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GA News

๐†๐€ ๐๐ž๐ฐ๐ฌ

๐Ÿ‘€ ๐๐š๐ฎ๐ฌ๐œ๐ก + ๐‹๐จ๐ฆ๐› ๐€๐œ๐ช๐ฎ๐ข๐ซ๐ž๐ฌ ๐–๐ก๐ข๐ญ๐ž๐œ๐š๐ฉ ๐๐ข๐จ๐ฌ๐œ๐ข๐ž๐ง๐œ๐ž๐ฌ
Bausch + Lomb has announced the acquisition of Whitecap Biosciences, LLC, which is currently developing 2 therapies for potential use in glaucoma and geographic atrophy (GA). This acquisition aims to enhance Bausch + Lombโ€™s clinical-stage pipeline with innovative treatments targeting two of the leading causes of blindness in ophthalmology.

Yehia Hashad MD, MD, Chief Medical Officer and Executive Vice President of research & development at Bausch + Lomb, stated, โ€œGlaucoma and geographic atrophy are two areas where we believe that dramatic improvement is possible. Whitecap Biosciencesโ€™ investigational medicines show real promise when it comes to slowing vision loss and perhaps even improving vision for patients with glaucoma, which would be a long-overdue breakthrough.โ€

๐Ÿ‘€ ๐€๐ฏ๐ข๐œ๐ž๐๐š ๐’๐ž๐œ๐ฎ๐ซ๐ž๐ฌ $207.5๐Œ ๐ญ๐จ ๐€๐๐ฏ๐š๐ง๐œ๐ž ๐€๐•๐ƒ-104 ๐Ÿ๐จ๐ซ ๐†๐ž๐จ๐ ๐ซ๐š๐ฉ๐ก๐ข๐œ ๐€๐ญ๐ซ๐จ๐ฉ๐ก๐ฒ ๐“๐ซ๐ž๐š๐ญ๐ฆ๐ž๐ง๐ญ
Aviceda Therapeutics has successfully secured $207.5 million in Series C financing to support its ongoing Phase 2b and Phase 3 clinical trials of AVD-104 for geographic atrophy (GA).

The ongoing phase 2b/3 trial is evaluating the safety and efficacy of high and low dose AVD-104 compared to avacincaptad pegol (IZERVAY) in patients with GA. Enrolment for this study was completed in September 2024, and 12-month primary endpoint data is anticipated in the second half of 2025. With the backing of this investment, Aviceda is well-positioned to advance AVD-104 through pivotal clinical trials, bringing it closer to potential regulatory approval.