Re-treatment From a Phase I Study of MSC-AFP in Patients With Perianal Fistulas

Last updated: December 31, 2019
Sponsor: William A. Faubion, M.D.
Overall Status: Completed

Phase

1

Condition

Acne Inversa

Rectal Disorders

Treatment

N/A

Clinical Study ID

NCT03209700
17-004503
  • Ages 18-65
  • All Genders

Study Summary

This study is an extension to re-treat partial and non-responders from the previously approved Phase 1 MCS-AFP protocols IRB #12-009716 (Crohn's Disease perianal fistulas) and 15-003200 (cryptoglandular perianal fistulas).

Eligibility Criteria

Inclusion

Inclusion Criteria

  1. Males and females 18-65 years of age.

  2. Residents of the United States.

  3. Single draining perianal fistula for at least three months despite standard therapy

  4. Concurrent therapies are permitted (such as antibiotics, corticosteroids, thiopurines).

  5. Have no contraindications to MR evaluations: e.g. pacemaker or magnetically active metal fragments, claustrophobia

  6. Ability to comply with protocol

  7. Competent and able to provide written informed consent

  8. Patients that were treated with an MSC-coated fistula plug in the study IRB#12-009716 or IRB#15-003200

Exclusion Criteria

  1. Inability to give informed consent.

  2. Clinically significant medical conditions within the six months before administration of MSCs: e.g. myocardial infarction, active angina, congestive heart failure or other conditions that would, in the opinion of the investigators, compromise the safety of the patient.

  3. Specific exclusions: 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. Previous allergic reaction to a perianal fistula plug.

  8. Allergic to local anesthetics

  9. Pregnant patients or trying to become pregnant or breast feeding.

  10. Non-enterocutaneous tracts (i.e. recto-vaginal, entero-vesicular)

Study Design

Total Participants: 7
Study Start date:
July 20, 2017
Estimated Completion Date:
December 10, 2019

Study Description

This study is an extension to re-treat partial and non-responders from the previously approved Phase 1 MCS-AFP protocols IRB #12-009716 (Crohn's Disease perianal fistulas) and 15-003200 (cryptoglandular perianal fistulas). This study will enroll patients that have persistent symptomatic perianal disease despite being treated with an MSC coated fistula plug, and also treat patients that have had recurrence of their perianal fistula.

As per the previously approval treatment under IND 15356, patients will have a single affected fistula treated, which is the same fistula that was treated in the original protocol. The matrix for delivering the cells is a Gore Bio-A Fistula Plug.

Subjects will be screened at outpatient clinic visits and interested qualified subjects will be offered participation in the trial and consented. At the first study visit (Visit 1; Screening visit), the patient will be evaluated and assessment will be made if an EUA is clinically necessary to assess the fistula. As this is a re-treatment trial, patients with incomplete response to initial plug placement typically have close follow up, recent MRI imaging, and may have a seton in place. If an EUA is clinically indicated, this would be by a colorectal surgeon for drainage of sepsis and placement of a seton as part of the standard clinical care for perianal fistula.

Patients will return on: Day 1, Week 4, Week 12, and Week 24.

Connect with a study center

  • Mayo Clinic in Minnesota

    Rochester, Minnesota 55905
    United States

    Site Not Available

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