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C1 inhibitor deficiency

MONDO:0007361

Also known as: Quincke oedema, complement component 4, partial deficiency OF

45 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Hereditary disease (176) Immune system disorder (148) Inborn error of immunity (118) Immunodeficiency disease (54) Human disease (14) Complement deficiency (2) Disease of genetic or genomic mechanism (2) Classic complement early component deficiency (0) Disease by body system or component (0)
Trials to join now! 20 Not yet recruiting 7 Not yet finished but already full! 6 Completed 11 Terminated 1
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  • Could a daily pill stop hereditary angioedema attacks?

    Disease control Terminated

    This trial tests whether an experimental oral medication, deucrictibant, can reduce the number of swelling attacks in people with hereditary angioedema (HAE) types I and II. Participants take either a low or high dose of the drug or a placebo for 12 weeks, and then may continue o…

    Phase: PHASE2 • Sponsor: Pharvaris Netherlands B.V. • Aim: Disease control

    Last updated Aug 18, 2026 05:00 UTC

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