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Mavrilimumab, a Fully Human Granulocyte-Macrophage Colony-Stimulating Factor Receptor alpha Monoclonal Antibody Long-Term Safety and Efficacy in Patients With Rheumatoid Arthritis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023728%3A_____%2F18%3AN0000050" target="_blank" >RIV/00023728:_____/18:N0000050 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/art.40420|" target="_blank" >https://doi.org/10.1002/art.40420|</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/art.40420" target="_blank" >10.1002/art.40420</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Mavrilimumab, a Fully Human Granulocyte-Macrophage Colony-Stimulating Factor Receptor alpha Monoclonal Antibody Long-Term Safety and Efficacy in Patients With Rheumatoid Arthritis

  • Original language description

    Mavrilimumab, a human monoclonal antibody, targets granulocyte-macrophage colony-stimulating factor receptor . We undertook to determine the long-term safety and efficacy of mavrilimumab in rheumatoid arthritis patients in 2 phase IIb studies (1071 and 1107) and in 1 open-label extension study (ClinicalTrials.gov identifier: NCT01712399. In study 1071, patients with an inadequate response to disease-modifying antirheumatic drugs (DMARDs) received mavrilimumab (30, 100, or 150 mg) or placebo every other week plus methotrexate. In study 1107, patients with an inadequate response to anti-tumor necrosis factor agents and/or DMARDs received 100 mg mavrilimumab every other week or 50 mg golimumab every 4 weeks plus methotrexate. Patients entering the open-label extension study received 100 mg mavrilimumab every other week plus methotrexate. Long-term safety and efficacy of mavrilimumab were assessed

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30226 - Rheumatology

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    ARTHRITIS & RHEUMATOLOGY

  • ISSN

    2326-5191

  • e-ISSN

    2326-5205

  • Volume of the periodical

    70

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    679-689

  • UT code for WoS article

    000430912600007

  • EID of the result in the Scopus database

    2-s2.0-85044627852