A Phase 1 Study to evaluate the Safety of teprotumumab in Patients with Diabetic Macular Edema.
A Phase 1, Open-Label Safety and Pharmacodynamic Study of RV 001, an Insulin-Like Growth Factor-1 Receptor (IGF-1) Antagonist, Given By IV Infusion in Patients with Diabetic Macular Edema (DME).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
Teprotumumab 20mg/kg administered by intravenous infusion every 3 weeks for 3 infusions
David S Boyer
Beverly Hills, California, United States
David A Eichenbaum, MD
St. Petersburg, Florida, United States
Diana Do, MD
Omaha, Nebraska, United States
Safety of RV001in subjects with Diabetic Macular Edema
Number of subjects with adverse events, serious adverse events and early discontinuations due to adverse events. Number of subjects with clinical significant abnormal laboratory values, electrocardiograms (pre and post infusions), abnormal vital signs, ophthalmic and physical examinations.
Time frame: Change from Baseline to Week 9
Safety of RV001in subjects with Diabetic Macular Edema
Pharmacodynamic measure includes change in Optical Coherence Tomography, Fluorescein Angiography and Stereoscopic color funds photos findings.
Time frame: Change from Baseline to Week 9
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