drugset / Trial / NCT03298867

Treatment of Graves' Orbitopathy (Thyroid Eye Disease) to Reduce Proptosis With Teprotumumab Infusions in a Randomized, Placebo-Controlled, Clinical Study

NCT03298867

Phase 3 Completed 83 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The overall objective is to investigate the efficacy, tolerability, and safety of teprotumumab (a fully human monoclonal antibody \[mAb\] inhibitor of the insulin-like growth factor-1 receptor \[IGF-1R\]) administered once every 3 weeks (q3W) for 21 weeks with a final assessment at Week 24, in comparison to placebo, in the treatment of participants with moderate-to-severe active thyroid eye disease (TED).

Timeline

Start
2017-10-04
Primary completion
2019-02-13
Completion
2020-11-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Teprotumumab Monoclonal antibody 20 mg/kg Intravenous