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CompletedNCT03449069Updated Mar 13, 2024

Pediatric MSC-AFP Sub-study for Crohn's Fistula

A Phase 1 interventional study of MSC-AFP in Fistula in Ano and Crohn Disease, sponsored by Mayo Clinic. Completed at 1 site in United States. Open to participants aged 12 Years to 17 Years. Per ClinicalTrials.gov, last updated 2024-03-13.

Sponsored by Mayo Clinic · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
1
Allocation
Not applicable
Ages
12 Years to 17 Years
Sex
All
01

Study summary

The purpose of this study is to determine the safety of using an autologous mesenchymal stromal cell (MSC) coated fistula plug in people with fistulizing Crohn's disease. Autologous means these cells to coat the plug come from the patient.

Read the detailed description

The investigators propose to study the safety of autologous mesenchymal stromal cell transfer using a biomatrix (the Gore Bio-A Fistula Plug) in a Phase I study using a single dose of 20 million cells. 5 patients (age 12 to 17 years) with Crohn's perianal fistulas will be enrolled.

Subjects will undergo standard adjuvant therapy including drainage of infection and placement of a draining seton. Six weeks post placement of the draining seton, the seton will be replaced with the MSC loaded Gore fistula plug as per current clinical practice. The subjects will be subsequently followed for fistula response and closure for 24 months. This is an autologous product derived from the patient and used only for the same patient.

02

Conditions studied

  • Fistula in Ano
  • Crohn Disease
03

Who can participate

Ages eligible
12 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Males and females 12-17 years of age.
  2. Residents of the United States.
  3. Crohn's disease with single or multiple draining complex perianal fistulae (definition as below) for at least three months despite standard therapy (definition below).
  4. Concurrent therapies with corticosteroids, 5-aminosalicylate (5-ASA) drugs, thiopurines, methotrexate (MTX), antibiotics, and anti-tumor necrosis factor (TNF) therapy are permitted.
  5. All patients should have undergone a colonoscopy in last 12 months to rule out malignant or premalignant condition
  6. Have no contraindications to MR evaluations: e.g. pacemaker or magnetically active metal fragments, claustrophobia
  7. Ability to comply with protocol
  8. Competent and able to provide written informed consent (and assent where appropriate).
  9. Must have failed standard medical therapy including anti-TNF agents

Exclusion criteria

Exclusion Criteria

  1. Inability to obtain informed consent (and assent where appropriate).
  2. Clinically significant medical conditions within the six months before administration of MSCs: e.g. sepsis, pneumonia active serious infection or other conditions that would, in the opinion of the investigators, compromise the safety of the patient.
  3. Specific exclusions;

    a. Evidence of hepatitis B, C, or HIV

  4. History of cancer including melanoma (with the exception of localized skin cancers)
  5. Investigational drug within thirty (30) days of baseline
  6. A resident outside the United States
  7. Pregnant or trying to become pregnant, or breast feeding.
  8. History of clinically significant auto-immunity (other than Crohn's disease) or any previous example of fat-directed autoimmunity
  9. Previous allergic reaction to a perianal fistula plug.
  10. If adipose tissue is not technically feasible
  11. Weight less than 35 kg
  12. Allergic to local anesthetics
  13. Non-enterocutaneous tracts (i.e. recto-vaginal, entero-vesicular)
04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
1 participant (actual)

Study arms

  • Experimental
    MSC-AFP

    This is a single treatment group study. All patients will receive treatment of a stem cell coated fistula plug.

    Drug: MSC-AFP

Interventions

  • DrugMSC-AFP

    Patients will have a mesenchymal stromal cell coated anal fistula plug placed in their Crohn's perianal fistula tract.

    Also known as: mesenchymal stromal cell coated anal fistula plug

05

What researchers measure

Primary outcomes

  1. Number of participants with treatment-related adverse events (safety and toxicity)

    Participants will have a health assessment and blood work done at each study visit to monitor for adverse events.

    Time frame: 2 months to approximately at 24 months

Secondary outcomes

  1. Number of participants with response to the treatment regarding cessation of drainage from the treated fistula.

    Participants will have a clinical assessment of fistula drainage at each study visit.

    Time frame: 2 months to approximately at 24 months

  2. Number of participants with radiographic response to the treatment regarding the treated fistula.

    Participants will have an assessment of healing radiographically by magnetic resonance imaging (MRI) at Week 2 visit, Week 8, and Week 24.

    Time frame: Week 2, Week 8, and Week 24

06

Study locations

1 site
  • Mayo Clinic in Rochester
    Rochester, Minnesota 55905, United States
07

References and documents

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT03449069
Lead sponsor
Mayo Clinic
Responsible party
Michael C. Stephens (Sponsor-Investigator, Mayo Clinic) — Principal investigator
First posted
Feb 28, 2018
Start date
Jul 23, 2018
Primary completion
Dec 31, 2023
Completion
Dec 31, 2023
Last update
Mar 13, 2024

Study contacts

Michael C Stephens
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.

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