Real World Study to Describe the Effectiveness and Safety of Teprotumumab Among Thyroid Eye Disease Patients
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Phase
—
Status
Completed
Study type
Observational
Enrollment
5actual
Sites
1
Country
China
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2025-07-02 | actual | When the study began enrolling |
| Primary completion | 2025-08-10 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-08-10 | actual | The whole study's end, after follow-up |
| First posted | 2025-07-25 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-09-08 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Thyroid Eye Disease
Intervention
- Drug: Teprotumumab — also filed as TEPEZZA®
Primary outcome
what the primary-completion date above is the date OFNumber of Participants with Proptosis Response as of the Last IV Infusion Teprotumumab
measured From baseline up to approximately 3 years
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