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Clinical Trial Summary

To assess the impact of prophylactic treatment on the incidence of adverse events in advanced NSCLC patients (post chemotherapy) treated with dacomitinib daily as a single agent. To assess the impact of an interrupted dacomitinib dosing schedule in Cycle 1 on the incidence of adverse events in first-line advanced NSCLC patients with an EGFR mutation (HER-1 mutation, HER-2 mutation or HER-2 amplification).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01465802
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 2
Start date December 26, 2011
Completion date May 18, 2015

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