Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Hoffmann-La Roche
Age
1–17
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Diagnosis of sJIA according to the International League of Associations for Rheumatology (ILAR) classification
History of inadequate clinical response (in the opinion of the treating physician) to Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) and corticosteroids
If a participant has received previous treatment with any biologic agents other than tocilizumab, these must have been discontinued according to the timelines defined by protocol prior to the baseline visit
Participants currently receiving tocilizumab by the intravenous (IV) route of administration and with well-controlled disease do not require a period of discontinuation of IV tocilizumab and should have their first dose of SC tocilizumab administered on the date that their next IV tocilizumab infusion would be due
Concurrent treatment with Disease Modifying Anti-Rheumatic Drugs (DMARDs) including methotrexate (MTX), NSAIDs, and oral corticosteroids are permitted at the discretion of the investigator
Participants of reproductive potential must be willing to use highly effective contraceptive methods
You may not be if
Prior discontinuation of IV tocilizumab because of inadequate clinical response or safety events (including hypersensitivity)
Participants with poorly controlled disease (in the opinion of the treating physician) despite current treatment with IV tocilizumab
sJIA that is well controlled by any treatment agent other than tocilizumab (Juvenile Arthritis Disease Activity Score of 71 Joints \[JADAS-71\] less than or equal to \[\<=\] 3.8 with no fever)
Participants who are wheelchair-bound or bedridden
Any other auto-immune, rheumatic disease, or overlapping syndrome other than sJIA
Lack of recovery from recent surgery or an interval of \<6 weeks since surgery at the time of the screening visit
Females who are pregnant, lactating, or intending to become pregnant during study conduct
Any significant concurrent medical or surgical condition that would jeopardize the participant's safety or ability to complete the study
Known Human Immunodeficiency Virus (HIV) infection or other acquired forms of immune compromise or inborn conditions characterized by a compromised immune system
History of alcohol, drug, or chemical abuse within 6 months of screening
Any active acute, subacute, chronic, or recurrent bacterial, viral, or systemic fungal infection or any major episode of infection requiring hospitalization or treatment during screening or treatment with IV antibiotics completed within 4 weeks of the screening visit or oral antibiotics completed within 2 weeks of the screening visit
History of atypical tuberculosis (TB) or active TB requiring treatment within 2 years prior to screening visit
Positive TB test at screening unless treated with anti-TB therapy for at least 4 weeks prior to receiving study drug
History of reactivation or new onset of a systemic infection such as herpes zoster or Epstein-Barr virus within 2 months of the screening visit
Hepatitis B surface antigen or hepatitis C antibody positivity or chronic viral or autoimmune hepatitis
History of concurrent serious gastrointestinal disorders such as ulcer or inflammatory bowel disease, Crohn's disease, ulcerative colitis, or other symptomatic lower gastrointestinal conditions
History of or current cancer or lymphoma
Uncontrolled diabetes mellitus with elevated glycosylated hemoglobin
Macrophage activation syndrome (MAS) within 3 months of the screening visit
