epidermolytic ichthyosis

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Epidermal Growth Factor Receptor Inhibition for Keratinopathies	Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Ichthyosiform Erythroderma, Congenital, Infant, Newborn, Diseases, Keratoderma, Palmoplantar, Skin Abnormalities, Skin and Connective Tissue Diseases, ectodermal dysplasia syndrome, epidermolytic ichthyosis, hereditary disease, hereditary skin disorder, ichthyosis, keratosis, nail disorder, pachyonychia congenita, skin disorder	Not yet recruiting	Phase 1 / Phase 2	2026-08-03		NCT06545695

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