跳至主要内容
临床试验/CTRI/2020/01/022743
CTRI/2020/01/022743招募中1 期

An open label, single arm, investigator initiated Phase I/II study to assess the safety and efficacy of local administration of stempeucel® (Adult Human Bone Marrow Derived, Cultured, Pooled, Allogeneic Mesenchymal Stromal Cells) in Patients with Perianal Fistulizing Crohnâ??s disease

All India Institute of Medical Sciences0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
招募中

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. A signed and dated informed consent form and audio visual consent has been obtained from the patient. 2. Patient is able and willing to comply with study procedures 3. Males or females (willing to use accepted methods of contraception during the course of the study) in the age group of 18-65 years. 4. Diagnosed with a complex perianal fistula associated with Crohnâ??s Disease of at least 3 months before screening visit with a maximum of 1 internal openings and a maximum of 2 external openings. 5. Actively draining fistulas. 6. Patients whose perianal fistula were previously treated and are refractory to medical therapy (antibiotics for 1 month or immunomodulators for 3 months or on biological therapy (TNF â?? ? antagonist) or surgical therapy and has shown or have documented intolerance. Note: Definition of complex fistula: Complex fistulae are high (high inter-sphincteric, high intra-sphincteric, suprasphincteric or extra-sphincteric) and/or can have several external openings, may be associated with a perianal abscess, connection to the vagina or bladder, rectal stenosis or macroscopic proctitis.

排除标准

  • 1. Crohnâ??s Disease Activity Index (CDAI) score ? 220. 2. Perianal abscess > 2 cm in diameter. 3. Presence of proctitis, anal canal stricture and fistulas other than perianal fistulas. 4. Received steroids within 1 month prior to enrolment or who has not received any treatment for perianal fistulas. 5. Presence of other autoimmune diseases, active tuberculosis. 6. Patients allergic to bovine serum. 7. Patient with known hypersensitivity to the constituents of the IMP â?? DMSO, Dextran 40, CryoStor® - CS5. 8. Pregnant and lactating women. 9. Patients already enrolled in another investigational drug trial or completed within 3 months or those who have participated in any stem cell clinical trial any time in the past. 10. Patient has a current or past history of any cancer. 11. Patients with Hb 12. Patientâ??s serum bilirubin level 2 times more than upper normal limit. 13. Patient has any of the following unstable conditions or circumstances that could interfere with the standard care of treatment: • Inability to comply with treatment visit schedule • Mental incapacity • Current substance abuse 14. Positive for HIV, HCV, HBV, VDR

研究者

相似试验