Drug intelligence / Profile preview

dacomitinib + antacid

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral
01

Overview

This is a combination of dacomitinib, an oral irreversible small molecule inhibitor of the human epidermal growth factor receptor (EGFR) family (including EGFR/HER1, HER2, and HER4) tyrosine kinases, and an antacid. Dacomitinib is primarily indicated as first-line treatment for patients with metastatic non-small cell lung cancer (NSCLC) harboring specific EGFR mutations. The addition of an antacid may be considered in clinical practice to manage gastrointestinal symptoms or acid-related side effects; however, coadministration can affect drug absorption due to pH-dependent solubility. Clinical data show that short-acting antacids do not significantly alter dacomitinib exposure if administered at least 6 hours before or 10 hours after the kinase inhibitor[2][3][6]. This combination should not be confused with fixed-dose combinations; it refers to concurrent use.

02

Targets

ERBB4 (Erb-b2 receptor tyrosine kinase 4)EGFR T790M (Epidermal growth factor receptor T790M mutant)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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