A Phase 1 interventional study of MSC-AFP in Perianal Crohn's Disease, sponsored by William A. Faubion, M.D.. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2020-01-03.
Sponsored by William A. Faubion, M.D. · Phase 1, Interventional, and Treatment
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. Twenty adult patients (age 18 years or older) with refractory, complicated perianal fistulizing Crohn's disease will be enrolled. Subjects will undergo standard adjuvant therapy including drainage of infection and placement of a draining seton with continuation of pre-existing anti-Crohn's therapy. Six weeks post placement of the draining seton, the seton will be replaced with the MSC loaded Gore® Bio-A® 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.
1,880 studies on the registry are indexed under Crohn Disease; 462 are open to participants now.
This study's enrollment of 20 is below the median of 66 across 1,188 interventional studies indexed under Crohn Disease.
Browse Crohn Disease studies →William A. Faubion, M.D. is the lead sponsor of 4 studies on the registry; none are open to participants now.
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Exclusion Criteria
Only 1 arm: treatment with MSC-AFP
Drug: MSC-AFP
To determine the safety and toxicity of using autologous MSC coated fistula plug in patients with fistulizing Crohn's Disease.
The primary endpoint of this study is to determine the safety and feasibility of using adipose derived, autologous mesenchymal stromal cells (MSC) bound to the Gore® Bio-A® Fistula Plug for treatment of refractory CD perianal fistulae.
Time frame: 2-24 months
To assess in preliminary fashion the response of fistula healing induced by the GORE plug containing MSC
To assess in preliminary fashion the response of fistula healing induced by the GORE plug containing MSC i) Clinically by drainage assessment and ii) Radiographically by MRI, the gold standard test for assessment of healing.
Time frame: 2-24 months
This study is completed, as verified in Dec 2019. You cannot join it, but the record below documents what was studied.
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William A. Faubion, M.D.