drugset / Trial / NCT06306339

A Study to Assess the Efficacy and Safety of Burfiralimab (hzVSF-v13) and DMRD (Disease-modifying Antirheumatic Drug)

NCT06306339

Phase 2 Unknown 60 enrolled ImmuneMed, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The goal of this clinical trial is to evaluate the efficacy and safety of intravenous infusions of burfiralimab (hzVSF-v13) when added to Disease-Modifying Antirheumatic Drug (DMARD) treatment as Standard of Care (SOC) in participants with moderate to severe Rheumatoid Arthritis (RA).

Timeline

Start
2024-03
Primary completion
2025-05
Completion
2025-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Burfiralimab Monoclonal antibody 200 mg Intravenous
Subject Burfiralimab Monoclonal antibody 600 mg Intravenous

Indications