A phase I dose-escalation and bioavailability study of oral and intravenous formulations of erlotinib (Tarceva®, OSI-774) in patients with advanced solid tumors of …

M Ranson, H Shaw, J Wolf, M Hamilton… - Cancer chemotherapy …, 2010 - Springer
Purpose An intravenous (IV) erlotinib formulation has not been characterized in cancer
patients but may be useful in those with gastrointestinal abnormalities that impact on the …

Phase I dose-finding and pharmacokinetic study of the oral epidermal growth factor receptor tyrosine kinase inhibitor Ro50-8231 (erlotinib) in Japanese patients with …

N Yamamoto, A Horiike, Y Fujisaka… - Cancer chemotherapy …, 2008 - Springer
Purpose The objectives of this phase I dose-finding study of erlotinib were to investigate the
toxicity profile, to confirm the acceptable toxicity of doses up to 150 mg/day, and to assess …

Pharmacokinetics and pharmacodynamics: maximizing the clinical potential of Erlotinib (Tarceva)

M Hidalgo, D Bloedow - Seminars in oncology, 2003 - Elsevier
Pharmacokinetic and pharmacodynamic studies have an important role in the optimization
of targeted agents. Phase I pharmacokinetic studies show that treatment with erlotinib HCl …

Phase I, pharmacokinetic, and biological study of erlotinib in combination with paclitaxel and carboplatin in patients with advanced solid tumors

A Patnaik, D Wood, AW Tolcher, M Hamilton… - Clinical cancer …, 2006 - AACR
Purpose: To assess the feasibility of administering erlotinib, an inhibitor of epidermal growth
factor receptor (EGFR) tyrosine kinase, in combination with paclitaxel and carboplatin, and …

Preclinical studies with erlotinib (Tarceva)

RW Akita, MX Sliwkowski - Seminars in oncology, 2003 - Elsevier
Erlotinib HCl (Tarceva; Genentech, Inc, South San Francisco, CA) is an orally available,
highly selective, reversible inhibitor of epidermal growth factor receptor (HER1/EGFR) …

Erlotinib: another candidate for the therapeutic drug monitoring of targeted therapy of cancer? A pharmacokinetic and pharmacodynamic systematic review of literature

E Petit-Jean, T Buclin, M Guidi, E Quoix… - Therapeutic drug …, 2015 - journals.lww.com
Erlotinib is currently marketed at fixed standard dosage against pancreatic cancer and non–
small-cell lung carcinoma. However, erlotinib pharmacokinetics (PK) is characterized by …

Clinical pharmacokinetics of erlotinib in patients with solid tumors and exposure‐safety relationship in patients with non–small cell lung cancer

JF Lu, SM Eppler, J Wolf, M Hamilton… - Clinical …, 2006 - Wiley Online Library
Objective Our objective was to assess the pharmacokinetics of erlotinib in a large patient
population with solid tumors, identify covariates, and explore relationships between …

Phase 1b dose escalation study of erlotinib in combination with infusional 5-Fluorouracil, leucovorin, and oxaliplatin in patients with advanced solid tumors

AR Hanauske, J Cassidy, J Sastre, C Bolling… - Clinical cancer …, 2007 - AACR
Abstract Purpose: Erlotinib (Tarceva) is a potent epidermal growth factor receptor (HER1)
inhibitor. Infusional 5-fluorouracil (5-FU), leucovorin, and oxaliplatin (FOLFOX) is a standard …

Phase I and pharmacokinetic study of erlotinib for solid tumors in patients with hepatic or renal dysfunction: CALGB 60101

AA Miller, DJ Murry, K Owzar, DR Hollis… - Journal of clinical …, 2007 - ascopubs.org
Purpose We investigated dose and pharmacokinetics of erlotinib in patients with hepatic
dysfunction or renal dysfunction. Patients and Methods Patients were assigned to one of …

Effect of gastric pH on erlotinib pharmacokinetics in healthy individuals: omeprazole and ranitidine

H Kletzl, M Giraudon, PS Ducray, M Abt… - Anti-cancer …, 2015 - journals.lww.com
The aim of this study was to evaluate the effect of coadministration of acid-reducing agents
on the pharmacokinetic exposure of orally administered epidermal growth factor receptor …