Clin2
NCT06789445Worth exploringRecruiting

Cell therapy for inherited retinal disease (CLARICO)

Primary Photoreceptor DiseaseRetinitis Pigmentosa (RP)Usher SyndromeInherited Retinal Disease (IRD)Rod-Cone DystrophyRod-Cone DiseaseRetinal DegenerationCone-Rod Disease (C-RD)

Part of Brain & nervous system, Ear, nose & throat, Eyes & vision, Genetic & congenital clinical trials.

This study tests a new cell therapy (OpCT-001) for adults with inherited retinal diseases that affect the light-sensing cells. It aims to see if the treatment is safe and possibly helps improve vision.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
54 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have a confirmed genetic diagnosis of a primary photoreceptor disease (a type of inherited eye condition that affects the light-sensing cells in your retina).
  • Your vision in the study eye must fall within a specific range: for Phase 1, between counting fingers and 20/40; for Phase 2, between 20/25 and 20/60 on an eye chart.
  • Your retina must have areas that are suitable for the study treatment to be injected.
  • You cannot have active eye inflammation, infection, glaucoma, diabetic eye disease, or significant macular edema.
  • You cannot have had any prior cell therapy, gene therapy, retinal implant, or organ transplant.
  • You must not have had eye surgery in the last 3 months or have a current or recent (within 5 years) cancer (except treated basal cell skin cancer).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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