drugset / Trial / NCT00473824

Randomized Phase II Study of Hepatitis C Immune Globulin Intravenous (Human), Civacir(TM), in Liver Transplantation

NCT00473824 ↗

Phase 2 Terminated 7 enrolled ADMA Biologics, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

A Phase 2 study to evaluate safety, pharmacokinetics and efficacy of Hepatitis C Immune Globulin Intravenous (human) \[Civacir(TM)\] for preventing or reducing the impact of recurrent HCV infection following liver transplantation.

Timeline

Start
2007-05
Primary completion
2009-02
Completion
2009-02

Outcome

Outcome not reported

Stopped: “New sponsor's decision to pursue a redesigned clinical study”

Drugs

EvaluationDrugModalityDoseRoute
Subject Civacir® Unknown 300 mg/kg Intravenous
Subject Civacir® Unknown 400 mg/kg Intravenous