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Completed Phase 3 Interventional Results available

ESSENCE 2: CyclASol for the Treatment of Signs and Symptoms of Dry Eye Disease (DED)

ClinicalTrials.gov ID: NCT04523129

Public ClinicalTrials.gov record NCT04523129. 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 Sep 3, 2026, 3:53 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

A Phase 3, Multi-center, Randomized, Double-masked, Vehicle-controlled Clinical Trial to Assess the Efficacy and Safety of Topical CyclASol® for the Treatment of Dry Eye Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this pivotal trial is to assess the efficacy, safety and tolerability of CyclASol in comparison to the vehicle for the treatment of signs and symptoms of Dry Eye Disease (DED).

Study identification

NCT ID
NCT04523129
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novaliq GmbH
Industry
Enrollment
834 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Dec 4, 2020
Primary completion
Sep 2, 2021
Completion
Oct 7, 2021
Last update posted
Mar 9, 2023

2020 – 2021

United States locations

U.S. sites
27
U.S. states
19
U.S. cities
26
Facility City State ZIP Site status
CYS-004 Investigational Site Phoenix Arizona 85032
CYS-004 Investigational Site Los Angeles California 90013
CYS-004 Investigational Site Newport Beach California 92663
CYS-004 Investigational Site Santa Ana California 92705
CYS-004 Investigational Site Colorado Springs Colorado 80907
CYS-004 Investigational Site Fort Lauderdale Florida 33309
CYS-004 Investigational Site Chicago Illinois 60619
CYS-004 Investigational Site Carmel Indiana 46290
CYS-004 Investigational Site Indianapolis Indiana 46240
CYS-004 Investigational site Louisville Kentucky 40206
CYS-004 Investigational Site Andover Massachusetts 01810
CYS-004 Investigational Site Raynham Massachusetts 02767
CYS-004 Investigational Site Medina Minnesota 55364
CYS-004 Investigational Site Kansas City Missouri 64111
CYS-004 Investigation Site Kansas City Missouri 64154
CYS-004 Investigational Site Henderson Nevada 89052
CYS-004 Investigational Site Raleigh North Carolina 27603
CYS-004 Investigational Site Shelby North Carolina 28150
CYS-004 Investigational Site Fargo North Dakota 58103
CYS-004 Investigational Site Cranberry Township Pennsylvania 16066
CYS-004 Investigational Site Warwick Rhode Island 02886
CYS-004 Investigational Site Memphis Tennessee 38119
CYS-004 Investigational Site Smyrna Tennessee 37167
CYS-004 Investigational Site Layton Utah 84041
CYS-004 Investigational site Ogden Utah 84403
CYS-004 Investigational Site Lynchburg Virginia 24502
CYS-004 Investigational Site Seattle Washington 98119

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 NCT04523129, 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 Mar 9, 2023 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04523129 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →