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Completed Phase 4 Interventional Results available

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

ClinicalTrials.gov ID: NCT04583735

Public ClinicalTrials.gov record NCT04583735. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 10:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 4, Randomized, Double-masked, Placebo-controlled, Multicenter Trial to Evaluate the Efficacy and Safety of TEPEZZA® in Treating Patients With Chronic (Inactive) Thyroid Eye Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT04583735
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Amgen
Industry
Enrollment
62 participants

Conditions and interventions

Interventions

Biological · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2, 2021 (Actual)
Primary completion
Mar 17, 2023 (Actual)
Completion
Oct 12, 2023 (Actual)
Last update posted
Jul 1, 2024

2021 – 2023

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
The Private Practice of Raymond Douglas Beverly Hills California 90210 —
Perlman Medical Offices / UCSD La Jolla California 92037 —
MACRO Trials Los Angeles California 90048 —
Univ of Colorado Dept of Ophthalmology Aurora Colorado 80045 —
Bascom Palmer Eye Institute / Univ of Miami Miami Florida 33136 —
Mayo Clinic Rochester Minnesota 55905 —
Washington University St Louis Missouri 63108 —
Las Vegas Endocrinology Las Vegas Nevada 89074 —
Endocrinology Specialists & Thyroid Center Greenville South Carolina 29605 —
Hamilton Eye Institute / U Tennessee Memphis Tennessee 38163 —
Neuro-Eye Clinical Trials Houston Texas 77401 —
Medical College of Wisconsin Milwaukee Wisconsin 52336 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04583735, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 1, 2024 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04583735 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →