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Clinical Trials in China / NCT06978920
Recruiting Phase 1

A Trial to Evaluate the Safety, Tolerability and Preliminary Efficacy of NCR201 in the Treatment of Subjects With Parkinson's Disease

NCT06978920 · tracked via the Priya Life Science China tracker
Sponsor
Nuwacell Biotechnologies Co., Ltd.
Phase
Phase 1
Started
2025-06-06
Last updated
2025-08-01

Condition(s) studied

Parkinson Disease

Investigational drug(s) / intervention(s)

Allogeneic dopaminergic neural precursor cell(NCR201)

Allogeneic dopaminergic neural precursor cell(NCR201): Bilateral implantation

Study summary

The goal of this clinical trial is to evaluate the safety, tolerability and preliminary efficacy that NCR201 has on Parkinson's disease (PD) patients.

Eligibility

Sex
ALL
Min age
40 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Ages between 40 and 75 years; * Diagnosed to be Parkinson's disease according to Parkinson's disease diagnostic criteria; * Disease history over 5 years; * Stable dose of dopamine treatment; * Able to undergo PET/CT/MRI detection; Exclusion Criteria: * Patients who have previously undergone brain surgery; * Past use of stem cell therapy or participation in stem cell clinical research; * Cognitive impairment; * History of mental disorders; * Patients with other serious systemic diseases; * Past or current metastatic malignant tumors.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of USTC Hefei Anhui Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06978920 on ClinicalTrials.gov ↗ ← All trials in China