Perianal Fistula Clinical Trial
Official title:
A Phase I Study of Autologous Mesenchymal Stromal Cell Coated Fistula Plug in Patients With Fistulizing Crohn's Disease: Pediatric Sub-study
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. 20 patients (age 12 to 17 years) with Crohns 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.
Visit 1: Patients will be evaluated for eligibility (inclusion/exclusion checklist) and
written, informed consent will be obtained. Patients will undergo general exam with vital
signs. Patients will be scheduled for a fat biopsy to collect the tissue needed to grow MSC.
In the event there is no cell growth from the tissue obtained from the first biopsy, one
further attempt will made from a second tissue sample from this patient. However, if the
second attempt fails to grow cells, no further attempts will be made, and the subject will
not continue in the study.
The subjects will be subsequently followed for fistula response and closure for 24 months.
Study visits are Day 1, Week 2, Week 4, Week 8, Week 12, Week 24, Week 52, and Week 104. This
is an autologous product derived from the patient and used only for the same patient.
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