drugset / Trial / NCT01452308

Pilot Study of Simtuzumab in the Treatment of Liver Fibrosis

NCT01452308

Phase 2 Completed 20 enrolled Gilead Sciences
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the safety and tolerability of simtuzumab (GS-6624) in patients with fibrosis of the liver. Up to 20 participants will be enrolled into two sequential cohorts. Cohort 1 will consist of 10 participants who will receive simtuzumab every other week for a total of 3 infusions. Participants in Cohort 2 (10 subjects) will also receive simtuzumab every other week for a total of 3 infusions; the dose will depend on the safety and tolerability of simtuzumab seen in Cohort 1. Participants from both cohorts who have completed the main study will be allowed to continue on simtuzumab treatment for an additional extension period, and will receive up to 13 additional infusions of simtuzumab at a fixed dose of 700 mg for an additional 24 weeks.

Timeline

Start
2011-11
Primary completion
2013-01
Completion
2013-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Simtuzumab Monoclonal antibody 10 mg/kg Intravenous
Subject Simtuzumab Monoclonal antibody 700 mg Intravenous