Intermediate Size Patient Population Expanded Access IND for the Treatment of Patients With Parkinson's Disease.

Status:

NO_LONGER_AVAILABLE

Intermediate Size Patient Population Expanded Access IND for the Treatment of Patients With Parkinson's Disease.

Lead Sponsor:

Hope Biosciences Research Foundation

Conditions:

Parkinson Disease

Eligibility:

All Genders

76-95 years

Brief Summary

This Expanded Access IND is to evaluate the safety of multiple intravenous administrations of HB-adMSCs for treating Parkinson's disease in 10 patients between 76 and 95 y/o who do not qualify for oth...

Detailed Description

This expanded access program is designed to include adult male and female outpatients with Parkinson's disease with ages between 76 and 95 y/o. -Screening During the Screening Visit, each patient who...

Eligibility Criteria

Inclusion

Inclusion Criteria
A participant will be eligible for inclusion in this expanded access program only if all the following criteria apply:
Patients aged 76-95 years old (male and female).
Patients must have had a Parkinson's disease diagnosis for a minimum of six months before 1st infusion.
Patients must have previously banked their mesenchymal stem cells with Hope Biosciences.
Patients should be able to read, understand, and provide voluntarily written consent.
Patients able and willing to comply with the requirements of this expanded access program.
Exclusion Criteria
A participant will not be eligible for inclusion in this expanded access program if any of the following criteria apply:
Patients with advanced Parkinson's disease. Advanced PD is defined as a significant disability, wheelchair-bound or bedridden.
Any malignancy or clinical evidence that supports the presence of a malignant process in a patient is being investigated. Malignancy is defined as any form of cancer that had occurred in the previous five years before the first infusion and may require surgery, chemotherapy, or radiation.
Patients with medical history of uncontrolled high blood pressure defined as a deficient standard of care treatment and/or blood pressure \> 140/90 mm/Hg during screening visit.
Patients with the following concomitant or past medical history:
Heart Failure - New York Heart Association (NYHA) Class III/IV.
Heart Attack (in the past six months before 1st infusion).
Stroke (in the past six months before 1st infusion).
Hepatitis B or C.
Human immunodeficiency virus (HIV) infection.
Any of the following abnormal lab findings during screening will disqualify a patient from this expanded access program:
Hemoglobin (Hgb) \<10 G/DL or \>18 G/DL
Hematocrit (HCT) \<30% or \>54 %
Platelet count \< 80 K/UL and or \> 450 K/UL.
White blood cell count WBC \< 3.0 K/UL and \> 12.0 K/UL.
Alanine aminotransferase (ALT) of \> 75 IU/L
Aspartate aminotransferase (AST) of \> 75 IU/L
eGFR \< 59 mL/min/1.73
Pre-prandial glucose \> 130 MG/DL
Post-prandial glucose \> 200 MG/DL
Patients who have received any stem cell treatment in the past six months before 1st infusion other than stem cells produced by Hope Biosciences.
Patients who are unlikely to complete the visits or adhere to the procedures.
The patient has previously been diagnosed with a psychiatric disorder, which is currently uncontrolled.
Patients with a history of addiction or dependency or currently abusing or using substances.
Patients with any form of kidney dialysis will be excluded from participation in the investigation.
Patients who have received an experimental drug in the past 12 months before the first dose of the investigational product. (Except for COVID-19 vaccinations).
Patients who the Investigator determines to be unsuitable for participation for other reasons, such as, but not limited to deep vein thrombosis (DVT), pulmonary embolus, cardiac arrhythmia, or those who have a prothrombotic condition, or who require persistent oxygen supplementation.
Patients who have recently undergone major surgery (in the past six months before 1st infusion). Some examples of major surgeries include, but are not limited to, the following: heart surgeries, aortic aneurysm bypass, organ transplant, intracranial surgery, spinal laminectomy or fusion, amputation, resection of the lung, resection of esophagus, resection of a mediastinal mass, resection of bladder or prostate tumor and resection of kidney or ureter.

Exclusion

Key Trial Info

Start Date :

Trial Type :

EXPANDED_ACCESS

End Date :

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT04772378

Last Update

September 29 2025

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