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Completed Phase 3 Interventional Results available

CyclASol for the Treatment of Signs and Symptoms of Dry Eye Disease in Subjects Who Completed CYS-004

ClinicalTrials.gov ID: NCT04523142

Public ClinicalTrials.gov record NCT04523142. 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 May 16, 2026, 5:54 AM 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, Open-label, Single-arm Clinical Trial to Assess the Long-term Safety and Tolerability of Topical CyclASol® for the Treatment of Dry Eye Disease in Subjects Who Completed the Clinical Trial CYS-004

Study identification

NCT ID
NCT04523142
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novaliq GmbH
Industry
Enrollment
202 participants

Conditions and interventions

Interventions

  • CyclASol Ophthalmic Solution Drug

Drug

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
Jan 3, 2021
Primary completion
Apr 29, 2022
Completion
May 22, 2022
Last update posted
Oct 15, 2023

2021 – 2022

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
CYS-005 Investigational Site Los Angeles California 90013
CYS-005 Investigational Site Newport Beach California 92663
CYS-005 Investigational Site Carmel Indiana 46290
CYS-005 Investigational Site Louisville Kentucky 40206
CYS-005 Investigational Site Andover Massachusetts 01810
CYS-005 Investigtional Site Raynham Massachusetts 02767
CYS-005 Investigational Site Henderson Nevada 89052
CYS-005 Investigational Site Raleigh North Carolina 27603
CYS-005 Investigational Site Shelby North Carolina 28150
CYS-005 Investigational Site Fargo North Dakota 58103
CYS-005 Investigational Site Cranberry Township Pennsylvania 16066
CYS-005 Investigational Site Memphis Tennessee 38119
CYS-005 Investigational Site Layton Utah 84041
CYS-005 Investigational Site Lynchburg Virginia 24502

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 NCT04523142, 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 Oct 15, 2023 · Synced May 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04523142 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →