News

Article

Opthea Limited completes week 52 patient visits in the COAST trial

Author(s):

Key Takeaways

  • Opthea's COAST trial evaluates sozinibercept with aflibercept for wet AMD, aiming to show superiority over standard care.
  • Topline results for COAST are anticipated in early Q2 2025, with ShORe results expected mid-2025.
SHOW MORE

The topline results from the COAST trial is anticipated in early Q2 of 2025.

(Image Credit: AdobeStock/rogerphoto)

(Image Credit: AdobeStock/rogerphoto)

Opthea Limited has completed the final week 52 patient visit in the COAST trial, which is the first of two Phase 3 pivotal trials investigating the superiority and safety of sozinibercept in combination with aflibercept (COAST) or ranibizumab (ShORe), compared to standard of care alone for the treatment of wet AMD. The topline results from both trials are anticipated in early Q2 of 2025 (COAST) and mid 2025 (ShORe).

In a press release1 penned by Opthea, Frederic Guerard, PharmD, Chief Executive Officer of the company said, “The completion of the final week 52 patient visit in COAST is an important milestone in the development of sozinibercept, as we deliver on our mission of improving visual outcomes in patients with wet AMD to enable fuller and healthier lives. I would like to thank Charles Wykoff, MD, PhD as well as all of the COAST investigators and their clinical staff for their excellent work as we plan to announce the anticipated topline data in early Q2 CY25.”

Opthea is conducting 2 concurrent global pivotal Phase 3 clinical trials for the treatment of wet AMD, aiming to demonstrate superiority of sozinibercept combination therapy versus standard of care alone: COAST (Combination OPT-302 with Aflibercept Study) and ShORe (Study of OPT-302 in combination with Ranibizumab). The primary endpoint for both trials is the mean change in Best Corrected Visual Acuity (BCVA) from baseline to week 52 for sozinibercept combination therapy compared to anti-VEGF-A monotherapy.1

Beyond week 52, the company plans to have patients continue to be treated for an additional year to evaluate extended safety and tolerability up to a two-year period. Opthea’s Phase 3 program is designed to support a broad label and, if successful, enable sozinibercept to be approved for use in combination with any anti-VEGF-A therapy in wet AMD patients. Sozinibercept has received Fast Track Designation from the US FDA for the treatment of wet AMD.1

Reference:
  1. Opthea Completes COAST Final Week 52 Patient Visit. Opthea Limited. February 18, 2025. Accessed February 18, 2025. https://www.globenewswire.com/news-release/2025/02/18/3027661/0/en/Opthea-Completes-COAST-Final-Week-52-Patient-Visit.html
Related Videos
This series features 1 KOL.
This series features 1 KOL.
© 2025 MJH Life Sciences

All rights reserved.