Expanded Access Protocol: Repeated Administration of Nurown® (Autologous MSC-NTF Cells) for the Treatment of ALS
NCT ID: NCT04681118
Last Updated: 2024-04-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NO_LONGER_AVAILABLE
EXPANDED_ACCESS
Brief Summary
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Detailed Description
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The participants will undergo up to three intrathecal (IT) treatments with NurOwn® (MSC-NTF cells).
In the first treatment period, the participant received up to three intrathecal (IT) treatments with NurOwn® (MSC-NTF cells) at T1, T2 and T3 and was followed for 12 weeks after the third treatment.
In the second treatment period, the participant will receive up to three intrathecal (IT) treatments with NurOwn® (MSC-NTF cells) every 8 weeks at T4, T5 and T6.
Following the last EAP treatment, the participant will be followed for three additional monthly visits (in-person, if feasible, or by telephone call or telemedicine in consideration of the ongoing COVID-19 pandemic) through the final protocol visit, during which the ALSFRS-R and safety assessments will be collected
Conditions
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Interventions
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NurOwn (MSC-NTF cells)
Intrathecal administration
Eligibility Criteria
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Inclusion Criteria
2 Able to provide to the Investigator written informed consent regarding the investigational drug, or, as applicable, on whose behalf a legally authorized representative of the participant has provided such consent.
3\. Able to safely undergo all study procedures.
Exclusion Criteria
2. History of clinically significant autoimmune disease (excluding thyroid disease) myelodysplastic or myeloproliferative disorder, leukemia or lymphoma, whole body irradiation, hip fracture, or severe scoliosis.
3. Any unstable clinically significant medical condition other than ALS (e.g., within six months of baseline, had myocardial infarction, angina pectoris, and/or congestive heart failure), treatment with anticoagulants that, in the opinion of the Investigator, would compromise the safety of the participant.
4. Any history of malignancy within the previous 5 years, with the exception of non- melanoma localized skin cancers (with no evidence of metastasis, significant invasion, or re-occurrence within three years of baseline).
5. Current use of immunosuppressant medication or use of such medication within 4 weeks of the pre-treatment visit.
6. Any history of acquired or inherited immune deficiency syndrome.
7. Tracheostomy and/or mechanical ventilation. Feeding tube use, BiPAP or NIV are not exclusionary.
8. Pregnant women or women currently breastfeeding or unwilling to use effective birth control methods during the treatment (if of childbearing age).
9. Positive test result for Hepatitis B virus (HBV; surface antigen (HBsAg) and IgM antibodies to core antigen (IgM anti-HBc)), Hepatitis C virus (HCV), Human Immune deficiency virus (HIV) 1 and 2.
18 Years
63 Years
ALL
No
Sponsors
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Brainstorm-Cell Therapeutics
INDUSTRY
Responsible Party
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Locations
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University of California Irvine Alpha Stem Cell Clinic
Irvine, California, United States
California Pacific Medical Center
San Francisco, California, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
UMass Medical School
Worcester, Massachusetts, United States
Mayo Clinic
Rochester, Minnesota, United States
Countries
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Other Identifiers
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BCT-003-US
Identifier Type: -
Identifier Source: org_study_id
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