The purpose of this study is to evaluate pharmacokinetics, safety and tolerability profile of BZ371A topically administered in healthy patients.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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