drugset / Trial / NCT06389578

A Study of TEPEZZA® Treatment in Participants With Thyroid Eye Disease

NCT06389578

Phase 1 Completed 16 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

The main goal of this study is to learn how teprotumumab will be processed in the body (Pharmacokinetics) subcutaneously and whether it is safe and tolerable after administration into adult patients with thyroid eye disease.

Timeline

Start
2022-07-14
Primary completion
2023-02-28
Completion
2023-09-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Teprotumumab Monoclonal antibody Subcutaneous