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Clinical Trials/NCT02150551
NCT02150551
Completed
Phase 1

Safety and Tolerability Of Allogeneic Mesenchymal Stromal Cells in Pediatric Inflammatory Bowel Disease

Catherine Bollard1 site in 1 country1 target enrollmentJune 7, 2018

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Inflammatory Bowel Diseases
Sponsor
Catherine Bollard
Enrollment
1
Locations
1
Primary Endpoint
Number of Subjects Who Experience Serious Adverse Events, Adverse Events, and/or Early Treatment Discontinuations.
Status
Completed
Last Updated
last year

Overview

Brief Summary

In this trial, investigators will infuse donor bone marrow mesenchymal stromal cells intravenously, as a treatment for pediatric Crohn's disease or ulcerative colitis that has not responded to conventional therapies. The goals of this study are to test the safety and tolerability of donor mesenchymal stromal cells in children with Inflammatory Bowel Disease.

Mesenchymal stromal cells support the development of blood cells within the bone marrow. When isolated from a donor and infused into an animal or human, they have been demonstrated to travel to areas of inflammation, to alter immune responses, to decrease pro-inflammatory cytokines, and to promote tissue repair. Infusion of these cells does not lead to rejection. These properties lead investigators to hypothesize that that these may be they may be beneficial in treating inflammatory bowel disease.

Detailed Description

In this trial, investigators will infuse donor bone marrow mesenchymal stromal cells intravenously, as a treatment for pediatric Crohn's disease or ulcerative colitis that has not responded to conventional therapies. Mesenchymal stromal cells support the development of blood cells within the bone marrow. They have also been demonstrated to travel to areas of inflammation, to alter immune responses, to decrease pro-inflammatory cytokines, and to promote tissue repair. Infusion of these cells does not lead to rejection. These properties lead investigators to hypothesize that that these may be they may be beneficial in treating inflammatory bowel disease. Investigators will culture donated bone marrow mesenchymal stromal cells in a unique automated system, and infuse the cells in a fresh, replicating stage of growth. This study is to test the safety and tolerability of donor mesenchymal stromal cells in children with Inflammatory Bowel Disease.

Registry
clinicaltrials.gov
Start Date
June 7, 2018
End Date
September 5, 2018
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Catherine Bollard

Director- Center for Emerging Technologies in Immune Cell Therapies (CETI)

Children's National Research Institute

Eligibility Criteria

Inclusion Criteria

  • For the young adult cohort, patients must be ages 17 ≤22 years
  • For the pediatric cohort, patients must be ages 12 ≤16 years
  • Patients must have moderate-severely active CD or UC (defined in section 2.3), and documented active disease on flexible sigmoidoscopy, colonoscopy or MR enterography within the preceding 2 months.
  • Patients who have failed or are intolerant of biologic therapy. Specifically, the patient will have recurrence or persistence of active disease despite current or past treatment with a biologic. At the time of enrollment, study subjects may be currently receiving 5-aminosalicylates, corticosteroids (≤ 20 mg daily or up to 0.5 mg/kg/day if weight \<40 kg), methotrexate, 6MP/azathioprine, or a biologic (either as monotherapy or in combination). During the treatment phase, if the treating physician thinks that a medication dose should be lowered to avoid side effects, this should be recorded.
  • Patient or parent/guardian capable of providing informed consent.

Exclusion Criteria

  • • Patients \< 12 years of age or \>22 years of age
  • Pregnant or breastfeeding. Serum pregnancy test must be negative at screening for female subjects of childbearing potential. Urine pregnancy test must remain negative at each of 4 infusion visits.
  • Patients with toxic mega-colon or intestinal perforation
  • Evidence of autoimmune chronic active hepatitis or sclerosing cholangitis.
  • Patients with fever \> 39° C or clinically significant active infection within 1 week (i.e. chronic infections including Hepatitis B/C or HIV or acute infections, including urinary tract infection and respiratory tract infection)
  • Received an agent not approved by the FDA for marketed use in any indication or any small molecule inhibitors (i.e. naltrexone) within 60 days of enrollment.
  • Subjects who are taking greater than 20 mg (or if body weight \<40 kg, 0.5 mg/kg) of prednisone daily.
  • Clinically significant abnormal biochemical and hematological parameters, including:
  • Neutrophil count \< 1000 cells/mm3
  • Hemoglobin \< 8 g/dl

Outcomes

Primary Outcomes

Number of Subjects Who Experience Serious Adverse Events, Adverse Events, and/or Early Treatment Discontinuations.

Time Frame: 45 days after the last infusion

Safety and tolerability of the administration of human allogeneic bone marrow-derived stromal cells to children and young adults with IBD, measured by the frequency of any SAEs, AEs and/or early treatment discontinuations. Weekly infusions for 8 weeks, post-treatment assessment 45 days after last infusion, three additional follow-up visits over 2 years.

Secondary Outcomes

  • Proportion of Patients With Clinical Response(45 days after last infusion)
  • Number of Subjects Demonstrating an Improvement of Laboratory Tests Reflecting Systemic Inflammation.(45 days after last infusion)

Study Sites (1)

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