drugset / Trial / NCT05435729

A Pharmacodynamics and Safety Study of DSP-9632P in Patients With Levodopa-Induced Dyskinesia in Parkinson's Disease

NCT05435729 ↗

Phase 1 Completed 7 enrolled Sumitomo Pharma Co., Ltd.
RandomizedCrossoverQuadruple-blindTreatment

Summary

This study is an open-label of single transdermal dose of DSP-9632P to evaluate the dopamine release derived from levodopa in brain, and a randomized, double-blind, placebo-controlled, 2-way crossover of multiple transdermal doses of DSP-9632P to evaluate the safety and tolerability in patients with levodopa-induced dyskinesia in Parkinson's disease.

Timeline

Start
2022-05-31
Primary completion
2022-11-30
Completion
2022-12-02

Drugs

EvaluationDrugModalityDoseRoute
Subject DSP-9632P Unknown 27.5 mg Other
Subject DSP-9632P Unknown 55 mg Other
Subject DSP-9632P Unknown 82.5 mg Other
Background Levodopa formulation Unknown — —