Viewing StudyNCT06435000



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06435000
Status: RECRUITING
Last Update Posted: 2024-07-03
First Post: 2024-05-24

Brief Title: An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 STGD1 Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene
Sponsor:
Organization: Splice Bio

Study Design

Study Type: OBSERVATIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: False
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: SAMPLES_WITH_DNA
Bio Spec Description: Buccal saliva swab to determine a minimum of two pathogenic or likely pathogenic mutations in the ABCA4 gene to genetically confirm the disease as per eligibility criteria
Enrollment Count: 75
Enrollment Type: ESTIMATED
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
Name
Cohort
Time Perspective List:

Clinical Trial Statuses

Name
107271
Who Masked List: