Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional

A Multicenter, Randomized, Double-Masked, Placebo-Controlled Pilot Study to Evaluate the Efficacy and Safety of ZOC2017217 in Subjects With Age-Related Cataract

ClinicalTrials.gov ID: NCT07395986

Public ClinicalTrials.gov record NCT07395986. 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 Oct 20, 2026, 3:11 PM EDT

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

Brief summary

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

This is a multicenter, randomized, double-masked, placebo-controlled pilot study conducted in the United States (US) in subjects with age-related cataract in one or both eyes. Approximately 40 subjects with age-related cataract will be stratified by race and Best Corrected Distance Visual Acuity (BCDVA) and randomized (1:1) to active investigational product (IP) or placebo. Subjects will administer their assigned IP in both eyes, except as noted below, two times a day (BID) for 24 weeks before being exited from the study. Subjects with new or ongoing ocular adverse events (AEs) at the time of planned study exit will be asked to return 2 weeks later for a safety follow-up evaluation. The study eye will be the qualified eye that meets study eligibility criteria. Data from the study eye will be used for the purposes of efficacy analyses. Both eyes will receive treatment, except in subjects who have previously undergone cataract surgery in the non-study eye or whose non-study eye, in the opinion of the Investigator, is not suitable for treatment with the IP due to safety or another concern.

Study identification

NCT ID
NCT07395986
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
8 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
50 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
Feb 10, 2026 (Actual)
Primary completion
Feb 2027 (Estimated)
Completion
Feb 2027 (Estimated)
Last update posted
Aug 11, 2026

2026 – 2027

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
21
Facility City State ZIP Site status
Cornea and Cataract Consultants of Arizona Scottsdale Arizona 85255 —
Catalina Eye Tucson Arizona 85712 —
Global Research Management Glendale California 91204 —
Inland Eye Specialists Hemet California 92545 —
United Medical Research Institute Inglewood California 90301 —
North Bay Eye Associates, Inc. Petaluma California 94954 —
East West Eye Institute - Torrance Torrance California 90505 —
ICON Eye Care Grand Junction Colorado 81501 —
Advanced Vision Research Institute Longmont Colorado 80503 —
Rand Eye Institute Deerfield Beach Florida 33064 —
Levenson Eye Associates Jacksonville Florida 32204 —
Clayton Eye Clinical Research, LLC Morrow Georgia 30260 —
Springfield Clinic Springfield Illinois 62703 —
Oculus Research - Cary Cary North Carolina 27518 —
Bergstrom Eye Research Fargo North Dakota 58103 —
Cincinnati Eye Institute - Blue Ash Blue Ash Ohio 45242 —
Verum Research Eugene Oregon 97401 —
Erie Retina Research Erie Pennsylvania 16505 —
Valley Retina Institute P.A. Laredo Texas 78041 —
Valley Retina Institute P.A. McAllen Texas 78503 —
R and R Eye Research, LLC San Antonio Texas 78229 —

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 NCT07395986, 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 Aug 11, 2026 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07395986 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →