Inherited ichthyosis
MONDO:0015947Mendelian disorders of cornification affecting all or most of integument characterized by hyperkeratosis and/or scaling, caused by an inherited modification of the individual's genome.
Also known as: congenital ichthyosis of skin, genetic ichthyosis, hereditary ichthyosis (disease), inherited genetic ichthyosis, congenital ichthyosis, fish scale disease, fish skin, ichthyosis congenita
33 clinical trials for this condition and its sub-types, 6 tagged with Inherited ichthyosis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inherited ichthyosis
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Netherton syndrome 15 trials
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Autosomal recessive congenital ichthyosis 2 trials · 10 incl. sub-types
13 sub-types
- Exfoliative ichthyosis 0 trials · 6 incl. sub-types Sub-types →
- Autosomal recessive congenital ichthyosis 1 2 trials
- Congenital non-bullous ichthyosiform erythroderma 0 trials · 1 incl. sub-types Sub-types →
- Acral self-healing collodion baby 0 trials
- Autosomal recessive congenital ichthyosis 11 0 trials
- Autosomal recessive congenital ichthyosis 4A 0 trials Sub-types →
- Autosomal recessive congenital ichthyosis 5 0 trials
- Autosomal recessive congenital ichthyosis 8 0 trials
- Bathing suit ichthyosis 0 trials
- Ichthyosis, congenital, autosomal recessive 12 0 trials
- Ichthyosis, congenital, autosomal recessive 13 0 trials
- Ichthyosis, congenital, autosomal recessive 14 0 trials
- Self-healing collodion baby 0 trials Sub-types →
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Keratinopathic ichthyosis 0 trials · 7 incl. sub-types
5 sub-types
- Superficial epidermolytic ichthyosis 6 trials
- Epidermolytic ichthyosis 1 trial Sub-types →
- Congenital reticular ichthyosiform erythroderma 0 trials
- Epidermolytic nevus 0 trials
- Ichthyosis hystrix of Curth-Macklin 0 trials
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Ichthyosis vulgaris 3 trials
1 sub-type
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Recessive X-linked ichthyosis 2 trials
1 sub-type
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Peeling skin syndrome 1 trial
5 sub-types
- Acral peeling skin syndrome 0 trials
- Generalized peeling skin syndrome 0 trials Sub-types →
- Peeling skin syndrome 4 0 trials
- Peeling skin syndrome 5 0 trials
- Peeling skin syndrome 6 0 trials
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IFAP syndrome 0 trials
2 sub-types
- IFAP syndrome 1, with or without BRESHECK syndrome 0 trials
- IFAP syndrome 2 0 trials
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Ichthyosis hystrix 0 trials
2 sub-types
- Ichthyosis histrix, Lambert type 0 trials
- Ichthyosis hystrix of Curth-Macklin 0 trials
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Ichthyosis linearis circumflexa 0 trials
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Ichthyosis with erythrokeratoderma 0 trials
Most studied deeper sub-types
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Experimental drug for rare skin disease fails to reach goal
Disease control Stopped earlyThis early-stage trial tested a drug called DS-2325a in 9 adults with Netherton syndrome, a rare genetic condition causing severe skin redness, scaling, and allergies. The study aimed to check safety and whether the drug could help control the disease. However, the trial was term…
Phase 1/2 • Sponsor: Daiichi Sankyo • Aim: Disease control
Last updated Jun 27, 2026 12:33 UTC
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Hope for rare skin disease: new drug shows promise in trial
Disease control Stopped earlyThis study tested a medicine called spesolimab for people with Netherton syndrome, a rare genetic skin condition causing severe redness and scaling. About 43 people aged 12 and older took part, receiving either the drug or a placebo. The goal was to see if spesolimab could reduce…
Phase 2/3 • Sponsor: Boehringer Ingelheim • Aim: Disease control
Last updated Jun 27, 2026 11:00 UTC
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Promising ichthyosis drug trial stalls after just 5 patients
Disease control Stopped earlyThis 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 2 • Sponsor: Vanda Pharmaceuticals • Aim: Disease control
Last updated Jun 26, 2026 17:50 UTC
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Rare skin disease study seeks to understand netherton syndrome
Knowledge-focused Stopped earlyThis study aimed to collect real-world data on Netherton Syndrome, a rare genetic skin disorder. Researchers planned to follow 4 participants over 52 weeks, measuring skin severity and other symptoms. The study was terminated early, so results are limited.
Sponsor: Boehringer Ingelheim • Aim: Knowledge-focused
Last updated Jun 27, 2026 14:03 UTC