Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Autosomal recessive congenital ichthyosis 8

MONDO:0013495

Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the LIPN gene.

Also known as: ARCI8, autosomal recessive congenital ichthyosis type 8, ichthyosis, congenital, autosomal recessive type 8, ichthyosis, congenital, autosomal recessive 8, ichthyosis, lamellar, 4, ichthyosis, lamellar, 4, formerly, lamellar ichthyosis, late-onset

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

Follow this condition — get notified about new trials

Broader categories

Disease (680) Hereditary disease (176) Skin disorder (132) Eye disorder (102) Human disease (14) Ichthyosis (12) Hereditary skin disorder (6) Inherited ichthyosis (6) Lamellar ichthyosis (4) Disorder of orbital region (3)
Not yet finished but already full! 1 Completed 1 Terminated 1
Sort by
  • 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

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space