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Trial Match

Clinical trials test new treatments โ€” sometimes the newest options available for a disease. Find trials that are recruiting now, near you. Open one to see its eligibility rules as simple questions to go through with your doctor.

Know your stage or your test results (such as EGFR, HER2 or BRCA)? Match trials to your own profile - nothing you type is saved.

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10 recruiting trials

for Leber Hereditary Optic Disease

Gene Therapy Clinical Trial for the Treatment Of Leber's HereDitary Optic Neuropathy NCT04912843Phase 2, Phase 31 site๐Ÿ“ Beijing Wuhan Neurophth Biotechnology Limited Company ยท Tests: NR082 injection, Sham Injection Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford NCT01793168n/a1 site๐Ÿ“ Sioux Falls Sanford Health New Non-invasive Modalities for Assessing Retinal Structure and Function NCT03475173NA1 site๐Ÿ“ Iowa City Randy Kardon ยท Tests: LSFG-NAVI North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) NCT01694940n/a17 sites๐Ÿ“ San Diego๐Ÿ“ Stanford๐Ÿ“ Aurora Columbia University Efficacy and Safety Study of Bilateral IVT Injection of GS010 at Two Dose Levels in LHON Patients NCT07303296Phase 21 site๐Ÿ“ Paris GenSight Biologics ยท Tests: GS010 High dose, GS010 Low dose Stem Cell Ophthalmology Treatment Study II NCT03011541NA4 sites๐Ÿ“ Westport๐Ÿ“ Coral Springs๐Ÿ“ Vienna MD Stem Cells ยท Tests: Arm 1 Study to Evaluate Sepofarsen in Subjects With Leber Congenital Amaurosis (LCA) Type 10 (HYPERION) NCT06891443Phase 318 sites๐Ÿ“ San Francisco๐Ÿ“ Miami๐Ÿ“ Iowa City Laboratoires Thea ยท Tests: sepofarsen, Placebo IVT Metabolomics Analysis According to the Retinal Nerve Fiber Layer in Patients With NOHL Mutations (MรฉtabOCT) NCT06682819NA1 site๐Ÿ“ Paris Hรดpital Necker-Enfants Malades ยท Tests: Optical coherent tomography Safety and Tolerability of Subretinal OPGx-RDH12-1001 for LCA-Associated Inherited Retinal Degeneration (LCA-IRD) NCT07681778Phase 1, Phase 24 sites๐Ÿ“ Phoenix๐Ÿ“ Philadelphia๐Ÿ“ Dallas Opus Genetics, Inc ยท Tests: OPGx-RDH12 Inherited Retinal Degenerative Disease Registry NCT02435940n/a1 site๐Ÿ“ Columbia Foundation Fighting Blindness
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