The purpose of this study is to evaluate pharmacokinetics, safety and tolerability profile of BZ371A topically administered in healthy patients.
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Cmax
Timeframe: 0 (Pre-dose), 15, 30, 60, 180 and 360 minutes post dose
T1/2
Timeframe: 0 (Pre-dose), 15, 30, 60, 180 and 360 minutes post dose
AUC
Timeframe: 0 (Pre-dose), 15, 30, 60, 180 and 360 minutes post dose
Clearance (CL)
Timeframe: 0 (Pre-dose), 15, 30, 60, 180 and 360 minutes post dose
Vd
Timeframe: 0 (Pre-dose), 15, 30, 60, 180 and 360 minutes post dose
Adverse Effects Evaluation
Timeframe: All adverse effect will be collected from the beginning of the study up to one week after drug administration
Physical Exam
Timeframe: Baseline and 1 week
Change in SBP
Timeframe: Baseline and 1 week
Change in DBP
Timeframe: Baseline and 1 week
Change in Heart Rate
Timeframe: Baseline and 1 week
Change in Respiratory Rate
Timeframe: Baseline and 1 week
Change in Temperature
Timeframe: Baseline and 1 week
Basal Chest Electrocardiogram (ECG)
Timeframe: Baseline and 1 week
Blood Evaluation
Timeframe: Baseline and 1 day
Urine Evaluation
Timeframe: Baseline and 1 week