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Study aim
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A randomized, open label, single dose, crossover, bioequivalence study of VITECT 200mg tablet of Actover Co., IRAN in comparison VFEND 200mg tablet of Pfizer in 24 healthy adult subjects under fasting condition
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Design
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A randomized, open label, single dose, crossover, bioequivalence study in 24 healthy subjects under fasting condition
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Settings and conduct
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This study is carried out in Core Research Center of ZAUMS located in Imam Ali Hospital in Zahedan. There is a separate space for sampling and forecasting emergency situations in order to accommodate and rest the volunteers. This crossover and open label study was performed on 24 healthy volunteers, which means that one group receives the first dose of the test and the second dose of the reference drug, and the other group receives the first dose of the reference and the second dose of the test drug.
The volunteers' health is verified by the project physician prior to entry into the study, and the volunteers' status is regularly monitored by the project physician on the day of drug administration. This study will be covered by insurance in order to compensate for any adverse effects.
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Participants/Inclusion and exclusion criteria
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Main Inclusion criteria: Healthy subjects aged between 18 -50 years old and weighted between 50 – 100 kg\\ Main exclusion criteria: Clinically relevant deviations from normal; Donation a unit of blood or participated in another clinical trial within the last three months; History of drug or alcohol abuse; Used any medication within 7- 14 days before the first treatment;
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Intervention groups
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Intervention: VITECT 200mg tablet, produced by Actover Co., (IRAN), single dose.
Control: VFEND 200mg tablet, produced by Pfizer company, single dose
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Main outcome variables
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Plasma concentration of voriconazol in plasma at 0 (before dosing), 0.5, 1.0, 1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 5.0, 6.0, 8.0, 10.0 & 24.0 hr. after dosing