Gene Therapy for Autosomal Recessive RP Caused by MERTK Mutations
|
Description: This Phase I clinical trial is evaluating the safety of gene replacement therapy for people with retinitis pigmentosa (RP) caused by mutations in the gene MERTK. Efficacy is being evaluated, as well. Initially, 6 participants (children and young adults) will receive a single subretinal injection of the treatment in one eye. The treatment consists of a corrective MERTK gene, which is delivered to retinal pigment epithelial (RPE) cells by an adeno-associated virus (AAV), a therapeutic man-made virus.
Clinical Contacts: |














![Casting A Wide Net[work] | Presenting the interactive Foundation Fighting Blindness 2012 Annual Report 2012 Annual Report banner](https://www.blindness.org/images/banners/annual_report_box.jpg)


