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Clinical trialNCT03764735CompletedPhase 3Interventional

Study of SkQ1 as Treatment for Dry-eye Syndrome

SponsorMitotech, SAEnrollment452Dry Eye Syndrome
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to evaluate whether SkQ1 ophthalmic solutions are safe and effective compared to placebo for the treatment of the signs and symptoms of dry eye syndrome.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

7 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Cornea & Cataract Consultants of Arizona

    Phoenix, Arizona, United States

  • Eye Research Foundation

    Newport Beach, California, United States

  • Eye Care Insititute

    Louisville, Kentucky, United States

  • Central Maine Eye Care

    Lewiston, Maine, United States

  • Andover Eye Associates

    Andover, Massachusetts, United States

  • Vita Eye Clinic

    Shelby, North Carolina, United States

  • Total Eye Care, Pa

    Memphis, Tennessee, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

High dose - SkQ1Low Dose - SkQ1SkQ1
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
6 Dec 2018
Primary completion
9 Feb 2019
Completion
9 Feb 2019
Last update posted
19 Jan 2022
Registered enrollment
452
Registry id
NCT03764735

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.