drugset / Trial / NCT04571164

A Study to Evaluate the Effectiveness and Safety of LY03003 in Patients With Early Primary PD

NCT04571164 ↗

Phase 3 Completed 294 enrolled Luye Pharma Group Ltd. Parexel · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is to evaluate the effictiveness and safety of Ly03003 following intramuscular injections

Timeline

Start
2020-05-11
Primary completion
2022-03-17
Completion
2022-09-27

Outcome

Met primary endpoint

release “LY03003)治 疗 帕 金 森 病 的 中 国Ⅲ期 临 床 试 验 达 到 预 设 终 点” luye.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject LY03003 Unknown 56 mg Intramuscular

Indications