Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jacqueline H M, van Kuijk"'
Autor:
André M. M. Miltenburg, Marita Prohn, Renger G. Tiessen, Jacqueline H. M. van Kuijk, Martin de Kort, Rob J. W. Berg
Publikováno v:
British Journal of Clinical Pharmacology. 75:1221-1230
Aim Conjugation to antithrombin III ATIII-binding pentasaccharides has been proposed as a novel method to extend the half-life of therapeutic proteins. We aim to validate this technological concept in man by performing a first-in-human study using Ca
Autor:
Jacqueline H. M. van Kuijk, Pierre A. M. Peeters, Pieter-Jan de Kam, T. Thomsen, Marita Prohn
Publikováno v:
Clinical Drug Investigation. 30:599-611
Sugammadex reverses the effects of rocuronium- and vecuronium-induced neuromuscular blockade, which are achieved by encapsulation. It is known that some non-antiarrhythmic drugs have the potential to delay cardiac repolarization and it is therefore r
Autor:
Benoit Plaud, Olli A. Meretoja, Yvonne Hermens, Rainer Hofmockel, Julien Raft, Peter A. Stoddart, Jacqueline H. M. van Kuijk, Rajinder K. Mirakhur
Publikováno v:
Anesthesiology. 110:284-294
Background: Sugammadex reverses neuromuscular blockade by chemical encapsulation of rocuronium. This phase IIIA study explored efficacy and safety of sugammadex in infants (28 days to 23 months), children (2‐11 yr), adolescents (12‐17 yr), and ad
Autor:
Jacqueline H. M. van Kuijk, Robert I McLachlan, Aleksander Giwercman, Ann J. Conway, Gerrit Voortman, Pierre Bouloux, Gordon H.W. Baker, Leo Turner, Annemarie Syska, David J. Handelsman, Henry G. Burger, Eberhard Nieschlag, Robert Ochsenkuehn, Niels E. Skakkebæk, Frederick C. W. Wu
Publikováno v:
Journal of Andrology. 24:604-611
A multicenter, open-label, randomized efficacy and safety study was performed with combined human chorionic gonadotropin (hCG) and recombinant follicle-stimulating hormone (recFSH) (Puregon(R)) treatment to induce spermatogenesis in hypogonadotropic
Publikováno v:
International journal of clinical pharmacology and therapeutics. 50(8)
Objective Sugammadex is a novel γ-cyclodextrin and the first selective relaxant binding agent to be developed for the reversal of rocuronium and vecuroniuminduced neuromuscular blockade. According to International Conference on Harmonization (ICH) E
Autor:
André M M, Miltenburg, Marita, Prohn, Jacqueline H M, van Kuijk, Renger G, Tiessen, Martin, de Kort, Rob J W, Berg
Publikováno v:
British journal of clinical pharmacology. 75(5)
Conjugation to antithrombin III ATIII-binding pentasaccharides has been proposed as a novel method to extend the half-life of therapeutic proteins. We aim to validate this technological concept in man by performing a first-in-human study using CarboC