Study to investigate the bioequivalence between 10 mg tablets (test drug) and 10 mg capsules (reference drug) of meloxicam (UHAC 62 XX) after 7-day administration.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Cmax (maximum observed concentration of the analyte in plasma)
Time frame: up to day 8
AUC 0-τ (Area under the concentration time curve in plasma from zero time to 24 hours after 7-day administration)
Time frame: up to day 8
Tmax (Time to reach Cmax)
Time frame: up to day 8
T1/2 (Terminal half-life in plasma)
Time frame: up to day 8
MRT 0-τ (Mean residence time in the body after 7-day administration)
Time frame: up to day 8
Cτ (Concentration of the analyte in plasma 24 hours after 7-day administration)
Time frame: up to day 8
Number of patients with adverse events
Time frame: up to 20 days after final administration
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