lumiracoxib
Device400 mg once daily, oral over 6 weeks
Other names: Prexige
NCT Number: NCT00637949
This safety study evaluated the incidence of gastrointestinal adverse events and edema in patients with osteoarthritis treated with lumiracoxib and rofecoxib as comparator
Looking for future studies?
Notify Me50 year–90 year
All sexes
Interventional
Phase 3
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other in and exclusion criteria may apply
400 mg once daily, oral over 6 weeks
Other names: Prexige
25 mg, oral, daily over 6 weeks
Other names: Vioxx
Time frame: 6 weeks
Looking for future studies?
Notify MeNovartis
Industry
A 6-Week Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled Parallel Group Clinical Saftey Study to Evaluate Incidence of Predefined Gastrointestinal Adverse Events and Peripheral Edema in Subjects With Primary Osteoarthritis Treated With COX189 400 mg o-do Using Rofecoxib 25 mg o.d. as a Comparator
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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