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Terminated Phase 3 Interventional

Efficacy and Safety Trial of Conbercept Intravitreal Injection for Neovascular AMD (PANDA-2)

ClinicalTrials.gov ID: NCT03630952

Public ClinicalTrials.gov record NCT03630952. 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, 11:43 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 Multicenter, Double-Masked, Randomized, Dose-Ranging Trial to Evaluate the Efficacy and Safety of Conbercept Intravitreal Injection in Subjects With Neovascular Age-Related Macular Degeneration (AMD) (PANDA-2)

Brief summary

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

The purpose of this clinical study is to evaluate the efficacy and safety of two different levels of conbercept intravitreal (IVT) injection as compared to the approved vascular endothelial growth factor (VEGF) antagonist active control, aflibercept intravitreal injection (2.0 mg/eye, Eylea®), in subjects with neovascular AMD.

Study identification

NCT ID
NCT03630952
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
1,157 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
Dec 21, 2018 (Actual)
Primary completion
Sep 10, 2020 (Actual)
Completion
May 19, 2021 (Actual)
Last update posted
Jun 23, 2021

2018 – 2021

United States locations

U.S. sites
69
U.S. states
29
U.S. cities
64
Facility City State ZIP Site status
Kanghong Investigative Site Phoenix Arizona 85020 —
Kanghong Investigative Site Phoenix Arizona 85021 —
Kanghong Investigative Site Springdale Arkansas 72762 —
Kanghong Investigative Site Arcadia California 91006 —
Kanghong Investigative Site Arcadia California 91007 —
Kanghong Investigative Site Bakersfield California 93309 —
Kanghong Investigative Site Encino California 91436 —
Kanghong Investigative Site Glendale California 91203 —
Kanghong Investigative Site Glendora California 91741 —
Kanghong Investigative Site Huntington Beach California 92647 —
Kanghong Investigative Site Pasadena California 91107 —
Kanghong Investigative Site Poway California 92064 —
Kanghong Investigative Site Redlands California 92373 —
Kanghong Investigative Site Redlands California 92374 —
Kanghong Investigative Site Riverside California 92505 —
Kanghong Investigative Site San Francisco California 94109 —
Kanghong Investigative Site Santa Barbara California 93013 —
Kanghong Investigative Site Colorado Springs Colorado 80909 —
Kanghong Investigative Site Waterford Connecticut 06385 —
Kanghong Investigative Site Boynton Beach Florida 33426 —
Kanghong Investigative Site Bradenton Florida 34209 —
Kanghong Investigative Site Miami Florida 33126 —
Kanghong Investigative Site Miami Florida 33143 —
Kanghong Investigative Site Stuart Florida 34994 —
Kanghong Investigative Site Winter Haven Florida 33880 —
Kanghong Investigative Site Atlanta Georgia 30328 —
Kanghong Investigative Site Augusta Georgia 30909 —
Kanghong Investigative Site Marietta Georgia 30060 —
Kanghong Investigative Site Elmhurst Illinois 60126 —
Kanghong Investigative Site Indianapolis Indiana 46290 —
Kanghong Investigative Site New Albany Indiana 47150 —
Kanghong Investigative Site Leawood Kansas 66211 —
Kanghong Investigative Site Springfield Massachusetts 01107 —
Kanghong Investigative Site Grand Rapids Michigan 49546 —
Kanghong Investigative Site Traverse City Michigan 49686 —
Kanghong Investigative Site St Louis Missouri 63128 —
Kanghong Investigative Site Reno Nevada 89502 —
Kanghong Investigative Site Northfield New Jersey 08205 —
Kanghong Investigative Site Teaneck New Jersey 07666 —
Kanghong Investigative Site Albuquerque New Mexico 87109 —
Kanghong Investigative Site Brooklyn New York 11201 —
Kanghong Investigative Site Great Neck New York 11021 —
Kanghong Investigative Site Liverpool New York 13088 —
Kanghong Investigative Site Shirley New York 11967 —
Kanghong Investigative Site Asheville North Carolina 28803 —
Kanghong Investigative Site Winston-Salem North Carolina 27157 —
Kanghong Investigative Site Youngstown Ohio 44505 —
Kanghong Investigative Site Oklahoma City Oklahoma 73104 —
Kanghong Investigative Site Medford Oregon 97504 —
Kanghong Investigative Site Portland Oregon 97225 —
Kanghong Investigative Site Springfield Oregon 97477 —
Kanghong Investigative Site Camp Hill Pennsylvania 17011 —
Kanghong Investigative Site Kingston Pennsylvania 18704 —
Kanghong Investigative Site Ladson South Carolina 29456 —
Kanghong Investigative Site Rapid City South Dakota 57701 —
Kanghong Investigative Site Arlington Texas 76012 —
Kanghong Investigative Site Austin Texas 78705 —
Kanghong Investigative Site Austin Texas 78731 —
Kanghong Investigative Site Bellaire Texas 77401 —
Kanghong Investigative Site Dallas Texas 75231 —
Kanghong Investigative Site Fort Worth Texas 76102 —
Kanghong Investigative Site Kingwood Texas 77339 —
Kanghong Investigative Site McAllen Texas 78503 —
Kanghong Investigative Site Midland Texas 79706 —
Kanghong Investigative Site Temple Texas 76502 —
Kanghong Investigative Site Salt Lake City Utah 84107 —
Kanghong Investigative Site Burlington Vermont 05401 —
Kanghong Investigative Site Charlottesville Virginia 22903 —
Kanghong Investigative Site Bellevue Washington 98004 —

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 85 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03630952, 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 Jun 23, 2021 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03630952 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →