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Autosomal recessive congenital ichthyosis 7

MONDO:0014009

An autosomal recessive congenital ichthyosis characterized by fine whitish scales, moderate to severe erythroderma, compact hyperkeratosis, hypergranulosis, acanthosis, and papillomatosis that has material basis in variation in the chromosome region 12p11.2-q13.1.

Also known as: ARCI7, autosomal recessive congenital ichthyosis type 7, ichthyosis, congenital, autosomal recessive 7

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

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Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Ichthyosis (11) Hereditary skin disorder (5) Inherited ichthyosis (5) Autosomal recessive disease (4) Disease of genetic or genomic mechanism (2) Autosomal recessive congenital ichthyosis (1)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 2 Completed 2 Terminated 1
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  • Promising ichthyosis drug trial stalls after just 5 patients

    Disease control Terminated

    This study tested a drug called imsidolimab (ANB019) in people with ichthyosis, a condition that causes dry, scaly, and red skin. The trial aimed to see if the drug could improve skin symptoms compared to a placebo. However, the study was stopped early and only enrolled 5 partici…

    Phase: PHASE2 • Sponsor: Vanda Pharmaceuticals • Aim: Disease control

    Last updated Jun 26, 2026 17:50 UTC

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