Title
The Evaluation of the Effect of Mesenchymal Stem Cells on the Immune System of Patients With ALS
The Evaluation of the Effect of Wharton's Jelly Mesenchymal Stem Cells (WJMSCs) on the Immune System of Patients With Amyotrophic Lateral Sclerosis (ALS)
Phase
Phase 1/Phase 2Lead Sponsor
Polski Bank Komorek Macierzystych JSC (PBKM)Study Type
InterventionalStatus
Active, not recruitingIndication/Condition
Amyotrophic Lateral SclerosisIntervention/Treatment
Mesenchymal stem cells isolated from Wharton's jellyStudy Participants
20The objective of this study is to evaluate the safety of intrathecal administration of Wharton's Jelly Mesenchymal Stem Cells (WJMSC) and the impact on the immune system of patients with Amyotrophic Lateral Sclerosis.
Clinical Phase: I/II
Population: Patients with Amyotrophic Lateral Sclerosis.
Project Design: One arm, non-blinded, open label study
Planned Sample Size: 20 patients
Investigational Medicinal Product: active IMP - mesenchymal stem cells isolated from Wharton's jelly
Screening:
Three visits on site to check the eligibility criteria (around 90, 60 and 30 days before first IMP administration)
Treatment (IMP administration):
Each patient will receive IMP three times: on baseline (day 0), 30 and 60 days after baseline (+/- 7 days).
Administration route: intrathecal
Follow up:
Duration: 18 months after first IMP administration Four on-site visits (3, 6, 9, 12 months after first IMP administration) and seven phone visits (4, 5, 7, 8, 10, 11 and 18 months after first IMP administration)
Intrathecal administration of mesenchymal stem cells
It is planned that IMP administration will be performed three times for each enrolled patient. IMP administration could be performed only if the patients does not have any contraindications for lumbar puncture.
Inclusion Criteria: Adult patients (at least 18 years old) The minimum patient's weight is not less than 40 kg Diagnosis of sporadic ALS, definite or probable, as defined by El Escorial World Federation of Neurology criteria History of ALS symptoms less than 2 years duration from the first symptoms of the disease More than 6 months from diagnosis of the disease Disease progression at 6 past months at least 3 points during this period of time assessed in ALSFRS-R scale ALSFRS-R scale of at least 30 at screening appointment Forced vital capacity >70% of predicted value for age, gender and height Treatment with stable dose of riluzole(2x 50mg per 24h) before baseline visit (for at least 1 month) Capable of providing written informed consent Able to comply with study requirements and willing to follow all study procedures and follow-up visits Women of child-bearing age and men with partners of child-bearing potential must agree to use two forms of contraceptive therapy throughout the course of the trial Women of child-bearing age must undergo pregnancy test Polish-language native speakers or patients who are proficient in the Polish language Exclusion Criteria: Pregnancy or breastfeeding Tracheostomy Ventilator dependence Renal disease with creatinine >2mg/dl Liver disease with ALT, AST or GGTP 2-fold higher than upper normal limit Positive test for HBV, HCV, HIV with NAT method Positive tests for syphilis Any other clinically significant abnormalities on laboratory evaluation Any condition that would compromise ability of undergoing lumbar puncture Active systemic disease Autoimmune disease (Hashimoto disease under control is allowed) Uncontrolled diabetes (HbA1c > 8%) Pulmonary disease that could affect interpretation of spirometry Neurological concomitant disease Unstable psychiatric concomitant disease High risk of suicide History of substance abuse within past year History of malignancy, within the previous 5 years, including melanoma with exception of localized skin cancers Any other clinically significant medical condition that can compromise patient's safety in the opinion of the investigator Treatment with immunomodulatory drugs (for example immunoglobulins, corticosteroids or other immunosuppressant) in last 6 months Participation in another clinical trial in last 6 months Previous cellular therapy of any kind Hypersensitivity to any component used in the cell culture Nuchal rigidity and other signs of meningitis Patients on chronic anticoagulation treatment (heparin/ warfarin/acenocoumarol/(N)OAC)
