Clin2
NCT06024057Possibly a fitNot yet recruiting

Extended study of gene therapy for inherited blindness

To Evaluate the Scaling Clinical Study of AAV2-RPE65 Gene Therapy Agent (LX101) in Patients With Congenital Amaurosis (LCA)

Part of Eyes & vision clinical trials.

This study is a long-term follow-up for people who already received a gene therapy (LX101) for a specific form of inherited blindness called LCA. The goal is to watch how they do over time and check for any lasting effects.

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

Phase
N/A
Enrollment
3 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You were already in the earlier LX101 gene therapy study for inherited blindness.
  • You and your guardian are willing to sign a consent form and commit to long-term follow-up visits.
  • You have no serious eye problems (like advanced glaucoma or cataracts) that could affect the treatment or study results.
  • You have no other health issues that make this study unsafe, such as an uncontrolled infection or recent surgery.
  • You are not pregnant, breastfeeding, or planning to become pregnant, and if you could become pregnant, you agree to use effective birth control.
  • You can stop taking certain medications (like sildenafil for erectile dysfunction or hydroxychloroquine) during 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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