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These clinical study results are supplied for informational purposes only in the interests of scientific disclosure. They are not intended to substitute for the FDA-approved package insert or other approved labeling.

Drug Details

Company Name Business Partner Drug Name Generic Name Unique ID Studied Indications or Disease Phase Approved Drug Label
Pfizer Inc. Bextra valdecoxib NCT00650455 Rheumatoid Arthritis Phase IV Bextra is no longer marketed in the United States
Clinical Study Summary Protocol No. A3471018: Multicenter, double-blind, randomized, placebo controlled, comparison of the efficacy and safety of Bextra® (valdecoxib) 10 mg once daily and naproxen 500 mg twice daily in treating the signs and symptoms of rheumatoid arthritis (RA) in a severe RA population.

Link to ClinicalTrials.gov Registration:
http://www.clinicaltrials.gov/ct2/show/NCT00650455?term=a3471018&rank=1


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Company Study
Protocol No. A3471018
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