drugset / Trial / NCT04521114

Leronlimab (PRO 140) in Patients With Nonalcoholic Steatohepatitis

NCT04521114 ↗

Phase 2 Completed 87 enrolled CytoDyn, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a phase II study of of Leronlimab (PRO 140)-Humanized monoclonal antibody to CCR5 in patients with Nonalcoholic Steatohepatitis (NASH).

Timeline

Start
2020-12-01
Primary completion
2021-12-29
Completion
2021-12-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Leronlimab Monoclonal antibody 350 mg Subcutaneous
Subject Leronlimab Monoclonal antibody 700 mg Subcutaneous