Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jasper Dingemanse

Showing results (201-210 of 238) with videos related to

Pageof 24
Sort By:
British Journal of Clinical Pharmacology|August 24, 2022
Multiple-ascending doses of ACT-1014-6470, an oral complement factor 5a receptor 1 (C5a<sub>1</sub> receptor) antagonist: Tolerability, pharmacokinetics and target engagementMarion Anliker-Ort, Jasper Dingemanse, Hervé Farine, et al.
Journal of Cardiovascular Pharmacology|October 16, 2013
Tolerability and pharmacokinetics of ACT-280778, a novel nondihydropyridine dual L/T-type calcium channel blocker: early clinical studies in healthy male subjects using adaptive designsMarkus S Mueller, Kasra Shakeri-Nejad, Marcelo M Gutierrez, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 23, 2013
Elucidation of the metabolic pathways and the resulting multiple metabolites of almorexant, a dual orexin receptor antagonist, in humansJasper Dingemanse, Petra Hoever, Matthias Hoch, et al.
Clinical Pharmacology and Therapeutics|July 13, 2017
Lucerastat, an Iminosugar for Substrate Reduction Therapy: Tolerability, Pharmacodynamics, and Pharmacokinetics in Patients With Fabry Disease on Enzyme ReplacementNicolas Guérard, Daniel Oder, Peter Nordbeck, et al.
The AAPS Journal|December 23, 2011
Effect of cyclosporine and rifampin on the pharmacokinetics of macitentan, a tissue-targeting dual endothelin receptor antagonistShirin Bruderer, Päivi Aänismaa, Marie-Claude Homery, et al.
Journal of Clinical Pharmacology|February 7, 2015
A novel CRTH2 antagonist: Single- and multiple-dose tolerability, pharmacokinetics, and pharmacodynamics of ACT-453859 in healthy subjectsMartine Géhin, Daniel S Strasser, Jochen Zisowsky, et al.
Pharmacology Research & Perspectives|July 20, 2023
Modeling time-delayed concentration-QT effects with ACT-1014-6470, a novel oral complement factor 5a receptor 1 (C5a<sub>1</sub> receptor) antagonistMarion Anliker-Ort, Chih-Hsuan Hsin, Andreas Krause, et al.
British Journal of Clinical Pharmacology|September 27, 2023
Pharmacokinetics, pharmacodynamics and safety of the novel C-X-C chemokine receptor 3 antagonist ACT-777991: Results from the first-in-human study in healthy adultsMarie-Laure Boof, Martine Géhin, Christine Voors-Pette, et al.
Clinical Pharmacokinetics|December 23, 2015
Pharmacokinetic/Pharmacodynamic Modelling of Receptor Internalization with CRTH2 Antagonists to Optimize Dose SelectionAndreas Krause, Jochen Zisowsky, Daniel S Strasser, et al.
Scientific Reports|March 12, 2020
Ensemble modeling highlights importance of understanding parasite-host behavior in preclinical antimalarial drug developmentLydia Burgert, Matthias Rottmann, Sergio Wittlin, et al.
Pageof 24

Showing results (201-210 of 238) with videos related to

Sort By:
Pageof 24
British Journal of Clinical Pharmacology|August 24, 2022
Multiple-ascending doses of ACT-1014-6470, an oral complement factor 5a receptor 1 (C5a<sub>1</sub> receptor) antagonist: Tolerability, pharmacokinetics and target engagementMarion Anliker-Ort, Jasper Dingemanse, Hervé Farine, et al.
Journal of Cardiovascular Pharmacology|October 16, 2013
Tolerability and pharmacokinetics of ACT-280778, a novel nondihydropyridine dual L/T-type calcium channel blocker: early clinical studies in healthy male subjects using adaptive designsMarkus S Mueller, Kasra Shakeri-Nejad, Marcelo M Gutierrez, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 23, 2013
Elucidation of the metabolic pathways and the resulting multiple metabolites of almorexant, a dual orexin receptor antagonist, in humansJasper Dingemanse, Petra Hoever, Matthias Hoch, et al.
Clinical Pharmacology and Therapeutics|July 13, 2017
Lucerastat, an Iminosugar for Substrate Reduction Therapy: Tolerability, Pharmacodynamics, and Pharmacokinetics in Patients With Fabry Disease on Enzyme ReplacementNicolas Guérard, Daniel Oder, Peter Nordbeck, et al.
The AAPS Journal|December 23, 2011
Effect of cyclosporine and rifampin on the pharmacokinetics of macitentan, a tissue-targeting dual endothelin receptor antagonistShirin Bruderer, Päivi Aänismaa, Marie-Claude Homery, et al.
Journal of Clinical Pharmacology|February 7, 2015
A novel CRTH2 antagonist: Single- and multiple-dose tolerability, pharmacokinetics, and pharmacodynamics of ACT-453859 in healthy subjectsMartine Géhin, Daniel S Strasser, Jochen Zisowsky, et al.
Pharmacology Research & Perspectives|July 20, 2023
Modeling time-delayed concentration-QT effects with ACT-1014-6470, a novel oral complement factor 5a receptor 1 (C5a<sub>1</sub> receptor) antagonistMarion Anliker-Ort, Chih-Hsuan Hsin, Andreas Krause, et al.
British Journal of Clinical Pharmacology|September 27, 2023
Pharmacokinetics, pharmacodynamics and safety of the novel C-X-C chemokine receptor 3 antagonist ACT-777991: Results from the first-in-human study in healthy adultsMarie-Laure Boof, Martine Géhin, Christine Voors-Pette, et al.
Clinical Pharmacokinetics|December 23, 2015
Pharmacokinetic/Pharmacodynamic Modelling of Receptor Internalization with CRTH2 Antagonists to Optimize Dose SelectionAndreas Krause, Jochen Zisowsky, Daniel S Strasser, et al.
Scientific Reports|March 12, 2020
Ensemble modeling highlights importance of understanding parasite-host behavior in preclinical antimalarial drug developmentLydia Burgert, Matthias Rottmann, Sergio Wittlin, et al.
Pageof 24