Efficacy, safety and immunogenicity of GP2015, an etanercept biosimilar, compared with the reference etanercept in patients with moderate-to-severe rheumatoid arthritis: 24-week results from the comparative phase III, randomised, double-blind EQUIRA

scholarly article by Marco Matucci-Cerinic et al published 2018 in RMD open

Efficacy, safety and immunogenicity of GP2015, an etanercept biosimilar, compared with the reference etanercept in patients with moderate-to-severe rheumatoid arthritis: 24-week results from the comparative phase III, randomised, double-blind EQUIRA is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1136/RMDOPEN-2018-000757
P932PMC publication ID6242015
P698PubMed publication ID30487998

P50authorMarco Matucci-CerinicQ19859583
Maya Hema BuchQ44940582
Eugene Joseph KucharzQ66419555
P2093author name stringYannick Allanore
Hendrik Schulze-Koops
Arthur Kavanaugh
Arnd Schwebig
Johann Poetzl
Heike Woehling
Goran Babic
Adanna Davis
P2860cites workACR/EULAR 2010 rheumatoid arthritis classification criteriaQ26864171
A trial of etanercept, a recombinant tumor necrosis factor receptor:Fc fusion protein, in patients with rheumatoid arthritis receiving methotrexateQ28295474
Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritisQ34315745
The Functional Assessment of Cancer Therapy scale: development and validation of the general measureQ34361336
Development and validation of the European League Against Rheumatism response criteria for rheumatoid arthritis. Comparison with the preliminary American College of Rheumatology and the World Health Organization/International League Against RheumatiQ34662758
Etanercept: An overviewQ35190102
Etanercept and sulfasalazine, alone and combined, in patients with active rheumatoid arthritis despite receiving sulfasalazine: a double-blind comparisonQ35637985
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Recommendations for the validation of immunoassays used for detection of host antibodies against biotechnology productsQ37321197
A phase III randomised, double-blind, parallel-group study comparing SB4 with etanercept reference product in patients with active rheumatoid arthritis despite methotrexate therapyQ37604518
GP2015, a proposed etanercept biosimilar: Pharmacokinetic similarity to its reference product and comparison of its autoinjector device with prefilled syringesQ37695053
Longterm safety, efficacy, and radiographic outcome with etanercept treatment in patients with early rheumatoid arthritisQ44003346
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State-of-the-art immunogenicity evaluation in phase 3 confirmatory study (EGALITY) with etanercept biosimilar GP2015.Q50098933
Once-weekly administration of 50 mg etanercept in patients with active rheumatoid arthritis: results of a multicenter, randomized, double-blind, placebo-controlled trial.Q51051064
The EGALITY study: a confirmatory, randomized, double-blind study comparing the efficacy, safety and immunogenicity of GP2015, a proposed etanercept biosimilar, vs. the originator product in patients with moderate-to-severe chronic plaque-type psoriQ51359715
A phase III, multicentre, randomised, double-blind, active-controlled, parallel-group trial comparing safety and efficacy of HD203, with innovator etanercept, in combination with methotrexate, in patients with rheumatoid arthritis: the HERA study.Q53170870
Phase III, multicentre, double-blind, randomised, parallel-group study to evaluate the similarities between LBEC0101 and etanercept reference product in terms of efficacy and safety in patients with active rheumatoid arthritis inadequately respondinQ54967818
Measurement of patient outcome in arthritisQ56879288
Validation of the 28-joint Disease Activity Score (DAS28) and European League Against Rheumatism response criteria based on C-reactive protein against disease progression in patients with rheumatoid arthritis, and comparison with the DAS28 based on eQ63101754
The American College of Rheumatology 1991 revised criteria for the classification of global functional status in rheumatoid arthritisQ68109843
Measuring fatigue and other anemia-related symptoms with the Functional Assessment of Cancer Therapy (FACT) measurement systemQ73206828
A comparison of etanercept and methotrexate in patients with early rheumatoid arthritisQ73235899
Etanercept versus methotrexate in patients with early rheumatoid arthritis: two-year radiographic and clinical outcomesQ74455180
Biosimilars-why terminology mattersQ84709013
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectrheumatoid arthritisQ187255
P304page(s)e000757
P577publication date2018-01-01
P1433published inRMD openQ27726913
P1476titleEfficacy, safety and immunogenicity of GP2015, an etanercept biosimilar, compared with the reference etanercept in patients with moderate-to-severe rheumatoid arthritis: 24-week results from the comparative phase III, randomised, double-blind EQUIRA
P478volume4

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cites work (P2860)
Q91944393A Comparative Study to Assess the Efficacy, Safety, and Immunogenicity of YLB113 and the Etanercept Reference Product for the Treatment of Patients with Rheumatoid Arthritis
Q90083372Biosimilars versus biologics for inflammatory conditions
Q89600836Efficacy of pharmacological treatment in rheumatoid arthritis: a systematic literature research informing the 2019 update of the EULAR recommendations for management of rheumatoid arthritis
Q92771591Pooled analysis of TNF inhibitor biosimilar studies comparing radiographic progression by disease activity states in rheumatoid arthritis
Q64922356Switch from reference etanercept to SDZ ETN, an etanercept biosimilar, does not impact efficacy, safety, and immunogenicity of etanercept in patients with moderate-to-severe rheumatoid arthritis: 48-week results from the phase III, randomized, doubl

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