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Patritumab deruxtecan (HER3-DXd)

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDDRUG-PATRITUMAB-DERUXTECAN
TypeDrug
Aliases
Патритумаб дерукстекан
Statuspending_clinical_signoff
DiseasesDIS-NSCLC
SourcesSRC-ESMO-NSCLC-METASTATIC-2024 SRC-NCCN-NSCLC-2025

Drug Facts

ClassHER3-targeted antibody-drug conjugate (deruxtecan / topo-I inhibitor payload)
MechanismFully human anti-HER3 (ERBB3) IgG1 monoclonal antibody linked to deruxtecan (DXd, exatecan-derivative topoisomerase-I inhibitor) via cleavable tetrapeptide linker. Drug-to-antibody ratio ~8:1 with bystander effect. HER3 is broadly expressed across solid tumors and frequently upregulated as a resistance mechanism after EGFR TKI in EGFR-mutant NSCLC.
Typical dosing5.6 mg/kg IV q3 weeks until disease progression or unacceptable toxicity (HERTHENA-Lung01 schedule). Premedicate with antiemetics; high-emetogenicity prophylaxis recommended.
Ukraine registeredFalse
NSZU reimbursedFalse
Ukraine last verified2026-04-29

Notes

HERTHENA-Lung01 (NCT04619004): Phase II, EGFR-mutated metastatic NSCLC after EGFR TKI + platinum-based chemo. ORR 29.8%, mPFS 5.5 mo, mOS 11.9 mo. Filed for FDA accelerated approval Dec 2023; CRL received Jun 2024 (third-party manufacturing issue, not efficacy/safety). Distinct AE profile vs other DXd ADCs: cytopenias more prominent than ILD. Status as of 2026-04: investigational only; not commercially available. Trial-source SRC for HERTHENA-Lung01 not yet ingested into KB — FLAG for follow-up.

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