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A randomized, double-blind, placebo-controlled 12-week trial of infliximab in patients with juvenile-onset spondyloarthritis
by
Ramiro, Sofia
, van der Heijde, Desirée
, Burgos-Vargas, Rubén
, Reding-Bernal, Arturo
, Vázquez-Mellado, Janitzia
, Alvarez-Hernandez, Everardo
, Loyola-Sanchez, Adalberto
in
Active joint counts
/ Antibiotics
/ Arthritis
/ Children
/ Clinical medicine
/ Clinical trials
/ Demographic aspects
/ Development and progression
/ Dosage and administration
/ Double-blind studies
/ Evaluation
/ Guardians
/ Health aspects
/ Infliximab
/ Juvenile arthritis
/ Juvenile SpA
/ Medicine
/ Medicine & Public Health
/ Methods
/ Monoclonal antibodies
/ Nonsteroidal anti-inflammatory drugs
/ Open-label study
/ Orthopedics
/ Pain
/ Patients
/ Pediatrics
/ Placebos
/ Randomized trial
/ Range of motion
/ Remission (Medicine)
/ Rheumatology
/ Sacroiliitis
/ Spondyloarthritis
/ Spondyloarthropathies
/ Teenagers
/ TNF inhibitors
/ Tuberculosis
/ Tumor necrosis factor-TNF
2022
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A randomized, double-blind, placebo-controlled 12-week trial of infliximab in patients with juvenile-onset spondyloarthritis
by
Ramiro, Sofia
, van der Heijde, Desirée
, Burgos-Vargas, Rubén
, Reding-Bernal, Arturo
, Vázquez-Mellado, Janitzia
, Alvarez-Hernandez, Everardo
, Loyola-Sanchez, Adalberto
in
Active joint counts
/ Antibiotics
/ Arthritis
/ Children
/ Clinical medicine
/ Clinical trials
/ Demographic aspects
/ Development and progression
/ Dosage and administration
/ Double-blind studies
/ Evaluation
/ Guardians
/ Health aspects
/ Infliximab
/ Juvenile arthritis
/ Juvenile SpA
/ Medicine
/ Medicine & Public Health
/ Methods
/ Monoclonal antibodies
/ Nonsteroidal anti-inflammatory drugs
/ Open-label study
/ Orthopedics
/ Pain
/ Patients
/ Pediatrics
/ Placebos
/ Randomized trial
/ Range of motion
/ Remission (Medicine)
/ Rheumatology
/ Sacroiliitis
/ Spondyloarthritis
/ Spondyloarthropathies
/ Teenagers
/ TNF inhibitors
/ Tuberculosis
/ Tumor necrosis factor-TNF
2022
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A randomized, double-blind, placebo-controlled 12-week trial of infliximab in patients with juvenile-onset spondyloarthritis
by
Ramiro, Sofia
, van der Heijde, Desirée
, Burgos-Vargas, Rubén
, Reding-Bernal, Arturo
, Vázquez-Mellado, Janitzia
, Alvarez-Hernandez, Everardo
, Loyola-Sanchez, Adalberto
in
Active joint counts
/ Antibiotics
/ Arthritis
/ Children
/ Clinical medicine
/ Clinical trials
/ Demographic aspects
/ Development and progression
/ Dosage and administration
/ Double-blind studies
/ Evaluation
/ Guardians
/ Health aspects
/ Infliximab
/ Juvenile arthritis
/ Juvenile SpA
/ Medicine
/ Medicine & Public Health
/ Methods
/ Monoclonal antibodies
/ Nonsteroidal anti-inflammatory drugs
/ Open-label study
/ Orthopedics
/ Pain
/ Patients
/ Pediatrics
/ Placebos
/ Randomized trial
/ Range of motion
/ Remission (Medicine)
/ Rheumatology
/ Sacroiliitis
/ Spondyloarthritis
/ Spondyloarthropathies
/ Teenagers
/ TNF inhibitors
/ Tuberculosis
/ Tumor necrosis factor-TNF
2022
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A randomized, double-blind, placebo-controlled 12-week trial of infliximab in patients with juvenile-onset spondyloarthritis
Journal Article
A randomized, double-blind, placebo-controlled 12-week trial of infliximab in patients with juvenile-onset spondyloarthritis
2022
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Overview
Objective
To assess the efficacy and safety of infliximab versus placebo in the treatment of patients with juvenile-onset spondyloarthritis (JoSpA).
Methods
Phase III, randomized, double-blind, placebo-controlled trial of 12 weeks that included patients ≤ 18 years old with JoSpA not responding to nonsteroidal anti-inflammatory drugs, sulfasalazine, or methotrexate. Patients were randomly assigned 1:1 to the infusion of infliximab 5mg/kg or placebo; completers entered then an open-label extension (OLE) period of 42 weeks. The primary endpoint was the number of active joints. Secondary outcomes included the assessment of disease activity, tender entheses, spinal mobility, serum C-reactive protein (CRP), the Bath Ankylosing Spondylitis Disease Activity and Functional Index, and the Childhood Health Assessment Questionnaire (CHAQ).
Results
We randomized 12 patients to infliximab and 14 to placebo. No significant differences were found between groups at baseline. At week 12, the mean number of active joints was 1.4 (SD 2.4) in the infliximab group and 4.1 (SD 3.0) in the placebo group (
p
= 0.0002). A repeated-measures mixed model analysis that included all endpoints in the study demonstrated sustained favourable outcomes of infliximab for active joints, tender joints, swollen joints, and tender enthesis counts, as well as for CHAQ and CRP (
p
< 0.01). Adverse events were more frequent in the infliximab group, including infections and infusion reactions, but none of them was serious.
Conclusion
Infliximab is efficacious for patients with JoSpA with an inadequate response to conventional treatment. No serious adverse events with the use of infliximab were observed.
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