Marlene F.
- Country
- Portugal
- Department
- Medical Management
Research Overview
- Comparative Bioavailability and Bioequivalence of Oxazepam 10 mg Orodispersible Tablets (Test) Versus Seresta® 10 mg Tablets (Reference): A Single-Dose, Open-Label, Randomized, Two-Sequence, Two-Treatment, Two-Period Crossover Study in Healthy Subjects
- A Four Way Crossover Thorough QT/QTc Study to Evaluate the Electrocardiographic Effects of Therapeutic and Supratherapeutic Doses of Cytisinicline in Healthy Smokers
- Comparative Bioavailability and Bioequivalence of Oxazepam 50 mg Orodispersible Tablets (Test) Versus Seresta® 50 mg Tablets (Reference): A Single-Dose, Open-Label, Randomized, Two-Sequence, Two-Treatment, Two-Period Crossover Study in Healthy Subjects
Data & Insights
Has run more than one trial at 1 of 1 partner site.
Specializations
Bioequivalence Studies
The investigator specializes in conducting comparative bioavailability studies with a particular focus on orodispersible tablet formulations. Their research examines the therapeutic equivalence of different drug delivery systems, specifically investigating Oxazepam at various dosage strengths.
- Orodispersible tablet technologies
- Comparative pharmaceutical formulations
- Drug bioavailability assessment
Key interests include evaluating the performance of novel drug delivery systems against established reference products.
Addiction Medicine
The investigator conducts research in the field of nicotine addiction treatment, exploring innovative therapeutic approaches. Their work includes the evaluation of cytisinicline as a potential treatment option for smoking cessation.
- Smoking cessation therapies
- Addiction treatment assessment
- Therapeutic safety evaluation
The research encompasses cardiac safety assessments through QT/QTc studies of therapeutic compounds.
Clinical Pharmacology
The investigator's expertise extends to clinical pharmacology with emphasis on drug safety and efficacy evaluation. Their work includes comprehensive assessment of pharmaceutical compounds through thorough QT studies and other clinical endpoints.
- Drug safety assessment
- Pharmacological evaluation
- Clinical efficacy studies
Research focuses on establishing safety profiles of both therapeutic and supratherapeutic doses of investigational medications.
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