Retina360: Advances in the Management of Neovascular AMD and Sustained Drug Delivery for Retinal Diseases

1.75 CME
105 MINS
$0 FEE
SAVE
Retina360: Advances in the Management of Neovascular AMD and Sustained Drug Delivery for Retinal Diseases

Overview


Provider Statement

This continuing education activity is provided by Vindico Medical Education


Support Statement

This activity is supported by independent medical education grants from Regeneron Pharmaceuticals, Inc.; Astellas; Alimera Sciences, Inc.; Ocular Therapeutix, Inc.; Outlook Therapeutics; and REGENXBIO Inc.


Activity Description

The continued evolution of treatment protocols and imaging modalities for the management of retinal diseases offers the potential to further optimize visual and anatomical outcomes for patients with these diseases. Furthermore, with the addition of newly approved therapies that have longer durations of action, sustained drug delivery systems, and emerging novel therapies, it can be challenging to stay abreast of the numerous and ongoing therapeutic advances. In this CE activity, experts in the field review innovations in imaging that can improve the diagnosis and monitoring of neovascular age-related macular degeneration (nAMD) and evaluate the latest updates in therapeutic regimens for the optimal long-term management of these patients. In addition, they will evaluate the safety and efficacy of currently available and emerging sustained delivery platforms for the management of patients with nAMD and diabetic macular edema (DME).


Target Audience

The intended audience for this activity is US-based retina specialists and ophthalmologists involved in the management of patients with retinal diseases.


Learning Objectives

Upon successful completion of this educational activity, participants should be better able to:

  • Integrate the latest information about advances in imaging and treatment into practice to improve the management of patients with nAMD.
  • Summarize innovations in imaging that can improve the diagnosis and management of retinal diseases.
  • Describe current evidence about the safety and efficacy of sustained delivery platforms in the management of patients with nAMD and DME.

Activity Chair

Rishi P. Singh, MD
Staff Physician and President
Cleveland Clinic Martin Hospitals
Stuart, FL
Professor of Ophthalmology
Lerner College of Medicine
Case Western Reserve University
Cleveland, OH


Faculty

Margaret A. Chang, MD, MS
Senior Partner
Retinal Consultants of Sacramento
Sacramento, CA

Judy E. Kim, MD, FARVO, FASRS
Jean and Tom Walter Distinguished Chair of Ophthalmology
in Honor of James P. McCulley, MD
Vice Chair of Education
Medical Director of Clinical Research
University of Texas Southwestern Medical Center
Dallas, TX

Yasha Modi, MD
Associate Professor of Ophthalmology
New York University
New York, NY

Carl D. Regillo, MD, FACS
Director, Retina Service
Wills Eye Hospital
Professor of Ophthalmology
Thomas Jefferson University
Mid Atlantic Retina
Philadelphia, PA

Planner/Reviewer

Ronald A. Codario, MD, EMBA, FACP, FNLA, RPVI, CHCP


Accreditation

ACCME Jointly accredited In support of improving patient care, Vindico Medical Education is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.


Credit Designation

Vindico Medical Education designates this enduring material for a maximum of 1.75 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

This enduring material is approved for 1 year from the date of original release, January 31, 2025, to January 30, 2026.


How to Participate in This Activity and Obtain CE Credit

To participate in this activity, you must read the objectives, answer the polling and pretest questions, view the content, and complete the posttest and evaluation. Provide only one (1) correct answer for each question. A satisfactory score is defined as answering 5 of the 7 posttest questions correctly. If a satisfactory score on the posttest is achieved, Vindico Medical Education will issue an AMA PRA Category 1 Credit(s)™ certificate.


Disclosures

Vindico Medical Education adheres to the ACCME’s Standards for Integrity and Independence in Accredited Continuing Education. Any individuals in a position to control the content of a continuing education activity, including faculty, planners, reviewers, or others, are required to disclose all relevant financial relationships with ineligible entities (commercial interests). All relevant conflicts of interest have been mitigated prior to the commencement of the activity.

Relationship information is accurate at the time of content development.

Activity Chair and Faculty report the following relevant financial relationship(s)

Margaret A. Chang, MD, MS
Consultant: AbbVie/Regenxbio, Astellas, EyePoint, Genentech, Ocular Therapeutix, Oculis, Zeiss
Speaker Contracted by Ineligible Company: Genentech
Independent Research Contractor: Alexion, Boehringer Ingelheim, EyeBio, Mylan, NGM, Novartis, OcuTerra, Outlook

Judy E. Kim, MD, FARVO, FASRS
Advisor: AbbVie, Amgen, Apellis, Bausch + Lomb, Clearside, DORC, EyePoint, Notal Vision, Regeneron
Consultant: Genentech/Roche, Notal Vision, Outlook Therapeutics

Yasha Modi, MD
Consultant: Alcon, Alimera, Allergan, Apellis, Astellas, DORC, EyePoint, Genentech, IVERIC bio, Neurotech, Notal Vision, Opthea, Regeneron, Thea, Zeiss

Carl D. Regillo, MD, FACS
Consultant: 4DMT, Adverum, Allergan, Annexon, Apellis, Astellas, Aviceda, Bausch + Lomb, BioCryst, Clearside, Cognition Therapeutics, Coherus, EyePoint, Genentech, IVERIC bio, Janssen, jCyte, Kodiak, Kyoto Drug Development, Lineage Cell Therapeutics, Merck, Neurotech, NGM Bio, Novartis, Novelty Nobility, Ocugen, Ocuphire, OcuTerra, Opthea, Outlook, Ray, Regeneron, Regenxbio, Sandoz, Stealth BioTherapeutics, Théa, Zeiss, Zip Bio
Independent Research Contractor: 4DMT, Adverum, Allergan, Annexon, Apellis, Astellas, EyePoint, Genentech, Gyroscope, IVERIC bio, Janssen, Kodiak, Lineage Cell Therapeutics, NGM Bio, Notal Vision, Novartis, Ocugen, OcuTerra, Opthea, Regeneron, Regenxbio
Stock Options: Aviceda, Ocugen

Rishi P. Singh, MD
Consultant: Alcon, Apellis, Bausch + Lomb, EyePoint, Genentech, IVERIC bio, Regenxbio, Regeneron, Zeiss
Independent Research Contractor: Janssen

Planner/Reviewer reports the following relevant financial relationship(s)

Ronald A. Codario, MD, EMBA, FACP, FNLA, RPVI, CHCP
No relevant financial relationships to disclose.

Vindico Medical Education staff report the following relevant financial relationship(s)

No relevant financial relationships to disclose.

Signed disclosures are on file at Vindico Medical Education, Office of Medical Affairs and Compliance.


Unlabeled and Investigational Usage

The audience is advised that this continuing education activity may contain references to unlabeled uses of FDA-approved products or to products not approved by the FDA for use in the United States. The faculty members have been made aware of their obligation to disclose such usage. All activity participants will be informed if any speakers/authors intend to discuss either non–FDA-approved or investigational use of products/devices.


Copyright Statement

Created and published by Vindico Medical Education, 6900 Grove Road, Building 100, Thorofare, NJ 08086-9447. Telephone: 856-994-9400; Fax: 856-384-6680. Printed in the USA. Copyright © 2025 Vindico Medical Education. All rights reserved. No part of this publication may be reproduced without written permission from the publisher. The material presented at or in any Vindico Medical Education continuing education activity does not necessarily reflect the views and opinions of Vindico Medical Education. Neither Vindico Medical Education nor the faculty endorse or recommend any techniques, commercial products, or manufacturers. The faculty/authors may discuss the use of materials and/or products that have not yet been approved by the FDA. All readers and continuing education participants should verify all information before treating patients or utilizing any product.


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CE Questions?

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