Phase I and Pharmacodynamic Study of the Oral MEK Inhibitor CI-1040 in Patients With Advanced Malignancies
Author(s) -
Patricia LoRusso,
Alex A. Adjei,
Mary Varterasian,
Shirish M. Gadgeel,
Joel M. Reid,
David Mitchell,
Lorelei J. Hanson,
Pamela DeLuca,
Laura M. Bruzek,
Jill Piens,
Peggy Asbury,
Keri Van Becelaere,
Román Herrera,
Judith S. SeboltLeopold,
Mark B. Meyer
Publication year - 2005
Publication title -
journal of clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.482
H-Index - 548
eISSN - 1527-7755
pISSN - 0732-183X
DOI - 10.1200/jco.2005.14.415
Subject(s) - medicine , pharmacokinetics , pharmacodynamics , nausea , rash , vomiting , adverse effect , pharmacology , dosing , gastroenterology , cmax , response evaluation criteria in solid tumors , toxicity , maculopapular rash , kinase , phases of clinical research , microbiology and biotechnology , biology
This phase I study was undertaken to define the toxicity, pharmacokinetics, pharmacodynamics, maximum tolerated dose (MTD), and clinical activity of CI-1040, a small-molecule inhibitor of the dual-specificity kinases MEK(mitogen-activated protein kinase kinase) -1 and MEK2 , in patients with advanced malignancy.
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