drugset / Trial / NCT06401044

A Study of AMG 732 in Healthy Participants and Participants With Thyroid Eye Disease

NCT06401044 ↗

Phase 1/2 Recruiting 88 enrolled Amgen
RandomizedSequentialDouble-blindTreatment

Summary

The primary objective of Part A of this study is to investigate the safety and tolerability of AMG 732 after single subcutaneous (SC) doses. The primary objective of Part B of this study is to investigate the efficacy of AMG 732 in participants with Thyroid Eye Disease (TED) after multiple SC doses.

Timeline

Start
2024-05-30
Primary completion
2027-02-22
Completion
2027-08-13

Drugs

EvaluationDrugModalityDoseRoute
Subject AMG 732 Unknown — Subcutaneous