Nifurtimox

drug
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Also known as BAY 2502BAY A2502BAY-2502BAY-A2502BAYER 2502BAYER-2502DNDI1613515LampitNifurtimoxumMMV001499NifrutimoxC0237391

Summary

Nifurtimox (CHEMBL290960) is an approved small molecule (ATC P01CC01); indicated across 6 conditions including trypanosomiasis and chagas disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: P01CC01
  • Indications: 6 conditions
  • Clinical trials: 9
  • Chemistry: 287.29 Da · C10H13N3O5S

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL290960
NameNifurtimox
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID6842999
ATCP01CC01
Molecular formulaC10H13N3O5S
Molecular weight287.29
InChIKeyARFHIAQFJWUCFH-IZZDOVSWSA-N

SMILES: CC1CS(=O)(=O)CCN1/N=C/C2=CC=C(O2)[N+](=O)[O-]

IUPAC name: (E)-N-(3-methyl-1,1-dioxo-1,4-thiazinan-4-yl)-1-(5-nitrofuran-2-yl)methanimine

Also known as: BAY 2502, BAY A2502, BAY-2502, BAY-A2502, BAYER 2502, BAYER-2502, DNDI1613515, Lampit, Nifurtimox, Nifurtimoxum, nifurtimox, NIFURTIMOX

Patent coverage: 25 distinct patent families (37 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

6 indications (4 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
trypanosomiasis4MONDO:0000940DOID:10113
Chagas disease4MONDO:0001444EFO:0008559
leishmaniasis4MONDO:0011989EFO:0005044
human African trypanosomiasis2MONDO:0005459EFO:0005225
neuroblastoma1MONDO:0005072EFO:0000621

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 9.

Phase distribution

PhaseTrials
PHASE32
PHASE2/PHASE32
PHASE22
PHASE12
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00146627PHASE3COMPLETEDEfficacy - Safety of Eflornithine-Nifurtimox Combination Versus Eflornithine to Treat Human African Trypanosomiasis
NCT00330148PHASE3TERMINATEDRandomized Clinical Trial of Three Drug Combinations for Late-Stage Gambiense Human African Trypanosomiasis
NCT01685827PHASE2/PHASE3COMPLETEDPivotal Study of Fexinidazole for Human African Trypanosomiasis in Stage 2
NCT02369978PHASE2/PHASE3UNKNOWNCHICAMOCHA 3 - Equivalence of Usual Interventions for Trypanosomiasis (EQUITY)
NCT00601003PHASE2COMPLETEDStudy of Nifurtimox to Treat Refractory or Relapsed Neuroblastoma or Medulloblastoma
NCT03981523PHASE2COMPLETEDNew Therapies and Biomarkers for Chagas Infection
NCT00486564PHASE1COMPLETEDSafety Study of Nifurtimox for Relapsed or Refractory Neuroblastoma
NCT02606864PHASE1COMPLETEDStudy to Assess the Food Effect on the Pharmacokinetics of Nifurtimox Tablets in Chronic Chagas’ Patients
NCT05477953Not specifiedNOT_YET_RECRUITINGAn Observational Pregnancy Safety Study in Women Who Were Exposed to the Drug Nifurtimox During Pregnancy to Learn About the Risk of Pregnancy Complications and About the Mother’s and Baby’s Health

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

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