Intrathecal Administration of Autologous Mesenchymal Stem Cell-derived Neural Progenitors (MSC-NP) in Patients With Multiple Sclerosis

Exclusion Criteria

• •Pregnant or nursing mothers or any woman intending to become pregnant in the next three years
• •All patients will have pre-study liver function tests, PT/PPT, platelets, hematocrit, and renal function laboratory tests done. Only patients whose values are in the normal range as determined by the laboratory norms based on age and sex will be allowed to participate.
• •Use of systemic chemotherapeutic or anti-mitotic medications within three months of study start date due to the possibility of interference with bone marrow procedure
• •Any patients with a history of or with active malignancy
• •Use of steroids within three months of the study start date, as this would suggest a highly active disease state
• •History of cirrhosis due to increased risk of central nervous system (CNS) infection
• •Poorly controlled hypertension because of increased risk for stroke or CNS hemorrhage. Specifically, any patient with a systolic blood pressure value of ≥ 145 mm/Hg or a diastolic blood pressure value of ≥ 95 mm/Hg will be excluded from study participation.
• •History of thyroid disorders or other endocrine disorders because of hormone influence on cell growth
• •History of central nervous system infection or immunodeficiency syndromes due to increased risk of CNS infection
• •Preexisting blood disease (such as bone marrow hypoplasia, leukopenia, thrombocytopenia, or significant anemia) due to invasive nature of bone-marrow aspiration
• •Previous or current history of a coagulation disorder
• •Any metal in the body, which is contraindicated for MRI studies
• •Allergy to any of the antibiotics used in this study, e.g. tobramycin, vancomycin, or gentamicin
• •Patients with alcohol or other substance abuse problems
• •Other major disease that, in the opinion of the Principal Investigator, would preclude participation in the study
• •Patients with HBV, HCV, syphilis, HIV-1, or HIV-2.
• •Any evidence of significant cognitive dysfunction based on a screening history and physical examination because it would preclude giving a truly informed consent
• •Patients who are enrolled in another clinical trial for MS treatment or who have received any study drug/biologics within the last 6 months