset / Trial / NCT03956979

A Study in Parkinson's Disease in Patients With Moderate to Severe Dyskinesia

NCT03956979 ↗

Phase 2 Completed 89 enrolled Contera Pharma Bukwang Pharmaceutical · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The current study will explore the efficacy, safety and tolerability of 2 dose combinations of JM-010 to determine the optimal doses of each component to be studied in confirmatory clinical trials.

Timeline

Start
2019-07-22
Primary completion
2024-03-07
Completion
2024-03-21

Outcome

Missed primary endpoint

release “Unfortunately, the primary endpoint assessing reduction in dyskinesia as evaluated by the UDysRS was not met. The ASTORIA trial was well conducted” conterapharma.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject JM-010 Unknown 0.8 mg —
Subject JM-010 Unknown 8 mg —

Indications