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Meiragtx Uk Ii Ltd

Clinical trials sponsored by Meiragtx Uk Ii Ltd, explained in plain language.

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  • Mapping the slow fade of RPE65 blindness to speed future cures

    Knowledge-focused Completed

    Researchers are following people with Leber congenital amaurosis caused by RPE65 gene mutations to see how their vision and retinas change over time. The study enrolls children and adults, ages 3 and older, who have this inherited retinal dystrophy. Participants undergo regular e…

    Sponsor: MeiraGTx UK II Ltd • Aim: Knowledge-focused

    Last updated Sep 21, 2026 19:00 UTC

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