Real World Study to Describe the Effectiveness and Safety of Teprotumumab Among Thyroid Eye Disease Patients

NCT07085117 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5

Last updated 2025-09-08

No results posted yet for this study

Summary

The main objective of this study is to assess the number of participants with proptosis response as of last intravenous infusion of teprotumumab.

Conditions

  • Thyroid Eye Disease

Interventions

DRUG

Teprotumumab

Participants received teprotumumab as an intravenous (IV) infusion.

Sponsors & Collaborators

Principal Investigators

  • MD · Amgen

Eligibility

Min Age
18 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-02
Primary Completion
2025-08-10
Completion
2025-08-10
FDA Drug
Yes

Countries

  • China

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07085117 on ClinicalTrials.gov