HomeTrialNCT06401044
🔬NCT06401044Phase 1Phase 2RECRUITING

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

Study 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.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment88 participants
Primary Completion
Lead SponsorAmgen
Data Retrieved2026-04-13 18:29:34.157629+00:00
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