Evaluation of the pharmacokinetic equivalence and 54-week efficacy and safety of CT-P13 and innovator infliximab in Japanese patients with rheumatoid arthritis.

scientific article published on 4 March 2015

Evaluation of the pharmacokinetic equivalence and 54-week efficacy and safety of CT-P13 and innovator infliximab in Japanese patients with rheumatoid arthritis. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.3109/14397595.2015.1022297
P932PMC publication ID4732515
P698PubMed publication ID25736355
P5875ResearchGate publication ID273151851

P50authorHisashi YamanakaQ88712489
Kazuyoshi SaitoQ98839521
Tsutomu TakeuchiQ40949081
P2093author name stringYoshiya Tanaka
Sang Joon Lee
Takeo Sakurai
Yoshihiro Nambu
Hideo Ohtsubo
P2860cites workAcute phase reactants add little to composite disease activity indices for rheumatoid arthritis: validation of a clinical activity scoreQ24817087
The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritisQ27860872
Infliximab (chimeric anti-tumour necrosis factor alpha monoclonal antibody) versus placebo in rheumatoid arthritis patients receiving concomitant methotrexate: a randomised phase III trial. ATTRACT Study GroupQ33885648
Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritisQ34315745
Efficacy and safety of ascending methotrexate dose in combination with adalimumab: the randomised CONCERTO trialQ35605449
Physicochemical characterization of RemsimaQ36213623
A randomised, double-blind, parallel-group study to demonstrate equivalence in efficacy and safety of CT-P13 compared with innovator infliximab when coadministered with methotrexate in patients with active rheumatoid arthritis: the PLANETRA studyQ37206622
A randomised, double-blind, multicentre, parallel-group, prospective study comparing the pharmacokinetics, safety, and efficacy of CT-P13 and innovator infliximab in patients with ankylosing spondylitis: the PLANETAS studyQ37206628
Impact of trough serum level on radiographic and clinical response to infliximab plus methotrexate in patients with rheumatoid arthritis: results from the RISING studyQ37380288
Development and validation of response criteria in rheumatoid arthritis: steps towards an international consensus on prognostic markersQ41930269
A simplified disease activity index for rheumatoid arthritis for use in clinical practiceQ44321551
Drug levels, anti-drug antibodies, and clinical efficacy of the anti-TNFα biologics in rheumatic diseasesQ44616013
American College of Rheumatology. Preliminary definition of improvement in rheumatoid arthritisQ47643186
Measurement of patient outcome in arthritisQ56879288
The relationship of serum infliximab concentrations to clinical improvement in rheumatoid arthritis: results from ATTRACT, a multicenter, randomized, double-blind, placebo-controlled trialQ74455184
Should improvement in rheumatoid arthritis clinical trials be defined as fifty percent or seventy percent improvement in core set measures, rather than twenty percent?Q77341371
P433issue6
P921main subjectrheumatoid arthritisQ187255
pharmacokineticsQ323936
P304page(s)817-824
P577publication date2015-04-02
P1433published inModern RheumatologyQ15752709
P1476titleEvaluation of the pharmacokinetic equivalence and 54-week efficacy and safety of CT-P13 and innovator infliximab in Japanese patients with rheumatoid arthritis
P478volume25

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cites work (P2860)
Q36303459A practical guide about biosimilar data for health care providers treating inflammatory diseases
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Q26746634Biosimilars in Inflammatory Bowel Disease: Facts and Fears of Extrapolation
Q47688424Biosimilars in rheumatology: A review of the evidence and their place in the treatment algorithm
Q90083372Biosimilars versus biologics for inflammatory conditions
Q38676104CT-P13 in the treatment of rheumatoid arthritis.
Q47418286Comparative effectiveness of the biosimilar CT-P13.
Q28066776Experience with biosimilar infliximab (CT-P13) in paediatric patients with inflammatory bowel diseases
Q88698802Global Acceptance of Biosimilars: Importance of Regulatory Consistency, Education, and Trust
Q39371316Immunogenicity of Biologics in Chronic Inflammatory Diseases: A Systematic Review
Q38960108Infliximab Biosimilar (CT-P13; Infliximab-dyyb): A Review in Autoimmune Inflammatory Diseases
Q92680304Infliximab biosimilar CT-P13 is interchangeable with its originator for patients with inflammatory bowel disease in real world practice
Q58798380Non-medical Switching from Originator Tumor Necrosis Factor Inhibitors to Their Biosimilars: Systematic Review of Randomized Controlled Trials and Real-World Studies
Q57174419Practical Guidance on Biosimilars, With a Focus on Latin America: What Do Rheumatologists Need to Know?
Q39430200Safety and efficacy of CT-P13 in Japanese patients with rheumatoid arthritis in an extension phase or after switching from infliximab.
Q33840949Switching Between Reference Biologics and Biosimilars for the Treatment of Rheumatology, Gastroenterology, and Dermatology Inflammatory Conditions: Considerations for the Clinician
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