drugset / Trial / NCT07195825

A Clinical Study to Evaluate the Safety, and Tolerability of BBM-P002 in the Treatment of Parkinson's Disease

NCT07195825 ↗

Phase 1 Recruiting 18 enrolled Shanghai Xinzhi BioMed Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the safety and tolerability of BBM-P002 for stereotactic injection to treat participants with idiopathic Parkinson's Disease (PD) during the dose-limiting toxicity (DLT) observation period.

Timeline

Start
2025-12-27
Primary completion
2027-12-30
Completion
2031-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject BBM-P002 Gene therapy (AAV / viral vector) — Other

Indications