Clin2
NCT07653971Possibly a fitNot yet recruiting

Gene therapy for Bietti's crystalline dystrophy

Bietti's Crystalline DystrophyBietti Crystalline Corneoretinal Dystrophy

Part of Eyes & vision clinical trials.

This trial tests a new gene therapy for Bietti's crystalline dystrophy, a rare inherited eye disease that causes progressive vision loss. The treatment aims to slow or stop vision loss by delivering a healthy gene to the eye.

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

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

Who can take part

  • You must be at least 18 years old.
  • You must have a confirmed diagnosis of Bietti's crystalline dystrophy (BCD), a rare inherited eye condition.
  • You must have genetic testing showing you have a mutation in the CYP4V2 gene.
  • Your vision in the study eye must be significantly reduced, around 20/100 or worse.
  • You must not have had gene therapy or stem cell therapy for BCD in the study eye.

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.

Similar studies

Other trials that look related to this one.

NCT07307469Enrolling by invitation
Extended access to ZVS101e for BCD patients

This trial offers compassionate use of the gene therapy ZVS101e for people with Bietti crystalline dystrophy (BCD) who were in the control group of an earlier study. It aims to give extended treatment access to those who didn't receive the experimental therapy before.

Beijing, Beijing Municipality
NCT07586306Not yet recruiting· Phase 1/Phase 2
Safety study of second eye treatment for Bietti's crystalline dystrophy

This study tests the safety of giving the same gene therapy to your second eye, after you already received it in one eye during an earlier study. It aims to see if it's safe and may help improve vision.

Beijing, Beijing Municipality
NCT07269665Recruiting· Early Phase 1
Gene therapy trial for children with BBS1 retinal degeneration

This early-phase trial tests a gene therapy called AXV-101 for children with vision loss caused by BBS1 genetic mutations. The goal is to see if it can help slow or stop retinal damage.

London
NCT07241169Recruiting· Early Phase 1
Gene therapy trial for ABCA4-related retinal disease

This trial tests a new gene therapy called ZVS106e for people with inherited retinal degeneration caused by changes in both copies of the ABCA4 gene. The therapy aims to slow or stop vision loss, and the study will check if it is safe and if it works.

Beijing, Beijing Municipality
NCT07002398Recruiting· Phase 1/Phase 2
Gene therapy for Stargardt disease (VG801)

This trial tests a new gene therapy called VG801 for people with Stargardt disease, a genetic condition that causes vision loss. The treatment aims to improve or slow vision loss by delivering a working copy of the ABCA4 gene to the retina.

Shanghai, Shanghai Municipality
NCT07185256Recruiting· Phase 1/Phase 2
Gene therapy for Best disease retinal trial

This trial tests a gene therapy called OPGx-BEST1 injected under the retina to treat vision loss from Best vitelliform macular dystrophy or a related condition. It may help people with advanced disease who have a specific genetic change in the BEST1 gene.

Los Angeles, California

Hear when a new Bietti's Crystalline Dystrophy trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.