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Terminated Phase 2 Interventional Results available

X-82 to Treat Age-related Macular Degeneration

ClinicalTrials.gov ID: NCT02348359

Public ClinicalTrials.gov record NCT02348359. 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 6, 2026, 9:27 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 Randomized, Double-Masked, Placebo-Controlled, Dose- Finding, Non-Inferiority Study of X-82 Plus Prn Intravitreal (Ivt) Anti-VEGF Compared to Prn Ivt Anti-VEGF Monotherapy in Neovascular AMD

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of X-82 in the treatment of vision loss due to wet AMD.

Study identification

NCT ID
NCT02348359
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Tyrogenex
Industry
Enrollment
157 participants

Conditions and interventions

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
Mar 15, 2015
Primary completion
Dec 11, 2017
Completion
Jan 11, 2018
Last update posted
Feb 10, 2022

2015 – 2018

United States locations

U.S. sites
35
U.S. states
18
U.S. cities
35
Facility City State ZIP Site status
Not listed Tucson Arizona
Not listed Beverly Hills California
Not listed Huntington Beach California
Not listed Redlands California
Not listed Sacramento California
Not listed Colorado Springs Colorado
Not listed Golden Colorado
Not listed New London Connecticut
Not listed Fort Myers Florida
Not listed Lakeland Florida
Not listed Melbourne Florida
Not listed Miami Florida
Not listed Palm Beach Gardens Florida
Not listed Augusta Georgia
Not listed Lemont Illinois
Not listed Oak Forest Illinois
Not listed Indianapolis Indiana
Not listed Baltimore Maryland
Not listed Glen Burnie Maryland
Not listed Boston Massachusetts
Not listed Springfield Massachusetts
Not listed Portsmouth New Hampshire
Not listed Bloomfield New Jersey
Not listed Albany New York
Not listed New York New York
Not listed Asheville North Carolina
Not listed Charlotte North Carolina
Not listed Cleveland Ohio
Not listed Youngstown Ohio
Not listed Nashville Tennessee
Not listed Abilene Texas
Not listed Austin Texas
Not listed Houston Texas
Not listed The Woodlands Texas
Not listed Richmond Virginia

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 NCT02348359, 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 Feb 10, 2022 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02348359 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →