National Collaborative Centre for Hepatic Regenerative Medicine (NC-CHRM): Phase I Study on Safety and Efficacy of Mesenchymal Stem-Cell (MSC) Therapy in Non-Viral Acute-on-Chronic Liver Failure (ACLF)

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

January 31, 2026

Primary Completion Date

December 31, 2031

Study Completion Date

December 31, 2031

Conditions
Acute-On-Chronic Liver Failure
Interventions
DRUG

umbilical cord Mesenchymal Stem Cell

To test the safety and tolerability of ucMSC 1 million/kg will be given intra-venously once a week for 4 week in 10 ACLF patients. 250 ml normal saline will be infused 30 minutes prior to ucMSCs infusion. The fresh ucMSCs will be taken from ILBS cGMP facility and will be infused through IV canula peripherally over 30 minutes followed by a further 250 ml normal saline over 20-30 minutes.

All Listed Sponsors
collaborator

Indian Council of Medical Research

OTHER_GOV

lead

Institute of Liver and Biliary Sciences, India

OTHER