Abstract
Levofloxacin is a bactericidal broad spectrum antibiotic against Gram-positive and Gram-negative pathogens. A randomized, two-treatment, two-period, two-way crossover study was conducted to evaluate the bioequivalence of Lectacin 250 mg tablet, a generic levofloxacin, to its reference drug, Cravit 250 mg tablet. Each period was separated by a 7-day washout. Serial blood samples were collected until 24 h after dosing and plasma levofloxacin concentrations were determined using a high performance liquid chromatography. Pharmacokinetic parameters were analyzed using K-BE Test 2007 and BA calc 2007 (Ministry of Food and Drug Safety, Cheongju-si, South Korea). The peak concentration (Cmax) and the area under the plasma concentration versus time curve from 0 to the last measurable concentration (AUC0-t) for the generic and reference levofloxacin were 4.48±0.89 mg/L and 4.46± 0.95 mg/L, and 25.33±4.12 mg∗h/L and 25.77±4.01 mg∗h/L, respectively, leading to a geometric mean ratio (90% confidence interval) of the generic to the reference levofloxacin of 1.0060 (0.9339–1.0842) and 0.9810 (0.9476–1.0159), respectively, for Cmax and AUC0-t. Lectacin 250 mg tablet is bioequivalent to Cravit 250 mg tablet.
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Table 1.
Table 2.
Characteristics | Values |
---|---|
Age (years) | 24.0±2.2 |
Height (cm) | 176.8±5.1 |
Body weight (kg) | 70.2±8.6 |
Table 3.
All values are presented as mean±SD [geometric mean], except for tmax, for which median (range) is presented. AUC0-t = area under the plasma concentration-time curve (AUC) from time 0 to 24 hours post dose; Cmax = peak plasma drug concentration; tmax = time to reach peak plasma concentration; Test = Lectacin 250 mg tablet; Reference = Cravit 250 mg tablet