Eye disease study paves way for gene therapy breakthrough
NCT ID NCT04639635
First seen Jan 11, 2026 · Last updated May 15, 2026 · Updated 22 times
Summary
This study looks at a rare genetic eye disease called CNGB1 retinitis pigmentosa, which causes gradual vision loss and blindness. Researchers will follow 20 people over 3 years using eye exams and imaging to track how the disease progresses. The goal is to find the best ways to measure the disease so that future gene therapy trials can test treatments effectively. No treatment is given in this study.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Dr. Stephen H. Tsang
New York, New York, 10032, United States
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Eberhard Karls University Tubingen
Tübingen, Germany
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Institut de la Vision/Centre de maladies rares du Centre Hospitalier National Ophtalmologique des Quinze-Vingts
Paris, France
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Klinikum der Universität München University Eye Hospital, Ludwig-Maximilians-University (LMU) Munich
München, Bavaria, 80336, Germany
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Moorfields Eye Hospital NHS Foundation Trust
London, United Kingdom
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Wills Eye Hospital
Philadelphia, Pennsylvania, 19107, United States
Conditions
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