Meglumine Antimonate

drug
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Also known as GlucantimGlucantimeMeglumine antimoniateN-methylglucamine antimonateN-methylglucamine antimoniateglucatimN-methylglucomine antimoniateANTIMONIATE_DE_MEGLUMINEglucantime stibenic acidMeglumine Antimoniate

Summary

Meglumine Antimonate (CHEMBL239129) is a phase-3 clinical-stage small molecule (ATC P01CB01); indicated across 5 conditions including cutaneous leishmaniasis and leishmaniasis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: P01CB01
  • Indications: 5 conditions
  • Clinical trials: 18

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL239129
NameMeglumine Antimonate
TypeSmall molecule
Max phase3
ATCP01CB01

Also known as: Glucantim, Glucantime, Meglumine antimonate, Meglumine antimoniate, N-methylglucamine antimonate, meglumine antimoniate, glucantime, N-methylglucamine antimoniate, glucatim, N-methylglucomine antimoniate, ANTIMONIATE_DE_MEGLUMINE, glucantime stibenic acid

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

5 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
cutaneous leishmaniasis3MONDO:0005446EFO:0005046
leishmaniasis3MONDO:0011989EFO:0005044
trypanosomiasis3MONDO:0000940DOID:10113
bipolar disorder3MONDO:0004985MONDO:0004985
mucocutaneous leishmaniasis2MONDO:0005859EFO:0007379

Clinical trials

Total trials: 18.

Phase distribution

PhaseTrials
PHASE26
PHASE35
PHASE43
PHASE2/PHASE33
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00317980PHASE4COMPLETEDSafety and Efficacy of Low-Dose Pentavalent Antimony for Treatment of Cutaneous Leishmaniasis
NCT00818818PHASE4COMPLETEDLow-dose Pentavalent Antimony Treatment of Cutaneous Leishmaniasis in Old Age Patients
NCT01032187PHASE4COMPLETEDAmphotericin B to Treat Visceral Leishmaniasis in Brazilian Children
NCT00317629PHASE3TERMINATEDControlled Nitric Oxide Releasing Patch Versus Meglumine Antimoniate in the Treatment of Cutaneous Leishmaniasis
NCT00487253PHASE3UNKNOWNOral Miltefosine for the Treatment of Pediatric Cutaneous Leishmaniasis in Colombia
NCT01301924PHASE2/PHASE3COMPLETEDComparison of Standard and Alternative Antimonial Dosage in Patients With American Cutaneous Leishmaniasis
NCT01301937PHASE2/PHASE3UNKNOWNLow Antimonial Dosage in American Mucosal Leishmaniasis
NCT01464242PHASE2/PHASE3COMPLETEDAdd-on Study of Pentoxifylline in Cutaneous Leishmaniasis
NCT01953744PHASE3TERMINATEDHigh Dose Fluconazole in Cutaneous Leishmaniasis in Bahia and Manaus
NCT04340128PHASE3COMPLETEDEfficacy of Intra-lesional Injections of Glucantime Once a Week or Twice a Week in the Treatment of Anthroponotic Cutaneous Leishmaniasis (ACL)
NCT04515186PHASE3COMPLETEDCombination, Miltefosine Monotherapy for Cutaneous Leishmaniasis in New World
NCT02530697PHASE2ACTIVE_NOT_RECRUITINGThe Association of Miltefosine and Pentoxifylline to Treat Mucosal and Cutaneous Leishmaniasis: A Clinical Trial in Brazil
NCT00004755PHASE2COMPLETEDAllopurinol, Glucantime, or Allopurinol/Glucantime for Cutaneous Leishmaniasis in Brazil
NCT00537953PHASE2UNKNOWNShort Course of Miltefosine and Antimony to Treat Cutaneous Leishmaniasis in Bolivia
NCT00973128PHASE2COMPLETEDReduced Doses of Antimony Plus Ranulocyte Monocyte Colony Stimulating Factor (GM-CSF) for Cutaneous Leishmaniasis
NCT03084952PHASE2UNKNOWNPhase 2 Trial to Evaluate 18-Methoxycoronaridine Efficacy, Safety and Tolerability in Cutaneous Leishmaniasis Patients
NCT03294161PHASE2COMPLETEDFourth-generation Immucillin Derivative DI4G Associated Therapy in Cutaneous Leishmaniasis
NCT00480883Not specifiedCOMPLETEDTreatment of Cutaneous Leishmaniasis With Meglumine Antimoniate Versus Meglumine Antimoniate and Allopurinol

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).