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HMPL-760

Hutchmed · Phase 3 active Small molecule

HMPL-760 is a selective inhibitor of fibroblast growth factor receptor (FGFR) that blocks aberrant FGFR signaling in cancer cells.

HMPL-760 is a selective inhibitor of fibroblast growth factor receptor (FGFR) that blocks aberrant FGFR signaling in cancer cells. Used for Cholangiocarcinoma with FGFR2 fusion or rearrangement, Urothelial carcinoma with FGFR alterations, Other solid tumors with FGFR genetic alterations.

At a glance

Generic nameHMPL-760
SponsorHutchmed
Drug classFGFR inhibitor
TargetFGFR (Fibroblast Growth Factor Receptor)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

HMPL-760 selectively targets FGFR kinases, which are frequently dysregulated in various solid tumors through mutations, amplifications, or translocations. By inhibiting FGFR-mediated signaling pathways, the drug suppresses tumor cell proliferation and survival in FGFR-dependent cancers. This mechanism is particularly relevant in tumors with FGFR alterations where the pathway drives oncogenic growth.

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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