drugset / Trial / NCT00759200

Safety and Efficacy of Albumin Interferon Administered Every 4 Weeks in Genotype 2/3 Hepatitis C Patients

NCT00759200

Phase 2 Completed 525 enrolled Novartis Human Genome Sciences Inc. · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the safety and efficacy of alb-interferon in adults with genotype 2 or 3 chronic hepatitis

Timeline

Start
2008-10
Primary completion
2010-12
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Albinterferon Alfa-2b Protein / enzyme biologic 900 ug
Subject Albinterferon Alfa-2b Protein / enzyme biologic 1200 ug
Subject Albinterferon Alfa-2b Protein / enzyme biologic 1500 ug
Subject Albinterferon Alfa-2b Protein / enzyme biologic 1800 ug
Comparator Peginterferon alfa-2a Protein / enzyme biologic 180 ug