Decentrialz logo
  • HIPAA Compliant
  • ISO 27001 Certified
Find Trials
About UsContact
Become a Volunteer+1 877 705 1914

Status:

COMPLETED

A Study Assessing AR-13503 Implant in Subjects With nAMD or DME

Lead Sponsor:

Aerie Pharmaceuticals

Conditions:

Neovascular Age-related Macular Degeneration

Diabetic Macular Edema

Eligibility:

All Genders

18+ years

Phase:

PHASE1

Brief Summary

First-in-Human Study of the Safety of AR-13503 Sustained Release Intravitreal Implant in Subjects with Neovascular Age-Related Macular Degeneration (nAMD) and Subjects with Diabetic Macular Edema (DME...

Detailed Description

This is a first-in-human study conducted in 2 sequential stages; each stage is 24 weeks in duration. Subjects with nAMD and subjects with DME were evaluated in Stage 1. Subjects with DME will be evalu...

Eligibility Criteria

Inclusion

  • Inclusion Criteria for Subjects with Neovascular Age-Related Macular Degeneration (nAMD)
  • 50 years of age or older
  • Presence of active subfoveal or juxtafoveal Choroidal Neovascularization (CNV) (any subtype) with leakage affecting the fovea secondary to Age-Related Macular Degeneration (AMD)
  • Best Corrected Visual Acuity (BCVA) in the study eye at Baseline (Day 0):
  • Stage 1: between 65 and 10 Early Treatment Diabetic Retinopathy Study (ETDRS) letters (20/50 and 20/640 Snellen equivalent)
  • Able and willing to give signed informed consent and follow study instructions
  • Inclusion Criteria for Subjects with Diabetic Macular Edema (DME)
  • Subjects with Diabetic Macular Edema (DME) must meet all the following criteria to enter into the study:
  • 18 years of age or older
  • Type 1 or 2 diabetes mellitus with center-involved DME
  • BCVA in the study eye at Baseline (Day 0):
  • Stage 1: between 65 and 10 ETDRS letters (20/50 and 20/640 Snellen equivalent) Stage 2: between 70 and 20 ETDRS letters (20/40 and 20/400 Snellen equivalent)
  • Able and willing to give signed informed consent and follow study instructions
  • Exclusion Criteria for Subjects with Neovascular Age-Related Macular Degeneration (nAMD)
  • Ophthalmic:
  • Use of intravitreal aflibercept within 8 weeks, ranibizumab or bevacizumab within 6 weeks
  • History of vitreoretinal surgery in the study eye
  • Any ocular disease in the study eye that in the Investigator and Reading Center's opinion may confound assessment of the macula, affect central vision, confound results, or preclude improvement in visual acuity
  • Any current or history of periocular or intraocular inflammation or evidence of infection in either eye
  • Media clarity insufficient to obtain quality fundus and OCT images in the study eye
  • Systemic:
  • History or current systemic condition that in the Investigator opinion preclude the safe administration of the study treatment or confound results
  • History of allergy or sensitivity to fluorescein or povidone iodine
  • Women of childbearing potential who are pregnant, nursing, planning a pregnancy, or not using a medically acceptable form of birth control
  • Participation in an investigational study within 30 days of Screening
  • Exclusion Criteria for Subjects with DME
  • Ophthalmic:
  • Use of intraocular or periocular corticosteroids within 6 months, aflibercept within 8 weeks, ranibizumab or bevacizumab within 6 weeks
  • History of vitreoretinal surgery in the study eye
  • High risk proliferative diabetic retinopathy in the study eye and related complications
  • Structural damage to the center or the macula that is likely to preclude improvement in visual acuity in the study eye after resolution of the DME
  • Media clarity insufficient to obtain quality fundus and OCT images in the study eye
  • Systemic:
  • History or current medical condition that in the Investigator's opinion preclude the safe administration of the study treatment or confound results
  • History of allergy or sensitivity to fluorescein or povidone iodine
  • Women of childbearing potential who are pregnant, nursing, planning a pregnancy, or not using a medically acceptable form of birth control
  • Participation in an investigational study within 30 days of Screening

Exclusion

    Key Trial Info

    Start Date :

    June 24 2019

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    May 12 2022

    Estimated Enrollment :

    18 Patients enrolled

    Trial Details

    Trial ID

    NCT03835884

    Start Date

    June 24 2019

    End Date

    May 12 2022

    Last Update

    February 9 2023

    Active Locations (6)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 2 (6 locations)

    1

    Retinal Research Institute, LLC

    Gilbert, Arizona, United States, 85296

    2

    Retina-Vitreous Associates Medical Group

    Beverly Hills, California, United States, 90211

    3

    Bay Area Retina Associates

    Walnut Creek, California, United States, 94598

    4

    Sterling Vision, PC dba Oregon Retina

    Eugene, Oregon, United States, 97401