Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Karl Ernst Siegler"'
Publikováno v:
Clinical Pharmacology in Drug Development. 3:290-296
The pharmacokinetics of teneligliptin was compared in 3 groups of 8 subjects assigned according to their degree of hepatic impairment (mild, moderate, or matched healthy subjects). Hepatic impairment was associated with an increase in maximal plasma
Publikováno v:
Clinical Pharmacology in Drug Development. 2:246-254
The pharmacokinetics of teneligliptin was compared in renally impaired and healthy subjects. Subjects were assigned to one of four groups of eight subjects, according to the stage of disease [mild, moderate, severe or end stage renal disease (ESRD)],
Autor:
Laura Rabinovich-Guilatt, Asa Rembratt, Atef Halabi, Ofer Spiegelstein, Armin Schultz, Karl Ernst Siegler
Publikováno v:
British Journal of Clinical Pharmacology
Aim Pridopidine, a new oral drug for treatment of patients with motor symptoms associated with Huntington's Disease (HD) is currently under development. In steady-state conditions, pridopidine elimination is mediated primarily through renal excretion
Publikováno v:
Herz. 29:651-655
Der Einsatz von Glykoprotein-(GP-)IIb/IIIa-Inhibitoren hat in randomisierten Studien zu einer Verringerung der Rate ischamischer Komplikationen bei Patienten mit perkutaner koronarer Intervention (PCI) gefuhrt. Im vorliegenden prospektiven Register s
Publikováno v:
Clinical pharmacology in drug development. 3(4)
The pharmacokinetics of teneligliptin was compared in 3 groups of 8 subjects assigned according to their degree of hepatic impairment (mild, moderate, or matched healthy subjects). Hepatic impairment was associated with an increase in maximal plasma
Autor:
Atef, Halabi, Haidar, Maatouk, Karl Ernst, Siegler, Nadja, Faisst, Volkmar, Lufft, Norbert, Klause
Publikováno v:
Clinical pharmacology in drug development. 2(3)
The pharmacokinetics of teneligliptin was compared in renally impaired and healthy subjects. Subjects were assigned to one of four groups of eight subjects, according to the stage of disease [mild, moderate, severe or end stage renal disease (ESRD)],
Publikováno v:
BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy. 23(1)
Filgrastim XM02 is a biosimilar non-glycosylated recombinant methionyl form of human granulocyte colony-stimulating factor (r-MetHuG-CSF) expressed in Escherichia coli for subcutaneous and intravenous administration in the treatment of different form
Publikováno v:
Herz. 29(7)
The use of potent platelet inhibitors has been shown to reduce the rate of ischemic complications in patients with percutaneous coronary intervention (PCI) in randomized clinical trials. Eptifibatide is a small-molecule glycoprotein (GP) IIb/IIIa rec
Autor:
Jörg Rustige, Karlheinz Seidl, Ralf Zahn, Birgit Frilling, Klaus Dönges, Boris Fraiture, Torsten Becker, Jochen Senges, Karl Ernst Siegler, Bernd Mark
Publikováno v:
The American journal of cardiology. 89(4)
Risk factors for bleeding were found in varying rates in both groups of patients. Neither adjunctive heparin therapy nor risk factors for bleeding complications could sufficiently explain the significantly higher rates of peri-interventional bleeding
Autor:
Uwe Zeymer, Rudolf Schiele, Ricardo Seabra-Gomes, Anselm K. Gitt, Paolo M. Fioretti, Karl Ernst Siegler, David Hashdai, Jochen Senges, Jean-Pierre Bassand, Keith D. Dawkins, Martin Gottwik
Publikováno v:
Journal of the American College of Cardiology. 41:323