Magdalena D.
- Country
- Poland
- Department
- Centrum Medyczne Pratia Katowice
Research Overview
- A Phase 3, Randomized, Double-blind, Active Comparator-controlled Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of V116 in Pneumococcal Vaccine-naïve Adults 18 to 64 years of Age With Increased Risk for Pneumococcal Disease
- Pan-European proof-of-concept study comparing Decentralised Clinical Trial (DCT) and hybrid approaches to conventional clinical trial approaches in patients with Type 2 diabetes mellitus treated with Toujeo®
Data & Insights
Has run more than one trial at 1 of 37 partner sites.
Specializations
Diabetes Management
This investigator specializes in Type 2 diabetes mellitus (T2DM) research, with particular focus on innovative treatment approaches and patient-centered care delivery models. Their work explores the effectiveness of decentralized clinical trials in diabetes management using medications like insulin glargine.
- Patient-centered diabetes care
- Remote monitoring systems
- Treatment adherence optimization
The research incorporates digital health technologies to enhance patient engagement and improve treatment outcomes in diabetes care.
Infectious Disease Prevention
The investigator conducts research in pneumococcal disease prevention, focusing on vaccine development and immunization strategies for at-risk adult populations. Their work examines novel vaccine formulations targeting specific pneumococcal serotypes.
- Vaccine immunogenicity
- Adult vaccination protocols
- Preventive medicine strategies
Their research emphasizes the evaluation of vaccine safety profiles and immune response measurements in adult populations.
Clinical Trial Innovation
The investigator explores hybrid clinical trial methodologies and their impact on research efficiency. Their work evaluates novel approaches to participant recruitment, retention, and diversity in clinical studies.
- Decentralized trial design
- Research cost optimization
- Data quality assessment
The research focuses on developing more accessible and efficient clinical trial models while maintaining high safety and data quality standards.
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