Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

A Dose Ranging Study of OPT-302 With Ranibizumab in Neovascular (Wet) AMD

ClinicalTrials.gov ID: NCT03345082

Public ClinicalTrials.gov record NCT03345082. 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 30, 2026, 12:05 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 Dose-Ranging Study of Intravitreal OPT-302 in Combination With Ranibizumab, Compared With Ranibizumab Alone, in Participants With Neovascular Age-Related Macular Degeneration (Wet AMD)

Brief summary

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

A multicentre, randomised, parallel group, sham-controlled, double-masked, dose-ranging study, investigating two doses of OPT-302 in combination with ranibizumab compared with ranibizumab with sham, over six consecutive monthly dosing cycles in participants with neovascular (wet) AMD.

Study identification

NCT ID
NCT03345082
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Opthea Limited
Industry
Enrollment
366 participants

Conditions and interventions

Interventions

Biological · Other

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
Nov 6, 2017 (Actual)
Primary completion
May 14, 2019 (Actual)
Completion
May 14, 2019 (Actual)
Last update posted
Jan 12, 2021

2017 – 2019

United States locations

U.S. sites
55
U.S. states
21
U.S. cities
52
Facility City State ZIP Site status
Opthea Investigational Site Phoenix Arizona 85014 —
Opthea Investigational Site Phoenix Arizona 85020 —
Opthea Investigational Site Beverly Hills California 90211 —
Opthea Investigational Site Encino California 91436 —
Opthea Investigational Site Palm Desert California 92260 —
Opthea Investigational Site Redlands California 92374 —
Opthea Study Site Sacramento California 95819 —
Opthea Investigational Site Sacramento California 95841 —
Opthea Investigational Site San Diego California 94143 —
Opthea Investigational Site Santa Ana California 92705 —
Opthea Investigational Site Santa Barbara California 93103 —
Opthea Investigational Site Santa Maria California 93454 —
Opthea Investigational Site Colorado Springs Colorado 80909 —
Opthea Investigational Site Golden Colorado 80401 —
Opthea Investigational Site Boynton Beach Florida 33426 —
Opthea Investigational Site Fort Myers Florida 33907 —
Opthea Investigational Site Fort Myers Florida 33912 —
Opthea Investigational Site Melbourne Florida 32901 —
Opthea Investigational Site Pensacola Florida 32503 —
Opthea Investigational Site St. Petersburg Florida 33703 —
Opthea Investigational Site Tallahassee Florida 32308 —
Opthea Investigational Site Winter Haven Florida 33880 —
Opthea Investigational Site Augusta Georgia 30909 —
Opthea Investigational Site Shawnee Mission Kansas 66204 —
Opthea Investigational Site Wichita Kansas 67214 —
Opthea Investigational Site Paducah Kentucky 42001 —
Opthea Investigational Site Baltimore Maryland 21204 —
Opthea Investigational Site Grand Rapids Michigan 49546 —
Opthea Investigational Site Las Vegas Nevada 89144 —
Opthea Investigational Site Reno Nevada 89502 —
Opthea Investigational Site Edison New Jersey 08820 —
Opthea Investigational Site Teaneck New Jersey 07666 —
Opthea Investigational Site Albuquerque New Mexico 87109 —
Opthea Investigational Site Lynbrook New York 11563 —
Opthea Investigational Site Rochester New York 14620 —
Opthea Investigational Site Syracuse New York 13224 —
Opthea Investigational Site Asheville North Carolina 28803 —
Opthea Investigational Site Charlotte North Carolina 28210 —
Opthea Investigational Site Cleveland Ohio 44195 —
Opthea Investigational Site Columbus Ohio 43212 —
Opthea Investigational Site Portland Oregon 97239 —
Opthea Investigational Site Camp Hill Pennsylvania 17011 —
Opthea Investigational Site Kingston Pennsylvania 18704 —
Opthea Investigational Site Philadelphia Pennsylvania 19107 —
Opthea Investigational Site Ladson South Carolina 29456 —
Opthea Investigational Site West Columbia South Carolina 29169 —
Opthea Investigational Site Abilene Texas 79606 —
Opthea Investigational Site Austin Texas 78705 —
Opthea Investigational Site Houston Texas 77030 —
Opthea Investigational Site San Antonio Texas 78240 —
Opthea Investigational Site The Woodlands Texas 77384 —
Opthea Investigational Site Willow Park Texas 76087 —
Opthea Investigational Site Fairfax Virginia 22031 —
Opthea Investigational Site Virginia Beach Virginia 23462 —
Opthea Investigational Site Silverdale Washington 98383 —

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 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03345082, 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 Jan 12, 2021 · Synced Oct 30, 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 NCT03345082 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →