Lipegfilgrastim

drug
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Also known as LonquexXM-22XM22

Summary

Lipegfilgrastim (CHEMBL4594230) is an approved protein (ATC L03AA14); indicated across 4 conditions including neoplasm and neutropenia.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Protein
  • ATC class: L03AA14
  • Indications: 4 conditions
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4594230
NameLipegfilgrastim
TypeProtein
Max phase4
ATCL03AA14

Also known as: Lipegfilgrastim, Lonquex, XM-22, XM22, LIPEGFILGRASTIM

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
neoplasm4MONDO:0005070EFO:0000616
neutropenia4MONDO:0001475MONDO:0001475

2 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
lymphoma3MONDO:0005062EFO:0000574
Ewing sarcoma1MONDO:0012817EFO:0000174

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE12
PHASE31
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02044276PHASE3COMPLETEDA comparatiVe Study on Efficacy and Safety of Lipegfilgrastim in Comparison to Pegfilgrastim in Elderly Patients With Aggressive B Cell Non-HOdgkin Lymphomas at hIgh Risk for R-CHOP-21-inDuced Neutropenia
NCT01585649PHASE1COMPLETEDPK/PD of XM22 in Children With Ewing Family of Tumors or Rhabdomyosarcoma
NCT02306915PHASE1COMPLETEDPK, PD, Safety and Tolerability of Lipegfilgrastim in Healthy Japanese and Caucasian Participants
NCT02527317Not specifiedCOMPLETEDDose Dense Chemotherapy With Lipegfilgrastim Support in Early Breast Cancer

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).