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Furmonertinib Mesilate Tablets

Allist Pharmaceuticals, Inc. · Phase 3 active Small molecule

Furmonertinib is a third-generation EGFR tyrosine kinase inhibitor that irreversibly binds to and inhibits mutant EGFR, including T790M resistance mutations.

Furmonertinib is a third-generation EGFR tyrosine kinase inhibitor that irreversibly binds to and inhibits mutant EGFR, including T790M resistance mutations. Used for Non-small cell lung cancer with EGFR mutations, including T790M resistance mutations.

At a glance

Generic nameFurmonertinib Mesilate Tablets
Also known asAST2818
SponsorAllist Pharmaceuticals, Inc.
Drug classThird-generation EGFR tyrosine kinase inhibitor
TargetEGFR (epidermal growth factor receptor)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Furmonertinib selectively targets epidermal growth factor receptor (EGFR) mutations commonly found in non-small cell lung cancer, particularly overcoming resistance mechanisms like the T790M mutation that render first and second-generation EGFR inhibitors ineffective. By irreversibly binding to the ATP-binding pocket of mutant EGFR, it suppresses downstream signaling pathways that drive cancer cell proliferation and survival.

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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