Research Topics
| Joachim StangierSummaryAffiliation: Boehringer Ingelheim Publications
| Collaborators
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Detail Information
Publications
Using the HEMOCLOT direct thrombin inhibitor assay to determine plasma concentrations of dabigatranJoachim Stangier
Drug Metabolism and Pharmacokinetics, Boehringer Ingelheim Pharma GmbH and Co KG, Biberach an der Riss, Germany
Blood Coagul Fibrinolysis 23:138-43. 2012..The use of this rapid, established, standardized and calibrated assay should provide accurate and consistent results when assessing the anticoagulant activity of dabigatran...
Influence of renal impairment on the pharmacokinetics and pharmacodynamics of oral dabigatran etexilate: an open-label, parallel-group, single-centre studyJoachim Stangier
Boehringer Ingelheim Pharma GmbH and Co KG, Biberach, Germany
Clin Pharmacokinet 49:259-68. 2010..A decrease in the dose and/or an increase in the administration interval in these patients may be appropriate. In patients with ESRD, dabigatran can be partly removed from the plasma by haemodialysis...
Pharmacology, pharmacokinetics, and pharmacodynamics of dabigatran etexilate, an oral direct thrombin inhibitorJoachim Stangier
Department of Drug Metabolism and Pharmacokinetics, Boehringer Ingelheim Pharma GmbH and Co KG, Birkendorfer Strasse, Biberach an der Riss, Germany
Clin Appl Thromb Hemost 15:9S-16S. 2009....
Coadministration of dabigatran etexilate and atorvastatin: assessment of potential impact on pharmacokinetics and pharmacodynamicsJoachim Stangier
Boehringer Ingelheim Pharma GmbH and Co KG, Biberach an der Riss, Germany
Am J Cardiovasc Drugs 9:59-68. 2009....
Clinical pharmacokinetics and pharmacodynamics of the oral direct thrombin inhibitor dabigatran etexilateJoachim Stangier
Boehringer Ingelheim Pharma GmbH and Co KG, Biberach, Germany
Clin Pharmacokinet 47:285-95. 2008....
Pharmacokinetics and pharmacodynamics of the direct oral thrombin inhibitor dabigatran in healthy elderly subjectsJoachim Stangier
Boehringer Ingelheim Pharma GmbH and Co KG, Biberach, Germany
Clin Pharmacokinet 47:47-59. 2008....
The pharmacokinetics, pharmacodynamics and tolerability of dabigatran etexilate, a new oral direct thrombin inhibitor, in healthy male subjectsJoachim Stangier
Boehringer Ingelheim Pharma GmbH and Co KG, Ingelheim, Germany
Br J Clin Pharmacol 64:292-303. 2007..Two double-blind, randomized trials were undertaken to investigate the pharmacokinetics (PK), pharmacodynamics (PD) and tolerability of orally administered dabigatran etexilate in healthy male subjects...
Dabigatran etexilate--a novel, reversible, oral direct thrombin inhibitor: interpretation of coagulation assays and reversal of anticoagulant activityJoanne van Ryn
Department of Drug Discovery Support, Boehringer Ingelheim Pharma GmbH and Co KG, Biberach an der Riss, Germany
Thromb Haemost 103:1116-27. 2010....
Pharmacokinetic profile of the oral direct thrombin inhibitor dabigatran etexilate in healthy volunteers and patients undergoing total hip replacementJoachim Stangier
Department of Drug Metabolism and Pharmacokinetics, Boehringer Ingelheim Pharma GmbH and Co KG, Birkendorfer Strasse, Biberach an der Riss, D-88397, Germany
J Clin Pharmacol 45:555-63. 2005..These pharmacokinetic characteristics confirm the suitability of this oral solid dosage form for use in future clinical trials...
Twice daily dosing of dabigatran for stroke prevention in atrial fibrillation: a pharmacokinetic justificationAndreas Clemens
Boehringer Ingelheim Pharma GmbH and Co KG, Ingelheim, Germany
Curr Med Res Opin 28:195-201. 2012..Based on its pharmacokinetic profile, dabigatran is dosed twice daily. This analysis provides a quantitative rationale for the selection of the dose regimen in this population...
Pharmacokinetics and pharmacodynamics in Japanese and Caucasian subjects after oral administration of dabigatran etexilateSebastian Hartter
Translational Medicine, Boehringer Ingelheim Pharma GmbH and Co KG, Biberach, Germany
Thromb Haemost 107:260-9. 2012....
The metabolism and disposition of the oral direct thrombin inhibitor, dabigatran, in humansStefan Blech
Boehringer Ingelheim Pharma GmbH and Co KG, Department of Drug Metabolism and Pharmacokinetics, Biberach, Germany
Drug Metab Dispos 36:386-99. 2008..o. administration of dabigatran etexilate and that the potential for clinically relevant interactions between dabigatran and drugs metabolized by cytochrome P450 is low...
Population pharmacokinetic analysis of the new oral thrombin inhibitor dabigatran etexilate (BIBR 1048) in patients undergoing primary elective total hip replacement surgeryInaki F Troconiz
Boehringer Ingelheim Pharma GmbH and Co KG, Birkendorfer Strasse 68, 88397 Biberach, Germany
J Clin Pharmacol 47:371-82. 2007..As a consequence, the rate of absorption is reduced and interindividual variability in drug exposure increased. On the following days, the disposition in plasma of BIBR 953 ZW is less variable...
Dabigatran with or without concomitant aspirin compared with warfarin alone in patients with nonvalvular atrial fibrillation (PETRO Study)Michael D Ezekowitz
Lankenau Institute for Medical Research and The Heart Center, Wynnewood, PA, USA
Am J Cardiol 100:1419-26. 2007..The 2 highest doses of dabigatran suppress D-dimer concentrations. Serious liver toxicity was not seen. The significance of the increase of DTB2 concentrations in dabigatran-treated patients needs resolution...
Effects of the direct thrombin inhibitor dabigatran on ex vivo coagulation time in orthopaedic surgery patients: a population model analysisKarl-Heinz Liesenfeld
Boehringer Ingelheim Pharma GmbH and Co, KG, Ingelheim, Germany
Br J Clin Pharmacol 62:527-37. 2006..Blood coagulation prolongation was most pronounced following surgery. Data suggest that ECT provides a more precise description of the anticoagulant effect than aPTT...
In vitro and in vivo characterization of the activity of telmisartan: an insurmountable angiotensin II receptor antagonistMarc P Maillard
Division of Hypertension and Vascular Medicine, University Hospital of Lausanne, CHUV CH 1011 Lausanne, Switzerland
J Pharmacol Exp Ther 302:1089-95. 2002..Taken together, our in vitro data show that the insurmountable antagonism of telmisartan is due at least in part to its very slow dissociation from AT1 receptors...
