Futuximab

drug
On this page

Also known as 992 DSSYM-004Sym004

Summary

Futuximab (CHEMBL2109388) is a phase-3 clinical-stage antibody; indicated across 4 conditions including squamous cell carcinoma and glioma.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 4 conditions
  • Clinical trials: 10

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2109388
NameFutuximab
TypeAntibody
Max phase3

Also known as: 992 DS, Futuximab, SYM-004, Sym004, FUTUXIMAB

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

4 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
squamous cell carcinoma2MONDO:0005096EFO:0000707
glioma2MONDO:0021042MONDO:0100342
neoplasm1MONDO:0005070EFO:0000616
non-small cell lung carcinoma1MONDO:0005233EFO:0003060

Clinical trials

Total trials: 10.

Phase distribution

PhaseTrials
PHASE24
PHASE1/PHASE23
PHASE32
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03717038PHASE3WITHDRAWNSym004 Versus TAS-102 in Patients With mCRC
NCT05223673PHASE3TERMINATEDPhase 3 Study of Futuximab/Modotuximab in Combination With Trifluridine/Tipiracil Versus Trifluridine/Tipiracil Single Agent in Participants With Previously Treated Metastatic Colorectal Cancer
NCT01117428PHASE1/PHASE2COMPLETEDSym004 in Patients With Advanced Solid Tumors
NCT01417936PHASE2COMPLETEDSym004 in SCCHN Patients Failing Anti-EGFR Based Therapy
NCT02083653PHASE2COMPLETEDSym004 vs Standard of Care in Subjects With Metastatic Colorectal Cancer
NCT02568046PHASE1/PHASE2TERMINATEDSym004 in Combination With FOLFIRI in Metastatic Colorectal Cancer Patients
NCT02924233PHASE1/PHASE2WITHDRAWNSym004 in Combination With Nivolumab Versus Nivolumab Monotherapy in EGFR-amplified Squamous Non-Small Cell Lung Cancer
NCT02965417PHASE2WITHDRAWNSym004 in Metastatic Colorectal Cancer and ECD-EGFR Patients
NCT03549338PHASE2TERMINATEDSym004 Versus Futuximab or Modotuximab in Patients With mCRC
NCT01955473PHASE1COMPLETEDJapanese Phase 1 Trial of Sym004 in Solid Tumors

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).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.