Usher 1F Collaborative
Usher 1F Collaborative
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Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Rate of Progression of PCDH15-Related Retinal Degeneration in Usher Syndrome 1F | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, autosomal recessive nonsyndromic hearing loss 23, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosa | Active, not recruiting | Not stated | 2026-02-04 | NCT04765345 |