Study of VVN001 Ophthalmic Solution in Dry Eye Disease

Phase 2

Completed

Interventions: Drug: Vehicle
Drug: VVN001 Ophthalmic Solution 1%
Drug: VVN001 Ophthalmic Solution 5%

Brief Summary: This is a Phase 2a, multi-center, double-masked, randomized, vehicle-controlled, parallel-group study designed to evaluate the safety and tolerability and to explore the efficacy activity of VVN001 ophthalmic solution versus vehicle in subjects with dry eye disease.

Recruitment & Eligibility

Inclusion Criteria

Provide written informed consent prior to any study-related procedures .
Are 18 years of age or older.
Are willing and able to follow instructions and willing to be present for the required study visits for the duration of the study.
Have a best corrected visual acuity (BCVA), using corrective lenses if necessary, in the qualifying eye(s) of +0.7 or better as assessed by Early Treatment of Diabetic Retinopathy Study (ETDRS) at the screening visit and randomization visit.
Have a history of dry eye disease in both eyes
Are currently using artificial tears and have been using within 30 days of the screening visit.
Have an Eye dryness score ≥40 at Visit 1 and ≥35 at Visit 2, one score for both eyes (0-100 point VAS)
Have ongoing dry eye disease in the same eye or both eyes, as defined by all of the following criteria in the study eye and the same eye at Visit 1 and Visit 2:
Inferior CFS (iCFS) score of ≥2 (NEI; 0-4 scale; using 0.5 unit increments)
Have a Schirmer score (without anesthesia) of ≥1 and ≤7 mm/5 min.

Exclusion Criteria

Have a known hypersensitivity or contraindication to the IP or components of IP.
Have a Schirmer score (without anesthesia) of <1 or >7 mm/5 min in the study eye.
Have history of uncontrolled glaucoma, IOP over 21 mmHg in either eye at the screening visit or are being treated with eye drops for glaucoma in the study eye. Or the subject has had laser or surgery for glaucoma in the study eye within 90 days of the study.

Arm && Interventions

Group	Intervention	Description
Vehicle	Vehicle	VVN001 Ophthalmic Solution Placebo
VVN001, 1%	VVN001 Ophthalmic Solution 1%	VVN001, 1% ophthalmic solution
VVN001, 5%	VVN001 Ophthalmic Solution 5%	VVN001, 5% ophthalmic solution

Primary Outcome Measures

Name	Time	Method
Inferior Corneal Fluorescein Staining	Day 84	Mean change from baseline in Inferior corneal fluorescein staining. Negative number indicates improvement. Depending upon individual subject's baseline, this measure can range from -4 to +4.

Secondary Outcome Measures

Name	Time	Method
Total Corneal Fluorescein Staining	Day 84	Mean change from baseline in total corneal fluorescein staining Negative number indicates improvement. Depending upon individual subject's baseline, this measure can range from -20 to +20.
Regional Corneal Fluorescein Staining	Day 84	Mean change from baseline in temporal regional corneal fluorescein staining. Negative number indicates improvement. Depending upon individual subject's baseline, this measure can range from -4 to +4.
Eye Dryness	Day 84	Mean Change in Eye Dryness VAS. Negative number indicates improvement. Depending upon individual subject's baseline, this measure can range from -100 to +100..