Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gholamreza Rahmanzadeh"'
Autor:
Xiaoming, Cui, Xinhui, Chen, Nathalie, Pognan, Tirtha, Sengupta, Gholamreza, Rahmanzadeh, Ruediger, Kornberger, Monica, Giovannini
Publikováno v:
The Journal of Clinical Pharmacology. 63:228-238
Capmatinib is a highly specific, potent, and selective mesenchymal-epithelial transition factor inhibitor predominantly eliminated by cytochrome P450 (CYP) 3A4 and aldehyde oxidase. Here, we investigated the effects of a strong CYP3A inhibitor (itrac
Autor:
Xinhui Chen, Nicolas Isambert, Rafael López‐López, Monica Giovannini, Nathalie Pognan, Shruti Kapoor, Michelle Quinlan, Benoit You, Xiaoming Cui, Gholamreza Rahmanzadeh, Morten Mau‐Sorensen
Publikováno v:
Chen, X, Isambert, N, López-López, R, Giovannini, M, Pognan, N, Kapoor, S, Quinlan, M, You, B, Cui, X, Rahmanzadeh, G & Mau-Sorensen, M 2023, ' Effect of capmatinib on the pharmacokinetics of substrates of CYP3A (midazolam) and CYP1A2 (caffeine) in patients with MET-dysregulated solid tumours ', British Journal of Clinical Pharmacology, vol. 89, no. 3, pp. 1046-1055 . https://doi.org/10.1111/bcp.15544
Background: Preclinical studies showed that capmatinib reversibly inhibits cytochrome P450 (CYP) 3A4 and CYP1A2 in a time-dependent manner. In this study, we evaluated the effect of capmatinib on the exposure of sensitive substrates of CYP3A (midazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e751618123039bf7c0a8151dbb589a3e
https://curis.ku.dk/portal/da/publications/effect-of-capmatinib-on-the-pharmacokinetics-of-substrates-of-cyp3a-midazolam-and-cyp1a2-caffeine-in-patients-with-metdysregulated-solid-tumours(72512f3f-33d1-4b5e-974b-4b8e0ef1d394).html
https://curis.ku.dk/portal/da/publications/effect-of-capmatinib-on-the-pharmacokinetics-of-substrates-of-cyp3a-midazolam-and-cyp1a2-caffeine-in-patients-with-metdysregulated-solid-tumours(72512f3f-33d1-4b5e-974b-4b8e0ef1d394).html
Autor:
Gholamreza Rahmanzadeh, Eddie Marriere, Xinhui Chen, Giuseppe Curigliano, Monica Giovannini, Philippe Pultar, Xiaoming Cui, Enrique Grande, Michelle Quinlan
Publikováno v:
British Journal of Clinical Pharmacology. 87:2867-2878
Aims Capmatinib, an orally bioavailable, highly potent and selective MET inhibitor, was recently approved to treat adult patients with metastatic nonsmall cell lung cancer with METex14 skipping mutations. The study investigated the effect of capmatin
Autor:
Regine Hansen, Yi Jin, Kirsten Schroer, Sylvia Zhao, Gian Camenisch, Hubert Borell, Gholamreza Rahmanzadeh, Jan Jaap van Lier, Axel Meissner, Ulrike Pfaar, Ulrike Glaenzel
Publikováno v:
Drug Metabolism and Disposition. 48:873-885
Capmatinib (INC280), a highly selective and potent inhibitor of the MET receptor tyrosine kinase, has demonstrated clinically meaningful efficacy and a manageable safety profile in patients with advanced non-small-cell lung cancer harboring MET exon
Autor:
Xinhui Chen, Michelle Quinlan, Shruti Kapoor, Xiaoming Cui, Thomas Marbury, Nathalie Pognan, Gholamreza Rahmanzadeh, Monica Giovannini
Publikováno v:
British journal of clinical pharmacology. 88(1)
Capmatinib, a mesenchymal-epithelial transition factor tyrosine kinase inhibitor, is metabolized by cytochrome P450 (CYP) 3A4 and aldehyde oxidase. In individuals with hepatic impairment, alterations in hepatobiliary excretion and metabolism could le
Autor:
Enrique, Grande, Monica, Giovannini, Eddie, Marriere, Philippe, Pultar, Michelle, Quinlan, Xinhui, Chen, Gholamreza, Rahmanzadeh, Giuseppe, Curigliano, Xiaoming, Cui
Publikováno v:
British Journal of Clinical Pharmacology
Aims Capmatinib, an orally bioavailable, highly potent and selective MET inhibitor, was recently approved to treat adult patients with metastatic nonsmall cell lung cancer with METex14 skipping mutations. The study investigated the effect of capmatin
Autor:
Meredith Cain, Birk Poller, H. Markus Weiss, Swarupa Kulkarni, Gholamreza Rahmanzadeh, Janardhana Vemula, Thomas Langenickel, Bharti Shah
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 49(5)
Fevipiprant, an oral, nonsteroidal, highly selective, reversible, and competitive prostaglandin D2 receptor 2 antagonist, is eliminated by glucuronidation and by direct renal excretion predominantly via organic anion transporter (OAT) 3. This study a
Autor:
Bharti Shah, Anton Drollmann, Cathy Gray, Erin Greco, Gholamreza Rahmanzadeh, Markus Weiss, Imad Hanna, Birk Poller, Swarupa Kulkarni
Publikováno v:
Pulmonary Pharmacology & Therapeutics. 72:102097
Autor:
Veit J. Erpenbeck, Gholamreza Rahmanzadeh, Meredith Cain, Markus Weiss, Swathi Mandalapu, Janardhana Vemula, Kayoko Matsumoto, Michelle Ababa, Ravish Bhuyan
Publikováno v:
Airway Pharmacology and Treatment.
Introduction: Fevipiprant, an oral prostaglandin D2 receptor 2 (DP2/CRTh2) antagonist, is in clinical development for treatment of allergic conditions. We assessed safety, tolerability and pharmacokinetics (PK) after high single and multiple doses of