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Clinical Trials/NCT01314092
NCT01314092
Terminated
Phase 2

Phase II Study to Evaluate Efficacy and Safety of ANTG-ASC (Autologous Cultured Adipose-derived Stem Cells) on the Complex Fistula Patients

Anterogen Co., Ltd.6 sites in 1 country15 target enrollmentJanuary 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Complex Perianal Fistula
Sponsor
Anterogen Co., Ltd.
Enrollment
15
Locations
6
Primary Endpoint
Number of patients with complete closure of fistula (week 8)
Status
Terminated
Last Updated
9 years ago

Overview

Brief Summary

Mesenchymal stem cells derived from adipose tissue are pluripotent to differentiate into myocytes, adipocytes or others. They have an immunosuppressive activity. Complex perianal fistula is difficult to cure and easy to relapse. Autologous adipose stem cells have shown efficacy and safety on Crohn's fistula in phase 1 study. Based on these results, the investigators would apply autologous adipose stem cells on complex perianal fistula to evaluate their efficacy and safety.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
September 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Anterogen Co., Ltd.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • a patient who has complex perianal fistula
  • a patient who is negative in pregnancy test
  • a patient who has submitted a written consent

Exclusion Criteria

  • a patient who has participated in other clinical studies within 30 days before this clinical trial or has not passed 5 fold period of a half-life of other investigational drugs.
  • a patient who has a history of variant Creutzfeldt Jacobs disease or related diseases
  • a patient who is allergic to anesthetics, bovine derived proteins or a fibrin glue
  • a patient who has an autoimmune disease
  • a patient who has infectious diseases such as hepatitis B virus (HBV), hepatitis C virus (HCV) or human immunodeficiency virus (HIV)
  • a patient who has sepsis or active tuberculosis
  • a patient who is pregnant or breast feeding
  • a patient who has inflammatory Bowel disease
  • over 2cm in diameter of fistula

Outcomes

Primary Outcomes

Number of patients with complete closure of fistula (week 8)

Time Frame: 8 weeks

Proportion of patients with completely closed fistula (week 8)

Secondary Outcomes

  • Grade of investigator's satisfaction(8 weeks)
  • Number of patients with closed fistula(8 weeks)
  • Photo of target fistula(8 weeks)
  • Number of patients with adverse events(8 weeks)

Study Sites (6)

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