Antimony

drug
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Also known as Antimony blackAntimony elementelementalC.I. 77050Metallic antimonyPrepared metallic antimonySBStibium metallicum

Summary

Antimony (CHEMBL4297652) is a phase-3 clinical-stage small molecule; indicated across 2 conditions including peripheral neuropathy and cutaneous leishmaniasis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 2 conditions
  • Clinical trials: 3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4297652
NameAntimony
TypeSmall molecule
Max phase3

Also known as: Antimony, Antimony black, Antimony element, elemental, C.I. 77050, Metallic antimony, Prepared metallic antimony, SB, Stibium metallicum, ANTIMONY

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

2 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
peripheral neuropathy3MONDO:0005244EFO:0003100
cutaneous leishmaniasis2MONDO:0005446EFO:0005046

Clinical trials

Total trials: 3.

Phase distribution

PhaseTrials
PHASE22
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00233545PHASE2COMPLETEDMiltefosine to Treat Cutaneous Leishmaniasis in Bolivia
NCT01380301PHASE2TERMINATEDTreatment of Cutaneous Leishmaniasis With a Combination of Miltefosine and Antimony
NCT00469495Not specifiedCOMPLETEDAntihelminthic Therapy Combined With Antimony in the Treatment of Cutaneous Leishmaniasis

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).