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Completed Phase 3 Interventional Results available

Tavilermide Ophthalmic Solution for the Treatment of Dry Eye

ClinicalTrials.gov ID: NCT03925727

Public ClinicalTrials.gov record NCT03925727. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 2:21 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multi-Center, Randomized,Double-Masked, Vehicle-Controlled Study to Assess the Safety and Efficacy Study of Tavilermide Ophthalmic Solutions for the Treatment of Dry Eye

Study identification

NCT ID
NCT03925727
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Mimetogen Pharmaceuticals USA, Inc.
Industry
Enrollment
623 participants

Conditions and interventions

Interventions

  • Tavilermide ophthalmic solution Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 99 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 27, 2019
Primary completion
Jun 10, 2020
Completion
Jun 10, 2020
Last update posted
Apr 4, 2023

2019 – 2020

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Tavilermide Investigational Site Phoenix Arizona 85032
Tavilermide Investigational Site Los Angeles California 90013
Tavilermide Investigational Site Newport Beach California 92663
Tavilermide Investigational Site Fort Collins Colorado 80528
Tavilermide Investigational Site Littleton Colorado 80120
Tavilermide Investigational Site Boynton Beach Florida 33437
Tavilermide Investigational Site Bradenton Florida 34209
Tavilermide Investigational Site Coral Springs Florida 33067
Tavilermide Investigational Site Ocala Florida 34474
Tavilermide Investigational Site Indianapolis Indiana 46290
Tavilermide Investigational Site Sioux City Iowa 51104
Tavilermide Investigational Site Lexington Kentucky 40509
Tavilermide Investigational Site Louisville Kentucky 40206
Tavilermide Investigational Site St Louis Missouri 63131
Tavilermide Investigational Site Shelby North Carolina 28150
Tavilermide Investigational Site Cincinnati Ohio 45236
Tavilermide Investigational Site Mason Ohio 45040
Tavilermide Investigational Site Rapid City South Dakota 57701
Tavilermide Investigational Site Maryville Tennessee 37803
Tavilermide Investigational Site Nashville Tennessee 37205
Tavilermide Investigational Site San Antonio Texas 78248
Tavilermide Investigational Site Kenosha Wisconsin 53142

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03925727, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 4, 2023 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03925727 live on ClinicalTrials.gov.

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