drugset / Trial / NCT05015127

A Study to Evaluate the Efficacy and Safety of HBM9161 on Moderate to Severe Thyroid Eye Disease

NCT05015127 ↗

Phase 2/3 Unknown 36 enrolled Harbour BioMed (Guangzhou) Co. Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objective: To preliminarily evaluate the efficacy of the treatment regimen of HBM9161 680 mg administered subcutaneously weekly and sequentially every other week for 12 weeks in Chinese patients with active moderate to severe TED.

Timeline

Start
2021-09-22
Primary completion
2022-10
Completion
2022-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Batoclimab Monoclonal antibody 680 mg Subcutaneous