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DB-3Q bmMSC-EVs in Patients With Perianal Fistulizing Crohn's Disease

NCT06918808 · Direct Biologics, LLC
In plain English

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Official title
A Phase 2a Study of Allogeneic Bone Marrow Mesenchymal Stem Cell Derived Extracellular Vesicle Isolate Product (DB-3Q) in Patients With Perianal Fistulizing Crohn's Disease
About this study
This is a double-blind, randomized, placebo-controlled, sequential cohort, ascending dose clinical trial to evaluate the safety and determine the efficacy of ascending doses of DB-3Q for the treatment of Perianal Fistulizing Crohn's Disease.
Eligibility criteria
Inclusion Criteria: 1. Written informed consent from participant 2. Men and women 18-75 years of age with a diagnosis of Crohn's Disease for at least six months duration prior to Day 1 3. Single and/or multi-tract perianal fistula(s) with 2 or fewer openings, that are actively draining 4. Failed at least one medical therapy within the last year including, but not limited to, antibiotics, immunomodulators (6-MP, methotrexate, azathioprine), monoclonal antibodies (adalimumab, certolizumab, golimumab, guselkumab, infliximab, risankizumab, ustekinumab, vedolizumab), or small molecule inhibitors (tofacitinib, upadacitinib) 5. Previous failed surgical intervention, including seton placement at least two weeks prior to screening, or are not candidates for surgical intervention or are not willing to undergo surgical intervention for the management of their fistula 6. Medical therapy for CD stable for at least 2 months prior to Day 1 (Changes in dosing or dosing intervals related to serum drug levels are not permitted) Exclusion Criteria: 1. Lack of informed consent 2. Pregnant woman, woman of childbearing potential without a documented negative urine or serum pregnancy test, or woman who is breast feeding 3. A participant who is unwilling to use medically acceptable contraception methods during participation in study 4. Active perianal abscess or infection at screening or Day 1 5. Clinically significant medical conditions within six months before Day 1 that would, in the opinion of the Investigator, compromise the safety of the participant 6. Confirmed HIV, Hepatitis B, or Hepatitis C infections 7. History of cancer including melanoma (with the exception of localized non-melanoma skin cancers) within one year of screening 8. History of colorectal cancer within 2 years of screening 9. Use of investigational therapy or treatment within 30 days prior to Day 1
Study design
Enrollment target: 36 participants
Allocation: randomized
Masking: quadruple
Age groups: adult, older_adult
Timeline
Starts: 2025-05-19
Estimated completion: 2026-10-31
Last updated: 2026-02-23
Interventions
Biological: DB-3QBiological: Placebo
Primary outcomes
  • Combined Remission (24 Weeks)
Sponsor
Direct Biologics, LLC · industry
Contacts & investigators
ContactExecutive Vice President, Clinical Affairs, MS · contact · clinicalaffairs@directbiologics.com · 1-800-791-1021
All locations (3)
Direct Biologics Investigational SiteRecruiting
Aurora, Colorado, United States
Direct Biologics Investigational SiteRecruiting
St Louis, Missouri, United States
Columbia University Irving Medical Center/NYPHRecruiting
New York, New York, United States
DB-3Q bmMSC-EVs in Patients With Perianal Fistulizing Crohn's Disease · TrialPath