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Clinical Pharmacogenomics

Outcome of drug therapy is often variable, ranging from beneficial effects to lack of efficacy or serious adverse effects. The goal of clinical pharmacogenomic research is to determine how an individual’s genetic makeup controls the ways he or she responds to drugs – how the medications are absorbed, distributed in the body, broken down, eliminated – and to use that knowledge to determine the most suitable medication and the best possible dose for each patient. To meet the specific challenges of the complex nature of pharmacological responses, a comprehensive, integrative approach is needed looking into multifunctional networks of genes combining innovative study designs with novel biomarker technologies and pathbreaking –omics approaches (genomics, .transcriptomics, epigenomics).
 
 
 
 
 
 
 
Major Projects
  • Clinical pharmacology and pharmacogenetic /-genomic studies
  • Drug-Drug Interactions
  • Host pharmacogenomics of anti malaria therapy
  • Imaging Biomarker for Drug Transport
  • Clinical drug research
Dr. med. Reinhold Kerb

phone: ++49-711-8101 5767

Selected References
Original Articles
  • Nies AT, Koepsell H, Winter S, Burk O, Klein K, Kerb R, Zanger UM, Keppler D, Schwab M, Schaeffeler E (2009) Expression of organic cation transporters OCT1 (SLC22A1) and OCT3 (SCL22A3) is affected by genetic factors and cholestasis in human liver. Hepatology 50, 1227-1240.
  • Lang T, Haberl M, Jung D, Drescher A, Schlagenhaufer R, Keil A, Mornhinweg E, Stieger B, Kullak-Ublick GA, Kerb R (2006). Genetic variability, haplotype structures, and ethnic diversity of hepatic transporters MDR3 (ABCB4) and bile salt export pump (ABCB11). Drug Metab Dispos 34(9):1582-99.
  • Eap CB, Buclin T, Hustert E, Bleiber G, Golay KP, Aubert AC, Baumann P, Telenti A, Kerb R (2004). Pharmacokinetics of midazolam in CYP3A4- and CYP3A5-genotyped subjects. Eur J Clin Pharmacol; 60(4):231-6
  • Eap CB, Buclin T, Cucchia G, Zullino D, Hustert E, Bleiber G, Golay KP, Aubert AC, Baumann P, Telenti A, Kerb R (2004). Oral administration of a low dose of midazolam (75 microg) as an in vivo probe for CYP3A activity. Eur J Clin Pharmacol. 60(4):237
  • Pauli-Magnus C, Kerb R, Fattinger K, Lang T, Anwald B, Kullak-Ublick GA, Beuers U, Meier PJ (2004). BSEP and MDR3 haplotype structure in healthy Caucasians, primary biliary cirrhosis and primary sclerosing cholangitis. Hepatology 39(3):779-91
  • Siddiqui A, Kerb R, Weale ME, Brinkmann U, Smith A, Goldstein DB, Wood NW, and Sisodiya SM (2003). Association of multidrug resistance in epilepsy with a polymorphism in the drug-transporter ABCB1. N Engl J Med.; 348(15):1442-8.

Selected Reviews
  • Kerb R, Fux R, Mörike K, Kremsner PG, Gil JP, Gleiter CH, Schwab M. Pharmacogenetics of antimalarial drugs: effect on metabolism and transport. Lancet Infect Dis 2009;9(12):760-74
  • Kerb R. Implications of Genetic Polymorphisms in Drug Transporters for Pharmacotherapy. Cancer Letters 2006;234(1):4-33s

Curriculum Vitae Reinhold Kerb, MD

Affiliation
Senior Physician, Head Clinical Studies & Drug Information at the Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart and University of Tübingen

Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology
Auerbachstr. 112
D-70376 Stuttgart
phone: ++49-711-8101 5767
fax: ++49-711-859295
email: reinhold.kerb@ikp-stuttgart.de
Education and Professional Career
1982-1990 Study of medicine, Free University of Berlin
1992 State Licence as medical doctor
1998 MD (Dr. med.), Humboldt University of Berlin, Germany
2008 Board certificate as Clinical Pharmacologist
1991-1998 Research Associate, Institute of Clinical Pharmacology, University Medical Center Benjamin Franklin, University Medical Center Charité, Humboldt-University of Berlin.
1991-1992 Medical Residency, Institute of Clinical Pharmacology, University Medical Center Benjamin Franklin, University Medical Center Charité, Humboldt-University of Berlin.
1992-1994 Research Associate, Institute of Clinical Pharmacology, University Medical Center, Benjamin Franklin, University Medical Center Charité, Humboldt-University of Berlin.
1994-1998 Research Associate, Institute of Clinical Pharmacology, Charité, Humboldt-University, Germany.
1998-1999 Postdoctoral training, Institute of Clinical Pharmaology, Stanford University, California, USA.
2000-2001 Senior Scientist, Epidauros Biotechnologie AG, Bernried, Germany.
2001-2004 Department Head Pharmacogenetics, Epidauros Biotechnologie AG, Bernried, Germany.
2004-2007 Pharmacogenetics Advisor, Senior Clinical Scientist, AstraZeneca, Mölndal, Sweden.
Since 2007 Head Clinical Studies and Drug Information, IKP Stuttgart, Germany.
Professional Memberships
1999-present: American Association of Clinical Pharmacology and Therapeutics (ASCPT)
1997-present: Deutsche Gesellschaft für Klinische Pharmakologie und Therapie e.V. (DGKliPha)