drugset / Trial / NCT03963921

Safety and Tolerability of HepaStem in Patients With Cirrhotic and Pre-cirrhotic NASH Patients

NCT03963921 ↗

Phase 1/2 Completed 23 enrolled Cellaion SA
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Multicenter, open-label, safety and tolerability study of ascending doses of HepaStem in patients with cirrhotic and pre-cirrhotic non-alcoholic steato-hepatitis (NASH) to determine the safety and tolerability of ascending single and repeated doses of HepaStem administered to patients with cirrhotic and pre-cirrhotic non-alcoholic steato-hepatitis (NASH)

Timeline

Start
2019-04-09
Primary completion
2020-05-28
Completion
2020-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject HepaStem Cell therapy — Other