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Host and parasite factors influencing the pharmacokinetics of artesunate

Mitantragsteller Dr. Saadou Issifou
Fachliche Zuordnung Parasitologie und Biologie der Erreger tropischer Infektionskrankheiten
Förderung Förderung von 2010 bis 2015
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 164503726
 
Malaria is one of the most important infectious diseases. Due to drug-resistant parasites its chemotherapy remains a problem. Artesunate is a new antimalarial which could become the main antiparasitic agent especially against severe malaria. Three main aims will be pursuit: firstly, to investigate the best route of administration of artesunate, secondly the analysis of its pharmacokinetics compared to treatment outcome, and thirdly the investigation of patients and parasite polymorphisms leading to the individual variability of the pharmacokinetics in metabolizing artesunate. In this project three partners will combine their expertise to reach the proposed aims: The clinical part will take place at the Albert Schweitzer Hospital in Lambaréné, Gabon, which is a well-equipped and well-known site for clinical trials of the phases I-III. Pharmacokinetic parameters will be determined at the Institute for Clinical Pharmacology, parasite expression profiles will be determined at the Institute for Tropical Medicine in Tübingen and SNP arrays of human samples will be done at the Institute for Clinical Pharmacology. A very robust array technology will be installed at the Medical Research Unit in Lambaréné to analyse known polymorphisms in CYP2A6, UGT1A9, UGT2B7 and UGT2B7. At the end of the project we envisage a large data set that combines genetic and non-genetics parameters to answer crucial questions about the variability of pharmacokinetics in malaria treatment.
DFG-Verfahren Sachbeihilfen
Internationaler Bezug Gabun
Beteiligte Person Professor Dr. Matthias Schwab
Ehemaliger Antragsteller Professor Dr. Jürgen Kun, bis 6/2011 (†)
 
 

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