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Tralokinumab for moderate-to-severe UC: a randomised, double-blind, placebo-controlled, phase IIa study

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F15%3A10292682" target="_blank" >RIV/00216208:11110/15:10292682 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1136/gutjnl-2014-308004" target="_blank" >http://dx.doi.org/10.1136/gutjnl-2014-308004</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1136/gutjnl-2014-308004" target="_blank" >10.1136/gutjnl-2014-308004</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Tralokinumab for moderate-to-severe UC: a randomised, double-blind, placebo-controlled, phase IIa study

  • Original language description

    Objective Interleukin-13 (IL-13) has been implicated as a key driver of UC. This trial evaluates the efficacy and safety of tralokinumab, an IL-13-neutralising antibody, as add-on therapy in adults with moderate-to-severe UC despite standard treatments.Design Non-hospitalised adults with UC (total Mayo score >= 6) were randomised to receive tralokinumab 300 mg or placebo subcutaneously every 2 weeks for 12 weeks. The primary end point was the rate of clinical response at week 8. Secondary efficacy endpoints included clinical remission and mucosal healing rates at week 8 and changes in total Mayo score, total modified Riley score, partial Mayo score and disease activity markers. Results Clinical response rate was 38% (21/56) for tralokinumab vs 33% (18/55) for placebo (p=0.406). Clinical remission rate was 18% (10/56) vs 6% (3/55) (p=0.033) and mucosal healing rate was 32% (18/56) vs 20% (11/55) (p=0.104) for tralokinumab vs placebo. Changes to week 8 in total Mayo score and total mod

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FE - Other fields of internal medicine

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Gut

  • ISSN

    0017-5749

  • e-ISSN

  • Volume of the periodical

    64

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

    243-249

  • UT code for WoS article

    000348449800011

  • EID of the result in the Scopus database

    2-s2.0-84920942417