학술논문

Topical Recombinant Human Nerve Growth Factor (Cenegermin) for Neurotrophic Keratopathy A Multicenter Randomized Vehicle-Controlled Pivotal Trial
Document Type
article
Source
Ophthalmology. 127(1)
Subject
Biomedical and Clinical Sciences
Ophthalmology and Optometry
Clinical Trials and Supportive Activities
Physical Injury - Accidents and Adverse Effects
Eye Disease and Disorders of Vision
Neurosciences
Clinical Research
Evaluation of treatments and therapeutic interventions
6.1 Pharmaceuticals
Eye
Administration
Ophthalmic
Adult
Aged
Aged
80 and over
Cornea
Corneal Ulcer
Double-Blind Method
Epithelium
Corneal
Female
Fluorophotometry
Follow-Up Studies
Humans
Male
Middle Aged
Nerve Growth Factor
Ophthalmic Solutions
Recombinant Proteins
Treatment Outcome
Trigeminal Nerve Diseases
Visual Acuity
Wound Healing
Clinical Sciences
Opthalmology and Optometry
Public Health and Health Services
Ophthalmology & Optometry
Ophthalmology and optometry
Language
Abstract
PURPOSE:To evaluate the efficacy and safety of topical cenegermin (recombinant human nerve growth factor) in patients with neurotrophic keratopathy. DESIGN:Multicenter, randomized, double-masked, vehicle-controlled trial. PARTICIPANTS:Patients with neurotrophic persistent epithelial defect with or without stromal thinning. METHODS:The NGF0214 trial, conducted among 11 sites in the United States, randomized 48 patients 1:1 to cenegermin 20 μg/ml or vehicle eye drops, 6 drops daily for 8 weeks of masked treatment. Follow-up was 24 weeks. Safety was assessed in all patients who received study drug. Efficacy was assessed by intention to treat. MAIN OUTCOME MEASURES:The primary end point was healing of the neurotrophic lesion (persistent epithelial defect or corneal ulcer) after 8 weeks of masked treatment. Masked central readers measured neurotrophic lesions in randomized clinical pictures, then assessed healing status conventionally (