11/09/2026
A landmark September for Hexiris. This fall, we’re bringing the OBi™ platform and our first in human clinical results to five major ophthalmology meetings across Europe and North America.
It starts today at the Ophthalmology Futures Forum in London, where co founder Dr. Nir Shoham Hazon presented Hexiris and our early clinical experience with OBi™ Core. From London to Ottawa, Halifax, and New Orleans, we’re putting our technology into the hands of ophthalmologists and continuing the conversation around a simple question:
Read the full press release here: https://www.globenewswire.com/news-release/2026/09/10/3359185/0/en/hexiris-ophthalmics-to-present-first-in-human-obi-glaucoma-data-at-five-fall-meetings-beginning-with-the-ophthalmology-futures-forum-in-london.html
𝘙𝘦𝘨𝘶𝘭𝘢𝘵𝘰𝘳𝘺 𝘴𝘵𝘢𝘵𝘶𝘴 𝘷𝘢𝘳𝘪𝘦𝘴 𝘣𝘺 𝘱𝘳𝘰𝘥𝘶𝘤𝘵 𝘢𝘯𝘥 𝘫𝘶𝘳𝘪𝘴𝘥𝘪𝘤𝘵𝘪𝘰𝘯. 𝘖𝘉𝘪™ 𝘊𝘰𝘳𝘦 𝘩𝘰𝘭𝘥𝘴 𝘢 𝘏𝘦𝘢𝘭𝘵𝘩 𝘊𝘢𝘯𝘢𝘥𝘢 𝘮𝘦𝘥𝘪𝘤𝘢𝘭 𝘥𝘦𝘷𝘪𝘤𝘦 𝘭𝘪𝘤𝘦𝘯𝘴𝘦 𝘢𝘯𝘥 𝘪𝘴 𝘍𝘋𝘈 𝘳𝘦𝘨𝘪𝘴𝘵𝘦𝘳𝘦𝘥. 𝘖𝘉𝘪™ 𝘎𝘰𝘯, 𝘖𝘉𝘪™ 𝘚𝘩𝘶𝘯𝘵, 𝘢𝘯𝘥 𝘖𝘉𝘪™ 𝘚𝘱𝘢𝘤𝘦𝘳 𝘢𝘳𝘦 𝘪𝘯𝘷𝘦𝘴𝘵𝘪𝘨𝘢𝘵𝘪𝘰𝘯𝘢𝘭 𝘢𝘯𝘥 𝘢𝘳𝘦 𝘯𝘰𝘵 𝘢𝘱𝘱𝘳𝘰𝘷𝘦𝘥 𝘧𝘰𝘳 𝘤𝘰𝘮𝘮𝘦𝘳𝘤𝘪𝘢𝘭 𝘶𝘴𝘦 𝘪𝘯 𝘵𝘩𝘦 𝘜𝘯𝘪𝘵𝘦𝘥 𝘚𝘵𝘢𝘵𝘦𝘴, 𝘊𝘢𝘯𝘢𝘥𝘢, 𝘰𝘳 𝘵𝘩𝘦 𝘌𝘶𝘳𝘰𝘱𝘦𝘢𝘯 𝘜𝘯𝘪𝘰𝘯, 𝘦𝘹𝘤𝘦𝘱𝘵 𝘸𝘩𝘦𝘳𝘦 𝘴𝘱𝘦𝘤𝘪𝘧𝘪𝘤𝘢𝘭𝘭𝘺 𝘢𝘶𝘵𝘩𝘰𝘳𝘪𝘻𝘦𝘥.