Study to Assess the Safety and Efficacy of Allogeneic Umbilical Cord-derived Mesenchymal Stem Cells(TH-SC01), for Treatment of Complex Perianal Fistulas in Perianal Crohn's Disease.
试验速览
- 阶段
- 1 期
- 发起方
- 入组人数
- 24
- 试验地点
- 1
- 主要终点
- Percentage of Participants who Achieve Combined Remission
研究概览
简要总结
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.
详细描述
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
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Signed Informed Consent；
- •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；
- •Crohn's disease activity index (CDAI) score of 220 or less is defined as inactive or mildly active luminal Crohn's disease；
- •Through clinical evaluation, MRI evaluation for anal fistula patients；
- •Age 18 ~ 70, male or female；
- •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；
- •According to the history and related examination, the general health condition is good；
- •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
排除标准
- •CDAI > 220, or due to Crohn's disease activity, treatment needs to be upgraded immediately；
- •Patients with abdominal and pelvic abscess or fistula diameter more than 2 cm；
- •Patients with rectal and/or anal stenosis and/or active proctitis (due to limited surgical procedures)；
- •The number of internal and / or external openings of anal fistula was more than 2 and 3 respectively;
- •Patients who received steroid therapy within the first 4 weeks were screened；
- •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；
- •Patients with severe, progressive, uncontrollable diseases of the liver, blood, gastrointestinal (except Crohn's disease), endocrine, lung, heart, neurological, psychiatric, or brain；
- •HIV, syphilis antibody positive, HCV / HBV positive, tuberculosis in the infectious period, etc;
- •Patients who are allergic to human serum albumin, human platelet lysates, anesthetic agents or contrast agents；
- •Patients with contraindications to MRI scanning；
- •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；
- •Patients who have undergone major surgery or severe trauma in the past six months；
- •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
研究组 & 干预措施
TH-SC01
TH-SC01 24 mL suspension of 120 million cells as a perilesional injection, once on Day 0.
干预措施: TH-SC01 (Drug)
结局指标
主要结局
Percentage of Participants who Achieve Combined Remission
时间窗: 24 weeks
Combined remission is defined as the closure of all treated external openings that were draining at baseline despite gentle finger compression, and absence of abscess(es) \>2 cm (in at least 2 dimensions) of the treated perianal fistula(s) confirmed by central magnetic resonance imaging (MRI) assessment or transrectal ultrasonography(TRUS)
次要结局
- Percentage of Participants who Achieve Clinical Response(Up to Week 24)
- Percentage of Participants who Achieve Clinical Remission(Up to Week 24)
- Percentage of Participants who decrease in PDAI(0、4、8、16、24 weeks)
- Percentage of Participants who decrease in IBDQ(0、4、8、16、24 weeks)
- Percentage of Participants who decrease in VAS scale(0、4、8、16、24 weeks)
- Percentage of Participants who decrease in Wexner incontinence score(0、4weeks)
研究者
Fangyu Wang
Chief of digestive department
Jinling Hospital, China