Monday, March 17, 2025

Eylea 8 mg Demonstrates Three-Year Safety and Efficacy in Wet AMD

Similar articles

Bayer and Regeneron have unveiled significant three-year results from the PULSAR study, confirming that Eylea™ 8 mg maintains its effectiveness and safety in treating wet age-related macular degeneration (nAMD). The open-label extension study showcased sustained visual acuity improvements and controlled retinal fluid levels, marking a promising advancement in nAMD treatment.

Table of Contents

Subscribe Weekly Market Access News

* indicates required

Sustained Visual Acuity and Extended Dosing Intervals

Patients receiving Eylea 8 mg continued to experience consistent gains in visual acuity over the three-year period. Notably, a substantial proportion of participants were able to extend their dosing intervals, with 40% maintaining a ≥5-month interval and 24% reaching up to six months. These extended intervals reduce the treatment burden on patients, enhancing their quality of life while maintaining therapeutic benefits.

Favorable Safety Profile Over Extended Period

The long-term safety of Eylea 8 mg remained robust, with no new adverse events emerging during the study. Rates of ocular treatment-related events were comparable across all treatment groups, and instances of intraocular inflammation remained low. This favorable safety profile underscores Eylea 8 mg’s suitability for long-term use in managing nAMD.

Inferences:

  • Eylea 8 mg offers a reliable treatment option with reduced frequency of injections.
  • The study supports the potential for Eylea 8 mg to become a new standard in nAMD care.
  • Extended dosing intervals can lead to improved patient adherence and satisfaction.

These findings not only reaffirm Eylea 8 mg’s role in managing nAMD but also highlight its capacity to lessen the treatment burden on patients. The ability to extend dosing intervals without compromising efficacy provides a significant advantage in patient care, potentially setting a new benchmark in retinal disease management.

Healthcare professionals can consider Eylea 8 mg as a viable long-term treatment strategy for nAMD, offering sustained visual benefits and enhanced safety. Patients stand to benefit from fewer injections and maintained vision, which can lead to a better overall quality of life. As the prevalence of nAMD continues to rise with an aging population, Eylea 8 mg presents a promising solution to meet this growing need.

Source


This article has been prepared with the assistance of AI and reviewed by an editor. For more details, please refer to our Terms and Conditions. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author.

Subscribe to our newsletter

To be updated with all the latest news, offers and special announcements.

Latest article