Pilot Trial of Mesenchymal Stem Cells for Systemic Lupus Erythematosus

• Status: Completed
• Trial end date: 2018-10-25
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the safety of mesenchymal stromal cells (MSCs) obtained from umbilical cords for the treatment of adults with active systemic lupus erythematosus (SLE).

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Medical University of South Carolina

Criteria

Inclusion Criteria:

• Patients between 18 and 65 years old, male or female, of any race

• Definite SLE by meeting either SLICC or ACR Classification Criteria for SLE

• Evidence of a positive ANA (≥1:80 titer) or positive dsDNA antibody test within 6 months of screening

• Clinically mild to moderately active SLE determined by SLEDAI score ≥4 and ≤10 at screening, despite SOC therapy

• If the patient has BILAG A or two BILAG Bs in the renal organ system, he/she must have completed at least 6 months of therapy with either mycophenolate mofetil or cyclophosphamide for the current episode of nephritis

• Able and willing to give written informed consent

Exclusion Criteria:

• Active CNS lupus affecting mental status

• Active lupus nephritis requiring dialysis

• Laboratory exclusions: eGFR <30, WBC <2.0/mm3, hemoglobin <8 g/dL, platelet count <30,000/mm3, liver enzymes AST or ALT >4 times upper limit normal; Positive testing for HIV, hepatitis B or hepatitis C

• History of malignant neoplasm within the last 3 years, except for adequately treated cancers of the skin (basal or squamous cell) or carcinoma in situ of the uterine cervix

• Pregnant or breast feeding; males or females not willing to use adequate contraception

• History of renal transplantation

• Herpes zoster within the past 90 days or any infection requiring hospitalization or intravenous antibiotics within the past 60 days

• Clinically significant EKG or chest X-ray abnormalities

• Any other medical condition, related or unrelated to SLE, that in the opinion of the investigator would render the patient inappropriate or too unstable to complete study protocol

• Use of prednisone >0.5 mg/kg/day (or equivalent corticosteroid) within 1 month of Baseline visit

• Change or addition to immunosuppressant regimen within 3 months of Baseline visit (except corticosteroids); Use of other experimental therapeutic agents within 3 months of Baseline visit

• Having received belimumab within 3 months of Baseline, or having received rituximab or other B cell depleting biologic therapy within 6 months of Baseline.

• Comorbidities requiring corticosteroid therapy

• Current substance abuse or recent (within 60 days) history of substance abuse