Clin2
NCT06545695Possibly a fitNot yet recruiting

Testing a pill for skin conditions caused by keratin gene changes

Epidermolytic IchthyosisPalmoplantar KeratodermaPachyonychia Congenita

Treatments studied

Part of Genetic & congenital, Skin clinical trials.

This study tests an oral medication called erlotinib (an EGFR inhibitor) to see if it can reduce the skin symptoms of keratinopathies like epidermolytic ichthyosis, epidermolytic palmoplantar keratoderma, and pachyonychia congenita. The goal is to improve skin condition and quality of life.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1/Phase 2
Enrollment
44 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be at least 18 years old.
  • You must have a confirmed genetic diagnosis of a keratinopathy, such as epidermolytic ichthyosis, epidermolytic palmoplantar keratoderma, or pachyonychia congenita.
  • Your skin symptoms must be moderate or severe in the areas being studied.
  • You must be able to stop taking certain medications (like oral retinoids, steroids, or topical treatments) for a period before and during the study.
  • You must be willing to have blood draws and skin biopsies for research.
  • You cannot have active infections on the study skin areas, recent major surgery, or a history of invasive cancer in the past 5 years.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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