A Study of TH-SC01 for Treating Complex Perianal Fistula in Perianal Crohn's Disease.

Jinling Hospital, China

Status and phase: Invitation-only; Phase 1

Conditions: Crohn's Disease

Treatments: Drug: TH-SC01

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04939337

20181231

Details and patient eligibility

About

The purpose of this study is to asses the efficacy and Safety of Allogeneic Umbilical Cord-derived Mesenchymal Stem Cells in the Treatment of Complex Perianal Fistula in Perianal Crohn's Disease.

Full description

Crohn´s disease (CD) can affect any part of the digestive system and symptoms of this chronic illness include abdominal pain, bloating, nausea, vomiting and diarrhea. CD also causes bowel wall ulcers, strictures and fistulas (abnormal passages from the intestines to another organ or the skin).

There is an unmet need for effective medical therapy in CD patients with perianal fistulas, not responding to the conventional strategies, including biological therapies. The current study is designed to assess the safety and efficacy of Allogeneic Umbilical Cord-derived Mesenchymal Stem cells from healthy donors for the treatment of perianal fistulas in patients presenting CD.

Primary objective: To assess the safety (incidence of treatment emergent adverse-events) of TH-SC01

Enrollment: 24 estimated patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 1. Signed Informed Consent；
• 2. According to the Diagnostic Criterion for Crohn's Disease in China's 《Consensus on the Diagnosis and Treatment of Inflammatory Bowel Disease》 (2018, Beijing), Crohn's disease was diagnosed at least 6 months before the screening period；
• 3. Crohn's disease activity index (CDAI) score of 220 or less is defined as inactive or mildly active luminal Crohn's disease；
• 4. Through clinical evaluation, MRI evaluation for anal fistula patients；
• 5. Age 18 ~ 70, male or female；
• 6. The serum or urine pregnancy test of a woman of reproductive age must be negative. Both men and women must agree to use a contraceptive method；
• 7. According to the history and related examination, the general health condition is good；
• 8. The eligible patients must at least meet one of the following conditions: patients who have failed to respond to any conventional treatment, such as conventional antibiotic therapy, immunomodulatory drug therapy, anti-tumor necrosis factor (TNF) α monoclonal antibody therapy, and 5-aminosalicylic acid

Exclusion criteria

• 1. CDAI > 220, or due to Crohn's disease activity, treatment needs to be upgraded immediately；
• 2. Patients with abdominal and pelvic abscess or fistula diameter more than 2 cm；
• 3. Patients with rectal and/or anal stenosis and/or active proctitis (due to limited surgical procedures)；
• 4. The number of internal and / or external openings of anal fistula was more than 2 and 3 respectively;
• 5. Patients who received steroid therapy within the first 4 weeks were screened；
• 6. Abnormal laboratory test results： Liver function: total bilirubin ≥1.5 times the upper limit of normal value, aspartate aminotransferase (AST) or alanine aminotransferase (ALT)≥2.5 times the upper limit of normal value; Renal function: Creatinine clearance below 60mL/min or 1.5 times the upper normal limit of serum creatinine (measured value or calculated by the Cockcroft-Gault formula)；
• 7.Patients with malignancy or a history of malignancy, including fistula cancer of any type；
• 8. Patients with severe, progressive, uncontrollable diseases of the liver, blood, gastrointestinal (except Crohn's disease), endocrine, lung, heart, neurological, psychiatric, or brain；
• 9. HIV, syphilis antibody positive, HCV / HBV positive, tuberculosis in the infectious period, etc;
• 10. Patients who are allergic to human serum albumin, human platelet lysates, anesthetic agents or contrast agents；
• 11. Patients with contraindications to MRI scanning；
• 12. Pregnant or lactating women and subjects who cannot commit to using effective contraceptives during the trial and for 6 months after the end of the trial；
• 13. Patients who have undergone major surgery or severe trauma in the past six months；
• 14. Patients who had received any study drug within a certain period of time prior to screening；
• 15.Patients deemed ineligible to participate in this clinical trial by the investigator

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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24 participants in 1 patient group

TH-SC01

Experimental group

Description:

TH-SC01 24 mL suspension of 120 million cells as a perilesional injection, once on Day 0.

Treatment:

Drug: TH-SC01