Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.
Skip to main content

Professor Joel Tarning

Professor Joel Tarning

Podcast Interview

Too high a dose can result in toxicity and side-effects, too low a dose can cause the illness to come back and at worse develop resistance. In the case of malaria, it is particularly important to get the dosage right for more vulnerable patients such as children and pregnant women. Professor Joel Tarning's findings have now been adopted by the World Health Organisation.

Social media

Joel Tarning

Professor of Clinical Pharmacology

Clinical Pharmacology

Joel Tarning is the head of the Clinical Pharmacology group focusing on bioanlytical method development, drug measurements in biological fluids and pharmacometric research. His research interest includes dose-optimisation using novel pharmacometric modelling approaches. His particular research interest includes antimalarial treatment in children and pregnant women.

The only way to determine accurately the correct dose regimens for antimalarial treatment is to establish a dose-response relationship through pharmacokinetic (PK) and pharmacodynamic (PD) modelling. Our research has shown that many of the antimalarial drugs developed in the past fifty years were introduced at the wrong dose, particularly in young children and pregnant women. This undoubtedly contributed to therapeutic failures and the development of drug-resistant parasites. Improving existing treatments and ensuring optimal dosing of the new drugs is essential for success in the control and elimination of malaria.

Joel Tarning received the biennial Giorgio Segré Prize from EUFEPS in 2014 for his research on the pharmacokinetic and pharmacodynamic properties of antimalarial drugs in vulnerable populations, such as pregnant women and young children.

Illustration of pharmacokinetic (PK) and pharmacodynamic (PD) modelling

Key publications

Recent publications

More publications