Viewing Study NCT05040256



Ignite Creation Date: 2024-05-06 @ 4:39 PM
Last Modification Date: 2024-10-26 @ 2:13 PM
Study NCT ID: NCT05040256
Status: COMPLETED
Last Update Posted: 2021-11-15
First Post: 2021-05-11

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

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: None
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?: None