DEODHAR, A., R. BLANCO, Eva DOKOUPILOVÁ, M. VAN DE SANDE, S. HALL, A. WIKSTEN, B. O. PORTER, H. O. RICHARDS, S. HAEMMERLE and J. BRAUNS. SECUKINUMAB SIGNIFICANTLY IMPROVED SIGNS AND SYMPTOMS OF NON-RADIOGRAPHIC AXIAL SPONDYLOARTHIUTIS: 16-WEEK RESULTS FROM THE PHASE-III PREVENT STUDY. 2020.
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Basic information
Original name SECUKINUMAB SIGNIFICANTLY IMPROVED SIGNS AND SYMPTOMS OF NON-RADIOGRAPHIC AXIAL SPONDYLOARTHIUTIS: 16-WEEK RESULTS FROM THE PHASE-III PREVENT STUDY
Authors DEODHAR, A., R. BLANCO, Eva DOKOUPILOVÁ (203 Czech Republic, belonging to the institution), M. VAN DE SANDE, S. HALL, A. WIKSTEN, B. O. PORTER, H. O. RICHARDS, S. HAEMMERLE and J. BRAUNS.
Edition 2020.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 30104 Pharmacology and pharmacy
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
RIV identification code RIV/00216224:14160/20:00118265
Organization unit Faculty of Pharmacy
UT WoS 000530661500218
Keywords in English secukinumab; signs; symptoms; non radiographic axial; spondyloarthritis; prevent study
Tags rivok, ÚFT
Tags International impact, Reviewed
Changed by Changed by: JUDr. Sabina Krejčiříková, učo 383857. Changed: 30/8/2022 14:43.
Abstract
Our findings indicate that secukinumab 150 mg provides significant and sustained improvement in signs and symptoms of nonradiographic axial SpA through 52 weeks. Safety was consistent with previous reports
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