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Anlotinib plus Pemetrexed

Henan Provincial People's Hospital · FDA-approved active Small molecule

Anlotinib inhibits multiple receptor tyrosine kinases to block tumor angiogenesis, while pemetrexed inhibits folate-dependent enzymes to disrupt DNA synthesis in cancer cells.

Anlotinib inhibits multiple receptor tyrosine kinases to block tumor angiogenesis, while pemetrexed inhibits folate-dependent enzymes to disrupt DNA synthesis in cancer cells. Used for Non-small cell lung cancer (NSCLC), likely advanced or metastatic stages.

At a glance

Generic nameAnlotinib plus Pemetrexed
SponsorHenan Provincial People's Hospital
Drug classMulti-target tyrosine kinase inhibitor plus antifolate antimetabolite
TargetVEGFR, FGFR, RET, c-Kit (anlotinib); thymidylate synthase, DHFR, GARFT (pemetrexed)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Anlotinib is a multi-target tyrosine kinase inhibitor that suppresses VEGFR, FGFR, and other kinases involved in tumor blood vessel formation and growth. Pemetrexed is an antifolate agent that inhibits thymidylate synthase and other folate-dependent enzymes, disrupting nucleotide synthesis and inducing apoptosis. The combination leverages complementary mechanisms: antiangiogenic activity plus direct cytotoxic chemotherapy.

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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