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:
Organization: ProQR Therapeutics

Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 11
Enrollment Type: ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Name
PHASE1
PHASE2
Observational Models:
Time Perspective List:
Who Masked List: