drugset / Trial / NCT04583735

A Study Evaluating TEPEZZA® Treatment in Patients With Chronic (Inactive) Thyroid Eye Disease

NCT04583735

Phase 4 Completed 62 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The overall objective is to investigate the efficacy, safety and tolerability of TEPEZZA® in participants with chronic (inactive) TED (thyroid eye disease). Approximately 57 participants will be enrolled. There will be a treatment period (through Week 24) and a follow up period (where TEPEZZA will not be infused).

Timeline

Start
2021-09-02
Primary completion
2023-03-17
Completion
2023-10-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Teprotumumab Monoclonal antibody 20 mg/kg Intravenous