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Teprotumumab Treatment in Patients With Active Thyroid Eye Disease

Study:

A Multicenter, Double-masked, Placebo-controlled, Efficacy and Safety Study of an Insulin-like Growth Factor-1 Receptor (IGF-1R) Antagonist Antibody (Fully Human), in Patients With Active Thyroid Eye Disease

Rationale:

n/a

Purpose:

The purpose of this study is to evaluate the safety, tolerability and effectiveness of a fully human antibody compared to placebo in the treatment of patients with active thyroid eye disease.

Study Status: Recruiting

Recruiting:
n/a

Condition Intervention Phase
Thyroid Associated Ophthalmopathies
Thyroid-Associated Ophthalmopathy
Drug: teprotumumab
Drug: Placebo
Phase 2

Verified by River Vision Development Corporation June, 2013

Sponsored by: River Vision Development Corporation
Information provided by: River Vision Development Corporation
ClinicalTrials.gov identifier: NCT01868997

Study Type: Interventional

Study Design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Cole Eye Institute at Cleveland Clinic
Cleveland, Ohio 44195
United States

Raymond S Douglas, MD,PhD., Principal Investigator

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.

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