Samarium

drug
On this page

Also known as SM

Summary

Samarium (CHEMBL4300244) is a phase-3 clinical-stage small molecule; indicated across 1 condition including metastatic prostate carcinoma.

At a glance

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

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4300244
NameSamarium
TypeSmall molecule
Max phase3

Also known as: Samarium, SM, SAMARIUM

Parent form; salt/anhydrous children: CHEMBL4297426

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
metastatic prostate carcinoma2MONDO:0004956EFO:0000196

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE1/PHASE22
PHASE22

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00121095PHASE1/PHASE2UNKNOWNStudy of Samarium Sm-153 Lexidronam Combined With Docetaxel for Patients With Prostate Cancer
NCT00126230PHASE2TERMINATEDTrial of Docetaxel-Samarium in Patients With Hormone-Refractory Advanced Prostate Cancer
NCT00374751PHASE1/PHASE2COMPLETEDEffect of Samarium on the Relief of Pain Due to Vertebral Metastases
NCT00551525PHASE2COMPLETEDSamarium Sm 153 Lexidronam Pentasodium and 3-Dimensional Conformal Radiation Therapy or Intensity-Modulated Radiation Therapy in Treating Patients With Rising Prostate-Specific Antigen Levels After Radical Prostatectomy for Prostate Cancer

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).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.