Viewing Study NCT05833620


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Study NCT ID: NCT05833620
Status: NOT_YET_RECRUITING
Last Update Posted: 2023-04-27
First Post: 2023-03-17
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Identification and Characterization of Genetic Variants in Hereditary Angioedema
Sponsor: Hospital Universitari Vall d'Hebron Research Institute
Organization:

Study Overview

Official Title: Identification and Functional Characterization of Genetic Variants Associated With Specific Clinical Phenotypes in Hereditary Angioedema Due to C1 Inhibitor Deficiency: An Unbiased Approach
Status: NOT_YET_RECRUITING
Status Verified Date: 2023-04
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: GENOMAEH_01
Brief Summary: This project aims to analyse in an unbiased way the existence of genetic variants that contribute to explaining and predicting the differences in clinical expression between patients with HAE.
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?: