The purpose of this study is to assess the safety and tolerability of ocular administration of Topical Interleukin-1-Receptor Antagonist in healthy volunteers. Additionally, the PK of Interleukin-1-Receptor Antagonist will be assessed.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Masking
NONE
Enrollment
34
custom eye drop to be applied to the left eye.
Beijing TongRen Hospital
Beijing, China
RECRUITINGCorneal fluorescein staining
Time frame: 3 days
Best corrected visual acuity
Time frame: 3 days
Ocular symptomatology
Time frame: 3 days
Slit lamp examination
Time frame: 3 days
Measurement of intraocularpressure
Time frame: 3 days
ELISA based assay to determine Pharmacokinetics for the evaluation of systemic exposure of IL-1Ra in healthy volunteers.
Time frame: 3 days
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