The main goal of this study is to learn how teprotumumab will be processed in the body (Pharmacokinetics) subcutaneously and whether it is safe and tolerable after administration into adult patients with thyroid eye disease.
This is a Phase 1b, open-label, multicenter trial to assess the PK, safety, and tolerability of a single SC dose of lyophilized teprotumumab and high concentration formulation teprotumumab in participants with thyroid eye disease. Approximately 6 participants (in Cohort 1) and approximately 10 participants (in Cohort 2) who meet the trial eligibility criteria will be enrolled in a 1:1 ratio. Study acquired from Horizon in 2024.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
SC administration and IV infusion
Bascom Palmer Eye Institute - University of Miami
Miami, Florida, United States
Barnes Jewish Hospital Washington University
St Louis, Missouri, United States
Neuro-Eye Clinical Trials
Bellaire, Texas, United States
Pharmacokinetics (PK): Area Under the Curve (AUC) of Teprotumumab
AUC will be evaluated from the collected PK samples.
Time frame: Pre dose through Week 6
PK: Maximum Serum Concentration (Cmax) of Teprotumumab
Cmax will be evaluated from the collected PK samples.
Time frame: Pre dose through Week 6
Number of Participants With Adverse Events (AE)
An AE is any untoward medical occurrence in a participant or clinical investigation subject administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE can, therefore, be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom or disease temporally associated with the use of a medicinal (investigational) product, whether or not considered related to the medicinal (investigational) product.
Time frame: Up to Week 6
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