drugset / Trial / NCT04691661

Safety, Tolerability, Pharmacokinetics and Efficacy Study of Radotinib in Parkinson's Disease

NCT04691661

Phase 2 Recruiting 40 enrolled Il-Yang Pharm. Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a safety, tolerability, pharmacokinetic and efficacy study in subjects with Parkinson's disease

Timeline

Start
2021-09-09
Primary completion
2025-12-31
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Radotinib Small molecule 50 mg Oral
Subject Radotinib Small molecule 100 mg Oral
Subject Radotinib Small molecule 150 mg Oral
Subject Radotinib Small molecule 200 mg Oral

Indications