Bausch + Lomb reports 24-month U.S. ELIOS glaucoma trial results with 76% achieving ≥20% IOP reduction

Reuters03-23
Bausch + Lomb reports 24-month U.S. ELIOS glaucoma trial results with 76% achieving ≥20% IOP reduction
  • Bausch + Lomb reported positive 24-month results from a pivotal U.S. clinical trial of the ELIOS System, an implant-free excimer laser procedure intended to reduce elevated intraocular pressure in open-angle glaucoma.
  • The prospective, multicenter study enrolled 318 patients at 20 U.S. sites who had mild to moderate primary open-angle glaucoma and cataracts.
  • Unmedicated diurnal intraocular pressure was reduced by at least 20% in 76% of patients, and the average decrease was 7.4 mmHg.
  • At 23 months, 82% of patients were medication-free, and no intraoperative complications were reported.
  • Topline results were scheduled to be discussed during a company R&D webinar, and detailed results were slated for submission to a future medical meeting and a peer-reviewed journal.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Bausch + Lomb Corp. published the original content used to generate this news brief via Business Wire (Ref. ID: 20260323739970) on March 23, 2026, and is solely responsible for the information contained therein.

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