Gene Data From HGNC: https://www.genenames.org/download/statistics-and-files/
Symbol:
CEP290
Name:
centrosomal protein 290
Location:
12q21.32
Locus Group:
protein-coding gene
Gene Type:
Protein Coding
Locus Type:
gene with protein product
Clinical Trials Data: https://classic.clinicaltrials.gov/api/gui/ref/download_all
Clinical Studies
| NCT Number | Status | Brief Title | View |
|---|---|---|---|
| NCT00873678 | Assessment of the Prevalence of Genes AHI1 NPHP1 and CEP290 in Joubert Syndrome | View | |
| NCT03872479 | Single Ascending Dose Study in Participants With LCA10 | View | |
| NCT03140969 | Study to Evaluate QR-110 in Lebers Congenital Amaurosis LCA Due to the c29911655AG Mutation pCys998X in the CEP290 Gene | View | |
| NCT05203939 | Study to Assess the Safety and Efficacy of OCU400 for Retinitis Pigmentosa and Leber Congenital Amaurosis | View | |
| NCT03913130 | Extension Study to Study PQ-110-001 NCT03140969 | View | |
| NCT04855045 | An Open-label Dose Escalation and Double-masked Randomized Controlled Trial Evaluating Safety and Tolerability of Sepofarsen in Children 8 Years of Age With LCA10 Caused by Mutations in the CEP290 Gene | View | |
| NCT03396042 | Natural History Study of CEP290-Related Retinal Degeneration | View | |
| NCT03913143 | A Study to Evaluate Efficacy Safety Tolerability and Exposure After a Repeat-dose of Sepofarsen QR-110 in LCA10 ILLUMINATE | View |