Therapeutic Arthritis Research & Gastrointestinal Event Trial (TARGET)
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Introduction
Study characteristics:
18,325 patients > 50 years of age with osteoarthritis
Patients ramdomized to treatment group for 52 weeks:
Results:
- among patients who did not take 81 mg aspirin,the lumiracoxib group had significantly fewer peptic ulcer complications
- no signficant difference in peptic ulcer complications was found in patients taking 81 mg of aspirin
- elevated serum transaminases noted in the lumiracoxib group
More general terms
Additional terms
References
- ↑ Schnitzer TJ, Burmester GR, Mysler E, Hochberg MC, Doherty M, Ehrsam E, Gitton X, Krammer G, Mellein B, Matchaba P, Gimona A, Hawkey CJ; TARGET Study Group. Comparison of lumiracoxib with naproxen and ibuprofen in the Therapeutic Arthritis Research and Gastrointestinal Event Trial (TARGET), reduction in ulcer complications: randomised controlled trial. Lancet. 2004 Aug 21;364(9435):665-74. PMID: https://www.ncbi.nlm.nih.gov/pubmed/15325831
- ↑ Farkouh ME, Kirshner H, Harrington RA, Ruland S, Verheugt FW, Schnitzer TJ, Burmester GR, Mysler E, Hochberg MC, Doherty M, Ehrsam E, Gitton X, Krammer G, Mellein B, Gimona A, Matchaba P, Hawkey CJ, Chesebro JH; TARGET Study Group. Comparison of lumiracoxib with naproxen and ibuprofen in the Therapeutic Arthritis Research and Gastrointestinal Event Trial (TARGET), cardiovascular outcomes: randomised controlled trial. Lancet. 2004 Aug 21;364(9435):675-84. PMID: https://www.ncbi.nlm.nih.gov/pubmed/15325832
- ↑ Journal Watch 24(19):149, 2004