Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Familial idiopathic inflammatory myopathy

MONDO:0600024

An instance of myositis that is caused by an inherited genomic modification in an individual, and has an unknown cause.

Also known as: familial idiopathic myositis

8 clinical trials for this condition and its sub-types, 0 tagged with Familial idiopathic inflammatory myopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Idiopathic inflammatory myopathy (181)
Including sub-types (8) Tagged with Familial idiopathic inflammatory myopathy (0)
Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1
Sort by
  • Can a new pill ease muscle weakness in myositis?

    Disease control Not yet recruiting

    This phase III trial tests whether the oral drug nerandomilast can improve symptoms of idiopathic inflammatory myopathies, a group of rare autoimmune diseases that cause muscle weakness and inflammation. Adults with active myositis are randomly assigned to take nerandomilast or a…

    Phase 3 • Sponsor: Boehringer Ingelheim • Aim: Disease control

    Last updated Sep 18, 2026 00:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse Glossary About Terms of use Contact us

This is a site from Cyber and Space