Gemtuzumab

drug
On this page

Also known as Gemtuzumab component of mylotargHp 67.6

Summary

Gemtuzumab (CHEMBL2108342) is a phase-3 clinical-stage antibody; indicated across 1 condition including acute myeloid leukemia.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Antibody
  • Indications: 1 condition
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108342
NameGemtuzumab
TypeAntibody
Max phase3

Also known as: Gemtuzumab, Gemtuzumab component of mylotarg, Hp 67.6, GEMTUZUMAB

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

1 indication (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
acute myeloid leukemia3MONDO:0018874EFO:0000222

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE32
PHASE41
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01041040PHASE4COMPLETEDLAM07: Study to Analyze the Efficacy of a Risk Adapted Treatment Strategy, Including Gemtuzumab Ozogamicin (GO) During Consolidation, for Patients With Acute Myeloid Leukemia (AML)
NCT00136084PHASE3COMPLETEDTreatment of Patients With Newly Diagnosed Acute Myeloid Leukemia or Myelodysplasia
NCT00860639PHASE3COMPLETEDEfficacy of Gemtuzumab Ozogamycin for Patients Presenting an Acute Myeloid Leukemia (AML) With Intermediate Risk
NCT06448013PHASE1RECRUITINGA Phase I Study Investigating the Combination of the Menin Inhibitor Ziftomenib With Venetoclax and Gemtuzumab in Pediatric Patients With Acute Myeloid Leukemia

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).