drugset / Trial / NCT05524571

Study to Assess Batoclimab in Participants With Active Thyroid Eye Disease

NCT05524571 ↗

Phase 3 Completed 86 enrolled Immunovant Sciences GmbH
RandomizedParallel-groupTriple-blindTreatment

Summary

To evaluate the efficacy of batoclimab 680 milligrams (mg) subcutaneous (SC) once a week (QW) for 12 weeks followed by 340 mg SC QW for 12 weeks versus placebo on proptosis responder rate at Week 24.

Timeline

Start
2023-01-05
Primary completion
2026-02-03
Completion
2026-03-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Batoclimab Monoclonal antibody 340 mg Subcutaneous