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Recruiting Phase 3 Interventional

An Efficacy and Safety Study of Cenegermin Ophthalmic Solution Compared With Vehicle in the Treatment of PCED

ClinicalTrials.gov ID: NCT07519902

Public ClinicalTrials.gov record NCT07519902. 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 5, 2026, 11:16 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

Phase 3, Multicenter, Randomized, Double-Masked, Vehicle-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of Recombinant Human Nerve Growth Factor Eye Drop Solution in Participants With Persistent Corneal Epithelial Defect (PCED)

Brief summary

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

This is a phase 3, randomized, multicenter, double-masked, parallel group, vehicle-controlled prospective clinical trial to evaluate the safety and efficacy of cenegermin in inducing complete epithelial healing in participants with PCED. The primary objective is the evaluation of complete epithelial healing after 4 weeks of treatment. The study is comprised of 3 periods: an 8-week initial treatment period (Day 1 to Week 8), an 8-week extension treatment period (Week 9 to Week 16), and a 24-week follow-up period (Week 17 to Week 40).

Study identification

NCT ID
NCT07519902
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Dompé Farmaceutici S.p.A
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

Drug · Other

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
Jun 1, 2026
Primary completion
Nov 30, 2027
Completion
Nov 30, 2027
Last update posted
Jul 15, 2026

2026 – 2027

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Azul Vision, INC Huntington Beach California 92647 Recruiting
Harvard Eye Associates Laguna Hills California 92653 Recruiting
Loma Linda University Adventist Health Sciences Center Loma Linda California 92354 Not yet recruiting
UCLA - Jules Stein Eye Institute (JSEI) - Diabetic Eye Dise Los Angeles California 90095 Not yet recruiting
California Eye Specialists Medical Group, Inc. Redlands California 92373 Recruiting
East Coast Institute for Research - Florida Eye Specialists Jacksonville Florida 32207 Recruiting
Bascom Palmer Eye Institute, University of Miami School of Medicine Miami Florida 33136 Recruiting
University of South Florida Tampa Florida 33620 Recruiting
Massachusetts Eye and Ear Boston Massachusetts 02114 Recruiting
Ophthalmic Consultants of Boston Boston Massachusetts 02114 Recruiting
University of Michigan Health - Kellogg Eye Center Ann Arbor Michigan 48105 Not yet recruiting
Midwest Vision Research Foundation Chesterfield Missouri 63017 Recruiting
NYU Langone Eye Center (Ophthalmology) New York New York 10017 Not yet recruiting
Duke Eye Center - Ophthalmology Durham North Carolina 27705 Not yet recruiting
Vance Thompson Vision - Sioux Falls Sioux Falls South Dakota 57108 Recruiting
Houston Eye Associates (HEA) Houston Texas 77030 Recruiting
The Eye Institute of Utah Salt Lake City Utah 84107 Recruiting
Virginia Eye Consultants Norfolk Virginia 23502 Recruiting

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 59 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07519902, 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 Jul 15, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07519902 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →