Study of AR-14034 in Participants with Neovascular Age-Related Macular Degeneration (nAMD)

Description

The primary purpose of this study is to evaluate the safety and durability of single- and repeat administration of AR-14034 Sustained Release (SR) in subjects with neovascular age-related macular degeneration (nAMD).

Conditions

Neovascular Age-related Macular Degeneration (nAMD)

Study Overview

Study Details

Study overview

The primary purpose of this study is to evaluate the safety and durability of single- and repeat administration of AR-14034 Sustained Release (SR) in subjects with neovascular age-related macular degeneration (nAMD).

A Phase 1/2 Two-Stage Dose Escalation and Randomized Parallel-Group Study to Evaluate the Safety, Preliminary Treatment Effects, and Durability of AR-14034 Sustained Release Implant Compared to Intravitreal Anti-Vascular Endothelial Growth Factor Treatment in Participants with Neovascular Age-Related Macular Degeneration

Study of AR-14034 in Participants with Neovascular Age-Related Macular Degeneration (nAMD)

Condition
Neovascular Age-related Macular Degeneration (nAMD)
Intervention / Treatment

-

Contacts and Locations

Mountain View

Northern California Retina Vitreous Associates Medical Group, Mountain View, California, United States, 94040

Pensacola

Retina Specialty Institute, Pensacola, Florida, United States, 32503

Saint Petersburg

Retina Vitreous Associates of Florida, Saint Petersburg, Florida, United States, 33711

Philadelphia

MidAtlantic Retina Research, Philadelphia, Pennsylvania, United States, 19107

Abilene

Retina Research Institute of Texas, Abilene, Texas, United States, 79606

San Antonio

Medical Center Ophthalmology Associates, San Antonio, Texas, United States, 78240

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    50 Years to

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    Alcon Research,

    Director of Clinical Development, Alcon, STUDY_DIRECTOR, Aerie Pharmaceuticals

    Study Record Dates

    2027-03