| Eligibility |
Inclusion Criteria:
1. Patients must have passed pre-screening for the HBPD03 clinical trial entitled, "A
Randomized, Double-Blind, Single Center, Phase 2, Efficacy and Safety Study of
autologous HB-adMSCs vs Placebo for the Treatment of Patients with Parkinson's
Disease" under IND 027396.
2. Patients must have screened for the HBPD03 clinical trial entitled, "A Randomized,
Double-Blind, Single Center, Phase 2, Efficacy and Safety Study of autologous
HB-adMSCs vs Placebo for the Treatment of Patients with Parkinson's Disease" under IND
027396.
3. Patients must have not been randomized into the treatment group for the HBPD03
clinical trial entitled, "A Randomized, Double-Blind, Single Center, Phase 2, Efficacy
and Safety Study of autologous HB-adMSCs vs Placebo for the Treatment of Patients with
Parkinson's Disease" under IND 027396.
4. Male and female participants 18 - 80 years of age.
5. Patients must have been diagnosed with early and/or moderate Parkinson's disease at
least 6 months before participation.
6. Patients must have previously banked their mesenchymal stem cells with Hope
Biosciences.
7. Patients should be able to read, understand and to provide written consent.
8. Voluntarily signed informed consent obtained before any expanded access-related
procedures are performed.
9. Female patients should not be pregnant or plan to become pregnant during participation
and for 6 months after last investigational product administration.
10. Male patients if their sexual partners can become pregnant should use a method of
contraception during participation and for 6 months after the last administration of
the investigated product.
11. Patient is able and willing to comply with the requirements of this Expanded Access.
Exclusion Criteria:
1. Patients with advanced Parkinson's disease. Advanced PD is defined as a significant
disability, wheelchair-bound or bedridden.
2. 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.
3. Patients with medical history of uncontrolled high blood pressure defined as a
deficient standard of care treatment and/or blood pressure > 150/90 mm/Hg during
screening visit.
4. 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.
5. Any of the following abnormal lab findings during screening will disqualify a patient
from this expanded access protocol:
- Hemoglobin (Hgb) <10 G/DL or >18 G/DL
- Hematocrit (HCT) <30% or >55%
- Platelet count < 80 K/UL and or > 450 K/UL.
- White blood cell count WBC < 3.0 K/UL and > 13.0 K/UL.
- Alanine aminotransferase (ALT) of > 75 IU/L
- Aspartate aminotransferase (AST) of > 75 IU/L
- eGFR < 40 mL/min/1.73
- Pre-prandial glucose > 150 MG/DL
- Post-prandial glucose > 200 MG/DL
6. Patients who have received any stem cell treatment in the past six months before 1st
infusion other than stem cells produced by Hope Biosciences.
7. Patients who are unlikely to complete the visits or adhere to the procedures.
8. The patient has previously been diagnosed with a psychiatric disorder, which is
currently uncontrolled.
9. Patients with a history of addiction or dependency or currently abusing or using
substances.
10. Patients with any form of kidney dialysis will be excluded from participation in the
investigation.
11. 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).
12. 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.
13. 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.
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