Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Josep-María Cendrós"'
Autor:
Concepción Peraire, Joaquim Ramis, Rosendo Obach, Iñaki F. Trocóniz, Josep-María Cendrós, María J. Garrido
Publikováno v:
The Journal of Clinical Pharmacology. 52:487-498
Acromegaly arises from excessive levels of growth hormone (GH), many of whose effects are mediated by stimulation of secretion of insulin-like growth factor 1 (IGF-1). Synthetic somatostatin analogues inhibit GH secretion. The objective of the study
Publikováno v:
Cancer Chemotherapy and Pharmacology. 63:945-952
Diflomotecan, a homocamptothecin, targets DNA topoisomerase I. Previous clinical trials have demonstrated a variable degree of dose limiting toxicity. The purpose of this study was to further evaluate the safety and pharmacokinetic profile of a range
Autor:
Iñaki F. Trocóniz, Rosendo Obach, Cristina Segura, Concepción Peraire, María J. Garrido, Josep-María Cendrós, Paola Principe
Publikováno v:
Cancer Chemotherapy and Pharmacology. 57:727-735
Purpose: To determine the maximum tolerated dose (MTD) of intravenous (iv) diflomotecan administered once every 3 weeks, and to characterize the relationship between pharmacokinetics and neutropenic effect, using a semi-mechanistic pharmacokinetic/ph
Publikováno v:
Veterinary Medicine and Science, Vol 8, Iss 1, Pp 31-45 (2022)
Abstract Enflicoxib is a newly developed NSAID of the coxib class. The optimal therapeutic dose to be confirmed in the field studies was established using a combination of pharmacokinetic (PK) modelling and pharmacodynamic (PD) studies. First, a PK s
Externí odkaz:
https://doaj.org/article/3964c3804fb44396812d9e5b21933afd
Autor:
Concepción Peraire, Nieves Velez de Mendizabal, Elba Romero, Emma Bascompta, Josep-María Cendrós, Iñaki F. Trocóniz, Rosendo Obach
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 342(3)
The objectives of the current work were to develop a predictive population pharmacokinetic (PK)/pharmacodynamic (PD) model for the testosterone (TST) effects of triptorelin (TRP) administered in sustained-release (SR) formulations to patients with pr
Autor:
Ron J. Keizer, Iñaki F. Trocóniz, Mats O. Karlsson, Elena Soto, Rosendo Obach, Lena E. Friberg, Jan H.M. Schellens, Concepción Peraire, Jos H. Beijnen, Josep María Cendrós, Alwin D. R. Huitema, Jantien Wanders
Publikováno v:
Investigational New Drugs
Summary In cancer chemotherapy neutropenia is a common dose-limiting toxicity. An ability to predict the neutropenic effects of cytotoxic agents based on proposed trial designs and models conditioned on previous studies would be valuable. The aim of
Autor:
Helena Colom, Dolors Soy, Josep Domenech, Concepción Peraire, Nuria Pardo, Rosa Farré, Josep-María Cendrós, Montserrat Torrent, Maria-Antonia Mangues
Publikováno v:
THERAPEUTIC DRUG MONITORING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
The goal of this study was to establish the population pharmacokinetics (PK) of high-dose methotrexate (HD-MTX) treatment in children with osteosarcoma and to explore the influence of patient covariates and between-occasion variability on drug dispos
Autor:
Paolo F. Boscani, María J. Garrido, Joaquiln Ramis, Iñaki F. Trocóniz, Rosendo Obach, Concepción Peraire, Josep-María Cendrós
Publikováno v:
Clinical pharmacokinetics. 48(1)
Lanreotide is a somatostatin analogue used for the treatment of acromegaly and neuroendocrine tumours. The objective of this study was to develop a pharmacokinetic model for the sustained-release formulation lanreotide Autogel after deep subcutaneous
Autor:
A. Leselbaum, Joaquim Ramis, Nina R. C. Musolino, Raquel S. Jallad, F. Catus, Josep-María Cendrós, Marcello D. Bronstein, Rosendo Obach
Publikováno v:
Clinical endocrinology. 63(5)
Summary Objective To investigate the pharmacokinetic profile of a prolonged release, aqueous Autogel® formulation of the somatostatin analogue lanreotide (Lan-ATG). Design A phase II, randomized, double-blind study, during which patients received 60