drugset / Trial / NCT06248619

A Trial to Investigate Teprotumumab Subcutaneous Administration Compared With Placebo in Male and Female Adult Participants With Moderate-to-severe Active Thyroid Eye Disease

NCT06248619

Phase 3 Active not recruiting 89 enrolled Amgen
RandomizedParallel-groupTriple-blindTreatment

Summary

The study consists of a randomized double-masked, placebo-controlled, parallel-group, multicenter trial with an optional open-label treatment period for proptosis non-responders who complete the Double-masked Treatment Period.

Timeline

Start
2024-07-05
Primary completion
2025-12-23
Completion
2026-11-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Teprotumumab Monoclonal antibody Subcutaneous