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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05517421
Study type Interventional
Source Immunovant Sciences GmbH
Contact Central Study Contact
Phone 18007970414
Email clinicaltrials@immunovant.com
Status Recruiting
Phase Phase 3
Start date November 23, 2022
Completion date January 2025

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