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A Clinical Trial Assessing the Safety, Tolerability, and Exploratory Efficacy of a Novel Bioartificial Liver Therapy in Patients With Liver Failure or Small-for-Size Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The goal of this clinical trial is to evaluate the safety and tolerability of a novel bioartificial liver (CiPS-BAL) in patients with liver failure or small-for-size syndrome. The study will also collect preliminary data on clinical outcomes and laboratory parameters during treatment. The main questions it aims to answer are: Is the novel bioartificial liver system safe and well tolerated in patients with liver failure or small-for-size syndrome? What effects does the treatment have on liver function and other clinical and laboratory indicators? Researchers will treat participants with the CiPS-BAL system, which uses hepatocytes derived from chemically induced pluripotent stem cells (CiPS) within a bioartificial liver device.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Patients diagnosed with liver failure (including acute, subacute/acute-on-chronic, and chronic liver failure) or small-for-size syndrome

Locations
Other Locations
China
Beijing Friendship Hospital
RECRUITING
Beijing
Contact Information
Primary
Wan-Ting Zhang
13699189579@163.com
+86 13699189579
Time Frame
Start Date: 2025-12-01
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 12
Treatments
Experimental: CiPS-BAL
Chemically induced pluripotent stem cells biological Artificial Liver
Related Therapeutic Areas
Sponsors
Leads: Beijing Friendship Hospital

This content was sourced from clinicaltrials.gov

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