dc.contributor.author
Balazcs, Eva
dc.contributor.author
Sieper, Joachim
dc.contributor.author
Bickham, Kara
dc.contributor.author
Mehta, Anish
dc.contributor.author
Frontera, Nancy
dc.contributor.author
Stryszak, Paul
dc.contributor.author
Popmihajlov, Zoran
dc.contributor.author
Peloso, Paul M.
dc.date.accessioned
2018-06-08T10:20:11Z
dc.date.available
2017-04-25T12:00:22.661Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/20263
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-23567
dc.description.abstract
Background This study evaluated two doses of etoricoxib (60 and 90 mg) vs.
naproxen 1000 mg in subjects with ankylosing spondylitis (AS). Methods This
was a 2-part, double-blind, active comparator-controlled non-inferiority study
in subjects ≥18 years of age with AS. In Part I, subjects were randomized to
naproxen 1000 mg; etoricoxib 60 mg, and 90 mg. In Part II, naproxen and
etoricoxib 90 mg subjects continued on the same treatment; subjects on
etoricoxib 60 mg either continued on 60 mg or escalated to 90 mg. Part I (6
weeks) assessed the efficacy of A) etoricoxib 60 mg vs. naproxen and B) 90 mg
vs. naproxen according to the time-weighted average change from baseline in
Spinal Pain Intensity (SPI; 0–100 mm VAS) (primary endpoint). The non-
inferiority margin was set at 8 mm for SPI. In Part II (20 weeks) we evaluated
the potential benefit of increasing from 60 to 90 mg (predefined minimum
clinically important difference = 6 mm in SPI) for inadequate responders (<50
% improvement from baseline in SPI) onetoricoxib 60 mg in Part I. Results In
total, 1015 subjects were randomized to receive etoricoxib 60 mg (N = 702),
etoricoxib 90 mg (N = 156), and naproxen 1000 mg (N = 157); 70.9 % were male
and the mean age was 45.2 years. There were 919 subjects who completed Part I
and all continued to Part II. In Part I, SPI change was non-inferior for both
etoricoxib doses vs. naproxen. In both Part I and II, the incidence of adverse
events (AEs), drug-related AEs, and serious adverse events (SAEs) were similar
between the 3 treatment groups. Conclusion Both doses of etoricoxib were non-
inferior to naproxen. All treatments were well tolerated. Etoricoxib 60 and 90
mg effectively control pain in patients with AS, with 60 mg once daily as the
lowest effective dose for most patients. Trial registration Clinical Trials
Registry # NCT01208207. Registered on 22 September 2010.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Ankylosing spondylitis
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
A randomized, clinical trial to assess the relative efficacy and tolerability
of two doses of etoricoxib versus naproxen in patients with ankylosing
spondylitis
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
BMC Musculoskeletal Disorders. - 17 (2016), Artikel Nr. 426
dcterms.bibliographicCitation.doi
10.1186/s12891-016-1275-5
dcterms.bibliographicCitation.url
http://bmcmusculoskeletdisord.biomedcentral.com/articles/10.1186/s12891-016-1275-5
refubium.affiliation
Charité - Universitätsmedizin Berlin
de
refubium.mycore.fudocsId
FUDOCS_document_000000026881
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000008098
dcterms.accessRights.openaire
open access