drugset / Trial / NCT05686759

A Study to Investigate the Safety and Efficacy of Undiluted Intravenous Infusion of I.V.-Hepabig Inj.

NCT05686759 ↗

Phase 3 Recruiting 105 enrolled GC Biopharma Corp
RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the efficacy and safety of undiluted intravenous infusion of I.V.-Hepabig inj. in post-liver transplant patients

Timeline

Start
2023-04-13
Primary completion
2026-06-30
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Hepabig Unknown 10000 iu Intravenous