Viewing Study NCT05040256


Ignite Creation Date: 2025-12-24 @ 11:35 PM
Ignite Modification Date: 2026-01-02 @ 4:14 AM
Study NCT ID: NCT05040256
Status: COMPLETED
Last Update Posted: 2021-11-15
First Post: 2021-05-11
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Neurologic and Immunologic Characteristics of CTLA-4 and LRBA Hereditary Deficiency
Sponsor: University Hospital, Montpellier
Organization:

Study Overview

Official Title: Neurologic and Immunologic Characteristics of CTLA-4 and LRBA Hereditary Deficiency
Status: COMPLETED
Status Verified Date: 2021-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: CTLA4 and LRBA deficiencies are rare genetic disorders, recently described, and associated with multiple clinical features. It ranges from recurrent infections, auto-immunity, and organ infiltration with lymphocytes. Neurologic syndroms are described in up to 30% of patients, yet they are poorly defined to date. Early recognition of a specific pattern can be important, given that there is a targeted therapy in this situation.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: