An interventional, single arm, multicenter, phase I/IIa clinical trial to investigate the efficacy and safety of allo-APZ2-ACLF for the treatment of acute-on-chronic liver failure (ACLF)

RHEACELL GmbH & Co. KG0 个研究点目标入组 40 人开始时间: 2020年6月23日最近更新: 2021年4月12日

研究概览

暂无简介。

•1. Male or female patients, aged 20 to 75 years;
•2. Diagnosed ACLF of grade 2 or 3 according to EASL-CLIF definition;
•3. Patients are not eligible for liver transplant (confirmed by transplantation board);
•4. Historical confirmed histology result of liver biopsy or other diagnostic methods (like medical imaging such as computed tomography, ultrasound ect.) to exclude other liver diseases;
•5. Women of childbearing potential must have a negative blood pregnancy test at screening;
•6. Women of childbearing potential and fertile man, and their partners must be willing to use highly effective contraceptive methods during the course of the clinical trial;
•7. Written informed consent from patient, legal or authorized representative or a confirmation of justification of trial participation by an independent medical consultant. In case of confirmation by the independent medical consultant, a deferred informed consent from patient, legal or authorized representative has to be given.
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range 29
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range 11

•1. Patients without cirrhosis;
•2. Patients with ACLF grade 1 according to EASL-CLIF definition;
•3. Patient with septic shock;
•4. Patients with known hepatopulmonal syndrome (HPS);
•5. Patients with known pulmonary embolism that needs anticoagulative treatment;
•6. Patients with pre-existing lung disease with necessity of respiratory support;
•7. Active malignancy or history of malignancy within 5 years prior to trial entry;
•8. Known infection with human immunodeficiency virus (HIV?1, HIV-2);
•9. Any known allergies to components of the IMP;
•10. Current or previous (within 30 days of enrolment) treatment with another IMP, or participation and/or under follow-up in another clinical trial;
•11. Patients anticipated to be unwilling or unable to comply with the requirements of the protocol;
•12. Evidence of any other medical conditions (such as psychiatric illness, physical examination, or laboratory findings) that may interfere with the planned treatment, affect the patient’s compliance, or place the patient at high risk of complications related to the treatment;
•13. Pregnant or nursing women;
•14. Employees of the sponsor, or employees or relatives of the investigator.

发起方