Drug intelligence / Profile preview

celecoxib + gefitinib

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

Overview

Celecoxib + gefitinib is a combination of two small molecule drugs used experimentally in oncology. Celecoxib is a selective cyclooxygenase-2 (COX-2) inhibitor, while gefitinib is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. This combination has been studied for its potential to enhance antitumor effects by simultaneously inhibiting COX-2-mediated inflammation and EGFR-driven cell proliferation and survival pathways. Early-phase clinical studies have shown that the combination is well-tolerated and may provide enhanced efficacy compared to either agent alone, particularly in cancers such as squamous cell carcinoma of the head and neck (SCCHN) and docetaxel-resistant prostate cancer[1][2]. The rationale for combining these agents lies in their complementary mechanisms—celecoxib reduces prostaglandin synthesis involved in tumorigenesis, while gefitinib blocks EGFR signaling critical for cancer cell growth.

02

Targets

PTGS2 (Prostaglandin-Endoperoxide Synthase 2)EGFR (Epidermal growth factor receptor)

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