Clin2
NCT07796646Possibly a fitNot yet recruiting

Long-term safety of ultevursen for retinitis pigmentosa

Retinitis Pigmentosa (RP)Usher Syndrome Type 2Deaf BlindRetinal DiseaseEye Diseases, HereditaryEye Disorders CongenitalVision Disorders

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

This study checks the long-term safety of a medicine called ultevursen for people with retinitis pigmentosa caused by changes in a specific gene. It is for people who have already finished the earlier LUNA study and might continue treatment or just be followed for observation.

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

Phase
Phase 2
Enrollment
81 people
Ages
8 years and older
Study type
Interventional

Who can take part

  • You must have completed the LUNA study through 24 months.
  • You must be at least 8 years old (minors need parent permission).
  • You must be willing to attend all study visits for 24 months.
  • If you are in the treatment group, you must not be pregnant or breastfeeding and must use effective birth control.
  • You must not have new eye problems or allergies that make the injection unsafe.

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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