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Avelumab

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

IDDRUG-AVELUMAB
TypeDrug
Aliases
BavencioАвелумаб
Statusreviewed 2026-04-27 | pending_clinical_signoff
DiseasesDIS-NK-T-NASAL DIS-UROTHELIAL
SourcesSRC-NCCN-BCELL-2025 SRC-NCCN-NSCLC-2025

Drug Facts

ClassAnti-PD-L1 monoclonal antibody (IgG1 with preserved ADCC)
MechanismFully human IgG1 anti-PD-L1 antibody. Blocks PD-L1 binding to PD-1 and CD80, restoring T-cell antitumor immunity. The IgG1 isotype retains antibody-dependent cellular cytotoxicity (ADCC) — distinct from IgG4 anti-PD-L1 agents — relevant for NK-cell engagement in certain tumor types.
Typical dosing800 mg IV every 2 weeks (or 10 mg/kg q2w in older labeling). Premedication for first 4 infusions (paracetamol + diphenhydramine).
Ukraine registeredFalse
NSZU reimbursedFalse
Ukraine last verified2026-04-27

Notes

Multi-indication anti-PD-L1: FDA-approved for metastatic Merkel cell carcinoma (JAVELIN Merkel 200), urothelial maintenance after platinum (JAVELIN Bladder 100), and 1L RCC + axitinib (JAVELIN Renal 101). In NK/T-cell lymphoma: phase 2 data (Kim 2020 Blood) showed ORR ~38% in r/r EBV-driven NK/T-NL exploiting EBV/PD-L1 signaling axis. Off-label for hematologic indications. Standard ICI immune- mediated AE management protocol applies (steroid taper, treatment hold thresholds per NCCN immunotherapy toxicity guidelines).

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