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PF 00299804

Known as: PF-299804, EGFR Inhibitor PF-00299804, PF-00299804-03 
A highly selective, small-molecule inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase with potential antineoplastic activity… 
National Institutes of Health

Papers overview

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2015
2015
Purpose: A secondary EGFR mutation, T790M, is the most common resistance mechanism in EGFR-mutant adenocarcinomas that have… 
2014
2014
TPS2110 Background: Recurrent GBM has a very poor prognosis and there is an unmet need for new treatment options. EGFR is an… 
2014
2014
Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA Background: Dacomitinib (D) is a highly selective… 
2012
2012
SummaryBiliary tract cancer (BTC) is associated with poor survival and unresponsiveness to chemotherapy. Targeted therapies for… 
2012
2012
Recently, HER2-directed treatment, such as trastuzumab, has shown clinical benefit in HER2-amplified gastric cancer. On the basis… 
2011
2011
5561 Background: PF is a potent, irreversible small molecule pan-HER tyrosine kinase inhibitor (TKI) with pre-clinical antitumor… 
2010
2010
7537 Background: Efficacy of gefitinib as first-line tx of adv NSCLC with epidermal growth factor receptor (EGFR) mutation (mu… 
2010
2010
3026 Background: Cross-talk between human epidermal growth factor receptor (HER) and insulin-like growth factor type I receptor… 
2010
2010
The 46th Annual Meeting of the American Society of Clinical Oncology, held in Chicago, included topics covering new therapeutic…