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Erlotinib, Pemetrexed

Hunan Province Tumor Hospital · FDA-approved active Small molecule

This combination uses erlotinib to inhibit EGFR signaling and pemetrexed to disrupt folate-dependent nucleotide synthesis, together targeting non-small cell lung cancer through dual pathways.

This combination uses erlotinib to inhibit EGFR signaling and pemetrexed to disrupt folate-dependent nucleotide synthesis, together targeting non-small cell lung cancer through dual pathways. Used for Non-small cell lung cancer (NSCLC), likely EGFR-mutant or advanced disease.

At a glance

Generic nameErlotinib, Pemetrexed
SponsorHunan Province Tumor Hospital
Drug classEGFR tyrosine kinase inhibitor + antifolate antimetabolite
TargetEGFR; thymidylate synthase and folate-dependent enzymes
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Erlotinib is a small-molecule tyrosine kinase inhibitor that blocks epidermal growth factor receptor (EGFR) signaling, preventing tumor cell proliferation in EGFR-mutant or EGFR-dependent cancers. Pemetrexed is an antifolate antimetabolite that inhibits thymidylate synthase and other folate-dependent enzymes, disrupting DNA and RNA synthesis. The combination leverages complementary mechanisms to enhance cytotoxic and targeted effects in lung cancer.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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