drugset / Trial / NCT05907668

A Proof-of-Concept Study to Assess Batoclimab in Participants With Graves' Disease

NCT05907668 ↗

Phase 2 Completed 35 enrolled Immunovant Sciences GmbH
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the efficacy and safety of 24 weeks of treatment with batoclimab in adult participants with biochemically documented hyperthyroidism due to GD who have failed to achieve euthyroidism on antithyroid drugs (ATDs).

Timeline

Start
2023-05-15
Primary completion
2025-07-25
Completion
2025-07-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Batoclimab Monoclonal antibody 340 mg Subcutaneous

Indications