| Literature DB >> 26503347 |
Roy Altman1, Marc Hochberg2, Allan Gibofsky3, Mark Jaros4, Clarence Young5.
Abstract
OBJECTIVE: Nonsteroidal anti-inflammatory drugs (NSAIDs) such as meloxicam are commonly used to treat osteoarthritis (OA) but are associated with potentially serious dose-related adverse events (AEs). SoluMatrix meloxicam has been developed with the goal of enabling effective treatment at low doses. This phase 3 study evaluated the efficacy and safety of low-dose SoluMatrix meloxicam capsules 5 mg and 10 mg administered once daily for 12 weeks in patients with OA-related pain. RESEARCH DESIGN AND METHODS: This randomized, double-blind study enrolled patients ≥40 years of age with confirmed hip or knee OA (Kellgren-Lawrence grade II-III) who were chronic users of NSAIDs and/or acetaminophen for OA pain and had Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain subscale mean scores ≥40 mm. Eligible patients experienced an OA pain flare (defined as a ≥15 mm increase in the WOMAC pain subscale score) following discontinuation of NSAIDs/acetaminophen. Patients were randomized to receive once-daily SoluMatrix meloxicam 5 mg or 10 mg, or placebo for 12 weeks. ClinicalTrials.gov identifier: NCT01787188. MAIN OUTCOME MEASURES: The primary outcome measure was the mean change from baseline in WOMAC pain subscale score at week 12.Entities:
Keywords: Chronic pain; Low-dose SoluMatrix meloxicam; NSAIDs; Osteoarthritis
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Year: 2015 PMID: 26503347 DOI: 10.1185/03007995.2015.1112772
Source DB: PubMed Journal: Curr Med Res Opin ISSN: 0300-7995 Impact factor: 2.580