Clin2
NCT06445322Possibly a fitRecruiting

Finding people with Stargardt disease for ACDN-01

Stargardt DiseaseStargardt Disease 1Cone Rod DystrophyJuvenile Macular Degeneration

Part of Eyes & vision, Genetic & congenital clinical trials.

This prescreening study looks for people with a specific genetic eye condition called Stargardt disease to see if they might be able to join a future trial for a new treatment called ACDN-01.

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

Phase
N/A
Enrollment
50 people
Ages
5 years and older
Study type
Observational

Who can take part

  • You have a confirmed change (mutation) in the ABCA4 gene.
  • You have been diagnosed with Stargardt disease type 1 or cone-rod dystrophy (a related eye condition).
  • You do not have other harmful gene changes that cause similar eye diseases.
  • You do not have other serious eye conditions besides ABCA4-related disease.
  • You do not have any other medical or mental health conditions that would make it unsafe or difficult to join the study.

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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