Clin2
NCT06724562Possibly a fitRecruiting

Anti-IL1 therapy for severe FOP flare-ups

Fibrodysplasia Ossificans Progressiva (FOP)

Part of Bones, joints & muscles clinical trials.

This trial is for people with FOP who have severe, frequent flare-ups. It follows those who are already starting an anti-IL1 medication (like anakinra) to see if it helps reduce flares and improve symptoms.

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

Phase
N/A
Enrollment
11 people
Ages
6 years to 30 years
Study type
Observational

Who can take part

  • You have been diagnosed with classic FOP (the R206H gene change) and are between 6 and 30 years old.
  • You have frequent flare-ups—more than 4 per year—or a flare that has lasted over a month without getting better.
  • Your doctor has already decided to start you on an anti-IL1 medication (like anakinra or canakinumab).
  • You are able to travel to UCSF for study visits, blood draws, and scans.
  • You do not have a history of unexplained infections, autoimmune disease, or a reason you cannot take anti-IL1 therapy.

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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