EACPT 2024 Rotterdam – Precision Clinical Pharmacology
Please check the abstract submission guidelines before uploading your abstract.
Aim of therapy
Monitoring outcome and compliance
Pathophysiology; drug discovery; mechanism of action; mechanism of toxicity; (epi)genetics of disease; target finding; lead optimization.
Modulation of the target; target engagement; animal or human models of disease; pharmacokinetics and drug metabolism; entry-into-human; human proof of mechanism and proof-of-concept.
Active-controlled clinical trials on drug efficacy and/or safety; trial methodology; regulatory sciences.
Patient-tailored pharmacotherapy; pharmacogenetics in drug efficacy and/or drug safety; drug-drug interaction; drug therapy in organ impairment; demographics and/or ethnicities in pharmacotherapy.
Drug therapy selection after passing Steps 1-4; cost-efficacy; drug treatment guidelines; rational prescribing; shared decision making; health technology assessment; therapeutic practices; formulary optimization; prescription review; learning healthcare.
Patient follow-up; (remote) monitoring of efficacy and safety; real world data; pharmacovigilance; therapeutic drug monitoring; compliance; treatment adaptation & optimization.
Please check the Abstract submission guidelines before uploading your abstract.
The abstract should not exceed 500 words including spaces and punctuation. The abstract title is included in the overall character count. The abstract must be structured in the following five specified subtitles: Introduction, Objectives, Methods, Results and Conclusion.
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