Clin2
NCT07477769Worth exploringNot yet recruiting

Blood cell study for inherited ichthyosis with NIPAL4 gene mutation

Sezary SyndromeIchthyosis, Lamellar

Treatments studied

Part of Blood & lymphatic, Cancer, Genetic & congenital, Immune system & allergy, Skin clinical trials.

This study looks at blood cells in people with a rare form of ichthyosis caused by NIPAL4 gene mutations. It aims to understand how the immune system might be affected, which could help improve future care.

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

Phase
N/A
Enrollment
10 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must be 18 years old or older.
  • You must have a type of ichthyosis caused by a change in the NIPAL4 gene (confirmed by genetic testing).
  • You cannot have other inflammatory, infectious, or blood disorders.
  • You cannot be under legal guardianship, curatorship, or other protective measures.
  • You must be willing to participate and not object to the research.

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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