Jiří G.
- Country
- Czechia
- Department
- Clinical Unit
Research Overview
- Bioavailability Study of Rosuvastatin/Ezetimibe and Nilemdo Versus Nustendi and Crestor in Healthy Subjects Under Fasting Conditions
- Assessment of the Relative Bioavailability of Rotigotine 4.5 mg Transdermal Patch Versus Neupro 2 mg/24 h Patch in Healthy Adults Under Fasting Conditions
- Comparative Bioavailability Study of Amlodipine/Valsartan/Hydrochlorothiazide Versus Reference in Healthy Subjects Under Fasting Conditions
Data & Insights
Has run more than one trial at 1 of 3 partner sites.
Specializations
Bioequivalence Studies
This investigator specializes in conducting bioequivalence and bioavailability studies with a focus on comparing novel drug formulations to established reference products.
- Oral medications assessment
- Transdermal delivery systems
- Drug formulation comparisons
The research encompasses both single-dose and multiple-dose administration protocols in healthy volunteers.
Drug Delivery Systems
The investigator evaluates various pharmaceutical delivery mechanisms, including innovative formulation technologies and alternative administration routes.
- Oral suspensions
- Transdermal patches
- Tablet formulations
Studies include assessment of both immediate and extended-release formulations under different physiological conditions.
Clinical Pharmacology
Expertise in pharmacokinetic assessment of various therapeutic compounds, with particular attention to drug-drug interactions and food effects.
- Cardiovascular medications
- Antiviral agents
- Combination drug products
Research includes evaluation of both single-component and fixed-dose combination products.
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