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Hypercholesterolemia, autosomal dominant, 3

MONDO:0011369

Any familial hypercholesterolemia in which the cause of the disease is a mutation in the PCSK9 gene.

Also known as: PCSK9 familial hypercholesterolemia, familial hypercholesterolemia caused by mutation in PCSK9, hypercholesterolemia, autosomal dominant, 3, hypercholesterolemia, autosomal dominant, type 3, hypercholesterolemia, familial, 3, low density lipoprotein cholesterol level QTL 1, Fh3, HCHOLA3

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

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Broader categories

Disease (680) Hyperlipidemia (295) Metabolic disease (233) Inherited lipid metabolism disorder (189) Hereditary disease (176) Familial hypercholesterolemia (56) Inborn errors of metabolism (45) Human disease (14) Familial hyperlipidemia (8) Hyperlipoproteinemia (8)
Trials to join now! 2 Not yet finished but already full! 1 Completed 1
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  • New drug interaction study completed: no treatment, just data

    Knowledge-focused Completed

    This study looked at how an experimental drug called AZD0780 affects the way the body processes metformin, a common diabetes medicine. Fourteen healthy volunteers took both drugs, and researchers measured drug levels in the blood. The goal was purely to gather information on drug…

    Phase: PHASE1 • Sponsor: AstraZeneca • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:09 UTC

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