
New mechanism of disease discovered for Retinitis Pigmentosa
The team have found the cause of disease in the first ever family tree drawn up at Moorfields Eye Hospital over 35 years ago, which had remained unsolved until now.
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The team have found the cause of disease in the first ever family tree drawn up at Moorfields Eye Hospital over 35 years ago, which had remained unsolved until now.
Biotechnology company ProQR has announced that two of its RNA therapy development programmes for inherited sight loss are being acquired by Laboratoires Théa, a company specialising in eye care products.
Formal notice of the forthcoming Annual General Meeting in July 2025.
Formal notice of the forthcoming Annual General Meeting in September 2024.
This year the AGM will be held on Saturday, 9 July at 4.00pm:
Formal notice of the forthcoming Annual General Meeting in June 2023.
There are many ongoing clinical and laboratory studies around the world, exploring innovative approaches to treating inherited sight loss.
Thursday 24 July 2025, 7.00pm - 8.00pm - via Zoom - Come and join Richard & Rachael for our latest meeting to hear from our guest speaker and experienced V.I world traveller, Emily Bartell.
Sepul Bio begins clinical trial of ultevursen for USH2A-associated RP