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Type I interferonopathies are rare autoinflammatory disorders caused by genetic defects and associated with significant morbidity and mortality. These diseases are refractory to conventional immunosup...
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Lead Sponsor
Imagine Institute
NCT00001373 · Familial Mediterranean Fever (FMF), Autoinflammation, and more
NCT06672237 · Neuromuscular Disease, Neuromuscular Diseases (NMD), and more
NCT05645003 · Spinal Cord Injuries, Neuropathic Pain, and more
NCT07365254 · Genetic Disease
NCT04806620 · Post-Acute COVID-19 Syndrome, ME/CFS, and more
Medical University Innsbruck
Innsbruck
Antwerp University Hospital
Antwerp
Children's Hospital Zagreb
Zagreb
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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