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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03309514
Other study ID # NGN-9076
Secondary ID
Status Withdrawn
Phase Phase 1/Phase 2
First received
Last updated
Start date June 2022
Est. completion date June 30, 2024

Study information

Verified date April 2022
Source NeuroGeneration
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a prospective study to demonstrate the safety and efficacy of differentiated neurons-derived from adult CNS progenitors cells transplanted in selected patients with Parkinson's disease.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 30, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 35 Years to 85 Years
Eligibility Inclusion Criteria: 1. Able to give informed consent prior to study 2. Male or Female with Diagnostic Criteria of Parkinson's disease 3. Age 35 to 85 years old 4. Parkinson's disease not due to trauma, infection, brain tumor, cerebrovascular disease 5. Hoehn and Yahr Stage III or IV 6. Parkinson's disease observed in the absence of: - Oculomotor palsy - Cerebellar sign - Orthostatic hypotension (drop greater than 20mmHg in mean pressure) - Pyramidal sign - Amyotrophy 7. Good general health or stable medical condition well controlled, without contraindications to anesthesia Exclusion Criteria: 1. Patients with severe dementia and brain atrophy on MRI 2. Patients with severe hypertension; renal, liver, cardiac or other major organ disease; coagulopathy; cancer; other significant systemic illnesses; hepatitis, HIV 3. Patients older than 85 or younger than 35 4. Patients who withhold informed consent 5. Patients with a history of alcohol or drug abuse 6. Sexually active women of childbearing potential without adequate form of birth control 7. Evidence of abnormal coagulation or anticoagulant therapy 8. Pregnancy or lactation 9. History of seizure disorders or current use of antiepileptic medication 10. Severe cognitive impairment 11. Clinically significant laboratory abnormality

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Intracerebral microinjections
Stereotactic delivery of cell suspension into basal ganglia structures

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
NeuroGeneration

Outcome

Type Measure Description Time frame Safety issue
Primary Motor UPDRS UPDRS Motor scale 6 months
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