The objective of this study is to obtain initial efficacy of BRM424 in patients with Stage 2 and Stage 3 NK and evaluate safety and tolerability.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
12
A topical drop of BRM424 ophthalmic solution.
A topical drop of BRM424 ophthalmic solution.
Wilmington Eye
Leland, North Carolina, United States
RECRUITINGProportion of patients achieving complete healing of the PED or corneal ulcer determined by corneal fluorescein staining
Time frame: at or before 4 weeks
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