NCT05836883终止1 期
A Phase IB/IIA Study of ExoFlo, an Ex Vivo Culture-expanded Adult Allogeneic Bone Marrow Mesenchymal Stem Cell Derived Extracellular Vesicle Isolate Product, for the Treatment of Perianal Fistulizing Crohn's Disease
适应症
干预措施
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 入组人数
- 5
- 试验地点
- 1
- 主要终点
- Adverse Events
研究概览
简要总结
To evaluate the safety and feasibility of ExoFlo as a treatment for Perianal Fistulizing Crohn's Disease.
详细描述
This is a phase IB/IIA, multicenter, single-blind, placebo-controlled, dose-escalation design, randomized controlled trial for the treatment of Perianal Fistulizing Crohn's Disease.
Subjects will be randomized 2:1 Investigational Medicinal Product (IMP) to normal saline (NS) in cohorts of 12 subjects as follows:
Cohort 1: Local injection of 15 mL of IMP or NS on Day 0 (8 IMP, 4 NS)
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- Single (Participant)
盲法说明
Single-blind
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Men and Women 18-75 years of age with a diagnosis of Crohn's Disease (CD) for at least six months duration.
- •Single and/or Multi-tract Perianal fistula(s).
- •Failed at least one medical therapy within the last year including, but not limited to, antibiotics, immunomodulators (6-MP, methotrexate, azathioprine), monoclonal antibodies (infliximab, adalimumab, certolizumab, ustekinumab, golimumab, vedolizumab), or small molecule inhibitors.
- •Previous failed surgical intervention, including seton placement at least two weeks prior, or are not candidates for surgical intervention or are not willing to undergo surgical intervention for the management of their fistula.
- •Medical therapy for CD stable for at least 2 months prior to administration of IMP. Changes in dosing or dosing intervals related to serum drug levels are permitted.
- •Ability to comply with protocol.
- •Competent and able to provide written informed consent.
排除标准
- •Active perianal abscess or infection at the time of screening, enrollment, or at the time of investigational product administration
- •Clinically significant medical conditions within the six months before administration of IMP that would, in the opinion of the investigators, compromise the safety of the subject.
- •History of cancer including melanoma (with the exception of localized skin cancers) within one year of screening.
- •History of colorectal cancer within 2 years
- •Subjects who have a diagnosis of coagulation disorders and/or are currently on anti-coagulant therapy
- •Investigational drug within one month of treatment
- •Pregnant or breast feeding or trying to become pregnant.
- •Presence of a rectovaginal fistula
- •Presence of an ileal anal pouch and/or history of proctectomy
- •The presence of severe proctitis
- •Any condition which, in the opinion of the investigator, would make it unsafe or unsuitable for patients to undergo Magnetic Resonance (MR) evaluations (i.e., presence of implantable or external MR unsafe device that cannot be removed, body weight exceeding limitations, claustrophobia etc.).
- •A participant who is unwilling to use medically acceptable contraception methods during participation in study
- •The following out of range laboratory results at screening (result may be repeated)
- •WBC >11 x 109 /L
- •Hemoglobin < 8 g/dl
- •Platelet count <100,000/mL
- •AST/ALT >2 times the upper limit of normal
- •Creatinine >2 umol/L
- •PT/INR: outside normal limits
- •Hemoglobin A1c>6.5 mg/dL
研究组 & 干预措施
Cohort 1: Placebo
Placebo Comparator
Local injection 15 mL of normal saline on Day 0
干预措施: Local injection of normal saline (Other)
Cohort 1: Treatment
Experimental
Local injection of 15 mL of ExoFlo on Day 0
干预措施: ExoFlo (Biological)
结局指标
主要结局
Adverse Events
时间窗: 3 Months
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
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