Phase 2 Trial of Mesenchymal Stem Cells in Systemic Lupus Erythematosus (MiSLE)

Systemic Lupus Erythematosus Clinical Trial

Official title:

A Phase II Controlled Trial of Allogeneic Mesenchymal Stem Cells for the Treatment of Refractory Lupus

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02633163
• Other study ID #: MUSC-UCMSC-001
• Status: Recruiting
• Phase: Phase 2
• Start date: October 26, 2018
• Est. completion date: June 2025

Study information

• Verified date: February 2024
• Source: Medical University of South Carolina
• Contact: Gary Gilkeson
• Phone: (843) 792 - 6043
• Email: gilkeson[@]musc.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of mesenchymal stem cells (MSCs) obtained from umbilical cords for the treatment of adults with systemic lupus erythematosus (SLE). The goal of this study is to determine if patients receiving an MSC infusion plus standard of care respond better than patients receiving placebo infusion plus standard of care.

Description:

A phase 2 multicenter (several medical research centers participating), placebo controlled, randomized (assigned by chance), double blind (neither the participant nor the investigator will know if active drug or placebo is assigned) trial to evaluate the safety and efficacy of mesenchymal stem cells (MSCs) for the treatment of systemic lupus erythematosus (SLE) in adults.

The MSCs will be obtained from healthy donor umbilical cords and two doses of MSCs will be tested. The cells will be produced at the Medical University of South Carolina (MUSC) and will be shipped to other participating centers for patients with SLE. Participants will receive either active drug or placebo through a single IV infusion. All participants will receive standard of care and their safety will be monitored throughout the study.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 81
• Est. completion date: June 2025
• Est. primary completion date: December 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

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

• Historical presence of at least 4 of 11 of the ACR Classification Criteria

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

• Clinically active SLE determined by SLEDAI score =6 and the presence of at least one BILAG A or BILAG B at screening, despite standard-of-care therapy

• If the patient has a BILAG A or BILAG B score in the renal organ system, he/she must have completed at least 6 months of therapy for the current episode of nephritis prior to Screening. Therapy must include at least 6 months of mycophenolate or at least 3 months of cyclophosphamide followed by mycophenolate or azathioprine

• 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, tuberculosis (TB), or chest X-ray (CXR) findings consistent with TB or latent fungal infection.

• History of malignant neoplasm within the last 5 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

• A woman of childbearing potential (not post-menopausal or surgically sterile) who is not willing to use adequate contraception

• History of renal transplantation

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

• Clinically significant EKG or chest X-ray changes

• 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 2 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 one year) history of substance abuse

Related Conditions & MeSH terms

• Lupus Erythematosus, Systemic
• Systemic Lupus Erythematosus

Intervention

Drug:
• Low Dose Mesenchymal Stem Cells (MSCs)
Participants will receive a single IV infusion of Mesenchymal Stem Cells (MSCs) 1 x 10^6 cells/kg in Plasma-Lyte A solution. All participants will receive the infusion at the Baseline (Day 0) visit. All participants will continue on their standard-of-care therapy during the trial.
• High Dose Mesenchymal Stem Cells (MSCs)
Participants will receive a single IV infusion of Mesenchymal Stem Cells MSCs 5 x 10^6 cells/kg in Plasma-Lyte A solution.
• Placebo Infusion
Participants will receive a placebo infusion that does not contain any mesenchymal stem cells.The placebo infusion will consist of Plasma-Lyte A, which is the same vehicle used to deliver the MSCs in the experimental groups.

Locations

Country	Name	City	State
United States	Emory University	Atlanta	Georgia
United States	University of North Carolina at Chapel Hill	Chapel Hill	North Carolina
United States	Medical University of South Carolina	Charleston	South Carolina
United States	Northwestern University	Chicago	Illinois
United States	Cedars-Sinai Medical Center	Los Angeles	California
United States	The Feinstein Institute for Medical Research	Manhasset	New York
United States	Oklahoma Medical Research Foundation	Oklahoma City	Oklahoma
United States	University of Rochester Medical Center	Rochester	New York
United States	University of California - San Diego	San Diego	California

Sponsors (1)

Lead Sponsor	Collaborator
Medical University of South Carolina

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical response at Week 24 as defined by the SLE Responder Index (SRI):	Systemic Lupus Erythematosus Responder Index (SRI) is defined as a greater than or equal to (=) 4 point reduction in the Systemic Lupus Erythematosus Disease Activity Index score (SLEDAI), no new British Isles Lupus Assessment Group (BILAG) A or no more than 1 new BILAG B domain score, and no deterioration from Baseline in the Physician's Global Assessment (PGA) by greater than or equal to (=) 0.3 points.; Additionally, to be a "responder", corticosteroid dose must be less than of equal to (=)10 mg/day of prednisone or equivalent by the Week 20 visit and be maintained at less than or equal to 10 mg/day through Week 24.	Week 24
Secondary	Change in SLEDAI score between groups	Changes in Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) between the experimental and placebo group.	Baseline to Weeks 12, 24, and 52
Secondary	Renal and non-renal organ system flares	Frequency of renal and non-renal organ system flares at or before Weeks 12, 24, and 52, defined by the BILAG criteria.	At or before Weeks 12, 24, and 52
Secondary	Changes in SLICC-DI	• Change in SLICC-DI from Baseline to Week 52 to assess for accumulation of new damage (SLE-related or treatment-related)	Baseline to Week 52
Secondary	Changes in HR-QOL	Changes in HR-QOL (measured by SF36 v2) from Baseline to Weeks 12, 24, and 52	Baseline to Week 52
Secondary	Changes in Fatigue	Changes in fatigue (measured by PROMIS Fatigue Short Form (SF)) from Baseline to Weeks 12, 24, and 52	Baseline to Week 52
Secondary	Changes in Pain	Changes in pain (measured by PROMIS Pain SF) from Baseline to Weeks 12, 24, and 52	Baseline to Week 52
Secondary	Changes in Depression	Changes in depression (measured by PROMIS Depression SF) from Baseline to Weeks 12, 24, and 52	Baseline to Week 52
Secondary	Changes in patient-reported lupus-specific disease status	Changes in patient-reported lupus-specific disease status (measured by the LupusPro and LIT) from Baseline to Weeks 12, 24, and 52	Baseline to Week 52
Secondary	Steroid-sparing effect	Steroid-sparing effect (measured by discontinuation of corticosteroids and time to discontinuation among those taking corticosteroids)	Baseline to Week 52
Secondary	Cumulative systemic steroid dose	Cumulative systemic steroid dose (PO, IV, IM) at Week 52	Week 52
Secondary	Changes in the presence of serum and urine biomarkers of SLE activity:	Changes in the presence of serum and urine biomarkers of SLE activity: SLE-related cytopenias, low serum complement levels, anti-dsDNA levels or urine protein measures from Baseline to Weeks 12, 24, and 52.	Baseline to Week 52