Journal article
Impact of concomitant low-dose aspirin on the safety and tolerability of naproxen and esomeprazole magnesium delayed-release tablets in patients requiring chronic nonsteroidal anti-inflammatory drug therapy: An analysis from 5 Phase III studies
DJ Angiolillo, C Datto, S Raines, ND Yeomans
Journal of Thrombosis and Thrombolysis | SPRINGER | Published : 2014
Abstract
Patients receiving chronic nonsteroidal anti-inflammatory drugs (NSAIDs) and concomitant low-dose aspirin (LDA) are at increased risk of gastrointestinal (GI) toxicity. A fixed-dose combination of enteric-coated (EC) naproxen and immediate-release esomeprazole magnesium (NAP/ESO) has been designed to deliver a proton-pump inhibitor followed by an NSAID in a single tablet. To examine safety data from 5 Phase III studies of NAP/ESO in LDA users (≤325 mg daily, administered at any time during the study), and LDA non-users, data were analyzed from 6-month studies assessing NAP/ESO versus EC naproxen in patients with osteoarthritis, rheumatoid arthritis, or ankylosing spondylitis (n = 2), 3-month..
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Funding Acknowledgements
These studies were sponsored and conducted by POZEN Inc. Lisa Suchower of AstraZeneca provided assistance in the statistical analysis of the data. Medical writing support was provided by Rhian Harper Owen, on behalf of Complete Medical Communications, funded by AstraZeneca.