Viewing StudyNCT03140969



Ignite Creation Date: 2024-05-06 @ 10:01 AM
Last Modification Date: 2024-10-26 @ 12:23 PM
Study NCT ID: NCT03140969
Status: COMPLETED
Last Update Posted: 2022-12-27
First Post: 2017-05-01

Brief Title: Study to Evaluate QR-110 in Lebers Congenital Amaurosis LCA Due to the c29911655AG Mutation pCys998X in the CEP290 Gene
Sponsor: ProQR Therapeutics
Organization: ProQR Therapeutics

Conditions & Keywords Data

Conditions:
Name
Lebers Congenital Amaurosis
Keywords:
Name View
Lebers congenital amaurosis View
CEP290 View
pCys998X View
c29911655AG View
RNA therapy View
Antisense oligonucleotide View