Laromustine

drug
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Also known as 101MCloretazineLaromustinLaromustinaNSC-734246OnriginVNP-40101MVNP40101M

Summary

Laromustine (CHEMBL167691) is a phase-3 clinical-stage small molecule; indicated across 7 conditions including leukemia and lung neoplasm.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 7 conditions
  • Clinical trials: 15
  • Chemistry: 307.8 Da · C6H14ClN3O5S2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL167691
NameLaromustine
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID3081349
Molecular formulaC6H14ClN3O5S2
Molecular weight307.8
InChIKeyPVCULFYROUOVGJ-UHFFFAOYSA-N

SMILES: CNC(=O)N(N(CCCl)S(=O)(=O)C)S(=O)(=O)C

IUPAC name: 1-[2-chloroethyl(methylsulfonyl)amino]-3-methyl-1-methylsulfonylurea

Also known as: 101M, Cloretazine, Laromustin, Laromustina, Laromustine, NSC-734246, Onrigin, VNP-40101M, VNP40101M, LAROMUSTINE

Patent coverage: 154 distinct patent families (370 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

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

7 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
leukemia3MONDO:0005059EFO:0000565
lung neoplasm2MONDO:0021117MONDO:0008903
myelodysplastic syndrome1MONDO:0018881EFO:0000198
acute myeloid leukemia1MONDO:0018874EFO:0000222
lymphoma1MONDO:0005062EFO:0000574
central nervous system neoplasm1MONDO:0006130EFO:1000158
neoplasm1MONDO:0005070MONDO:0004992

Clinical trials

Total trials: 15.

Phase distribution

PhaseTrials
PHASE18
PHASE23
PHASE1/PHASE23
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00112554PHASE3COMPLETEDCytarabine With or Without VNP40101M in Treating Patients With Relapsed Acute Myeloid Leukemia
NCT00083187PHASE2COMPLETEDVNP40101M in Treating Patients With Acute Myelogenous Leukemia or High-Risk Myelodysplasia
NCT00282022PHASE2COMPLETEDVNP40101M in Treating Patients With Relapsed or Refractory Locally Advanced or Metastatic Small Cell Lung Cancer
NCT00304005PHASE1/PHASE2COMPLETEDVNP40101M in Treating Patients With Richter Syndrome or Refractory or Relapsed Chronic Lymphocytic Leukemia or Other Lymphoproliferative Disorders
NCT00354276PHASE2UNKNOWNVNP40101M Followed by Cytarabine in Treating Older Patients With Acute Myeloid Leukemia
NCT00655395PHASE1/PHASE2TERMINATEDTreatment of Elderly Patients With Acute Myeloid Leukemia (AML) and High Risk Myelodysplastic (MD) Syndrome With Laromustine and Infusional Cytarabine
NCT00840684PHASE1/PHASE2COMPLETEDLaromustine, Daunorubicin, and Cytarabine in Treating Patients With Acute Myeloid Leukemia
NCT00025129PHASE1COMPLETEDVNP40101M in Treating Patients With Advanced Solid Tumors or Lymphomas
NCT00049686PHASE1COMPLETEDVNP40101M in Treating Patients With Relapsed or Refractory Leukemia or Myelodysplastic Syndrome
NCT00049699PHASE1COMPLETEDVNP40101M in Treating Patients With Advanced or Metastatic Cancer
NCT00070538PHASE1COMPLETEDVNP40101M and Cytarabine in Treating Patients With Hematologic Malignancies
NCT00098436PHASE1COMPLETEDTemozolomide and VNP40101M in Treating Patients With Relapsed or Refractory Leukemias
NCT00098761PHASE1COMPLETEDVNP40101M in Treating Young Patients With Recurrent, Progressive, or Refractory Primary Brain Tumors
NCT00516282PHASE1TERMINATEDVNP40101M and Temozolomide in Treating Patients With Progressive or Relapsed Malignant Glioma
NCT00521859PHASE1COMPLETEDCloretazine (VNP40101M) With Hematopoietic Cell Transplantation for Hematologic Malignancies

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).