Vehicle-Controlled Study of SkQ1 as Treatment for Dry-eye Syndrome

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

610 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-12-20

Study Completion Date

2020-10-06

Brief Summary

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The purpose of this study is to evaluate whether SkQ1 Ophthalmic Solution is safe and effective compared to Vehicle for the treatment of the signs and symptoms of dry eye syndrome.

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Detailed Description

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Multi-center, double-masked, randomized, placebo-controlled study comprising 5 visits over the course of approximately 9 weeks. Qualified subjects are randomized 1:1 to receive either SkQ1 Ophthalmic Solution, or Placebo (vehicle of SkQ1 Ophthalmic Solution).

The Primary Endpoints are:

Change from Baseline (Visit 2) to Visit 5 of Ocular Discomfort;

Change from Baseline (Visit 2) to Visit 5 of conjunctival fluorescein staining (sum of temporal and nasal regions)

Conditions

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Dry Eye Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Parallel Assignment Parallel-group study SkQ1 Ophthalmic Solution versus placebo (vehicle) solution

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Placebo Comparator: SkQ1 Vehicle

Vehicle for SkQ1 Ophthalmic Solution

Group Type PLACEBO_COMPARATOR

SkQ1 Vehicle Solution

Intervention Type DRUG

SkQ1 Ophthalmic Solution Vehicle

SkQ1

SkQ1 Ophthalmic Solution

Group Type ACTIVE_COMPARATOR

SkQ1 Ophthalmic Solution

Intervention Type DRUG

SkQ1 Ophthalmic Solution

Interventions

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SkQ1 Vehicle Solution

SkQ1 Ophthalmic Solution Vehicle

Intervention Type DRUG

SkQ1 Ophthalmic Solution

Intervention Type DRUG

Other Intervention Names

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Vehicle for SkQ1 Visomitin

Eligibility Criteria

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Inclusion Criteria

* Be at least 18 years of age;
* Provide written informed consent;
* Have a subject reported history of dry eye;
* Have a history of use of eye drops for dry eye symptoms;
* Ocular Discomfort;
* Schirmer's Test score;
* Have corneal fluorescein staining ;
* Have lissamine green conjunctival Staining;
* Have a conjunctival redness;

Exclusion Criteria

* Have been previously exposed to previous SkQ1 Ophthalmic Solution treatment;
* Have any clinically significant slit lamp findings at Visit 1;
* Be diagnosed with an ongoing ocular infection or active ocular inflammation at Visit 1;
* Have had any ocular and/or lid surgeries within 6 months of Visit 1 or any planned over the study period;
* Have an uncontrolled systemic disease;
* Be a woman who is pregnant, nursing or planning a pregnancy;
* Be a woman of childbearing potential who is not using an acceptable means of birth control;
* Have a known allergy and/or sensitivity to the study drug or its components;
* Have a condition or be in a situation which the investigator feels may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study;
* Be currently enrolled in an investigational drug or device study or have used an investigational drug or device within 30 days of Visit 1;

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No