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Hereditary Angioedema clinical trials

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NCT ID: NCT06467084 Not yet recruiting - Clinical trials for Hereditary Angioedema

Open-Label Safety, PK, and Efficacy Trial of Sebetralstat (KVD900) in Pediatric Patients (Ages 2-11) With HAE Type I or II

KONFIDENT-KID
Start date: June 24, 2024
Phase: Phase 3
Study type: Interventional

KVD900-303 is an open-label, multicenter clinical trial in patients aged 2 to 11 years old with HAE Type I or II.

NCT ID: NCT02159430 Not yet recruiting - Depression Clinical Trials

Hereditary AngioEdema, Neurobiology and Psychopathology

HAENP
Start date: November 2014
Phase: N/A
Study type: Observational [Patient Registry]

Since 1963 Hereditary AngioEdema (HAE) is considered an autosomal dominant disorder (Donaldson and Evans), characterized by a quantitative and/or qualitative deficit of C1 esterase inhibitor (C1-INH), which affects approximately 1:50.000 individuals in the general population. From this period the link between HAE and psychiatry was interrupted, however genetic issues could not comprehensively explain the clinical evolution of the disease. Clinical studies show an evident gap between genotype and phenotype of HAE. For this still controversial question, we have designed this cross-sectional study in order to establish the relationship between HAE clinical manifestations and neurobiological/psychopatological parameters.