INCLUSION BODY MYOSITIS
Clinical trials for INCLUSION BODY MYOSITIS explained in plain language.
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Drug used in transplants could slow rare Muscle-Wasting disease
Disease control OngoingThis study is testing whether sirolimus, a medication used in organ transplants, can slow down or stop the progression of inclusion body myositis (IBM), a rare muscle-wasting disease. It will involve 140 adults with IBM who will take the drug or a placebo for 84 weeks to see if i…
Matched conditions: INCLUSION BODY MYOSITIS
Phase: PHASE3 • Sponsor: University of Kansas Medical Center • Aim: Disease control
Last updated Mar 16, 2026 15:26 UTC
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New test aims to stop dangerous falls for people with Muscle-Weakening diseases
Diagnosis ENROLLING_BY_INVITATIONThis study aims to create and validate a simple set of physical tests to better predict the risk of falling for people with various nerve and muscle disorders. Researchers will test 108 patients with conditions like muscular dystrophy and ALS using tasks like standing up from a c…
Matched conditions: INCLUSION BODY MYOSITIS
Sponsor: LMU Klinikum • Aim: Diagnosis
Last updated Mar 20, 2026 14:47 UTC
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Scientists track rare muscle disease over two years
Knowledge-focused OngoingThis study aims to better understand how a rare muscle-wasting disease called sporadic inclusion body myositis (sIBM) progresses over time. Researchers will observe 150 adults with sIBM for two years, tracking their physical function, strength, and breathing. The goal is to learn…
Matched conditions: INCLUSION BODY MYOSITIS
Sponsor: University of California, Irvine • Aim: Knowledge-focused
Last updated Apr 03, 2026 14:41 UTC