Semuloparin Sodium

drug
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Also known as AVE-5026MulsevoSemuloparina sodicaSemuloparine sodiqueVisamerin

Summary

Semuloparin Sodium (CHEMBL2108718) is a phase-3 clinical-stage oligosaccharide; indicated across 2 conditions including venous thromboembolism.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Oligosaccharide
  • Indications: 2 conditions
  • Clinical trials: 9

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108718
NameSemuloparin Sodium
TypeOligosaccharide
Max phase3

Also known as: AVE-5026, Mulsevo, Semuloparin sodium, Semuloparina sodica, Semuloparine sodique, Visamerin, SEMULOPARIN SODIUM

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
venous thromboembolism3MONDO:0005399EFO:0004286

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
PHASE37
PHASE22

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00679588PHASE3COMPLETEDEvaluation of AVE5026 as Compared to Enoxaparin for the Prevention of Venous Thromboembolism in Patients Undergoing Major Abdominal Surgery
NCT00694382PHASE3COMPLETEDEvaluation of AVE5026 in the Prevention of Venous Thromboembolism in Cancer Patients Undergoing Chemotherapy
NCT00697099PHASE3COMPLETEDEvaluation of AVE5026 as Compared to Enoxaparin for the Prevention of Thromboembolism in Patients Undergoing Total Hip Replacement Surgery
NCT00709904PHASE3COMPLETEDEvaluation of AVE5026 as Compared to Placebo for the Extended Prophylaxis of Venous Thromboembolism in Patients Having Undergone Hip Fracture Surgery
NCT00714597PHASE3TERMINATEDEvaluation of AVE5026 in the Prevention of Venous Thromboembolism in Acutely Ill Medical Patients With Restricted Mobility
NCT00718224PHASE3COMPLETEDEvaluation of AVE5026 as Compared to Enoxaparin for the Prevention of Thromboembolism in Patients Undergoing Elective Knee Replacement Surgery
NCT00721760PHASE3COMPLETEDEvaluation of AVE5026 as Compared to Enoxaparin for the Prevention of Thromboembolism in Patients Undergoing Hip Fracture Surgery
NCT00331838PHASE2COMPLETEDPrevention of Venous Thromboembolism in Patients Undergoing Elective Total Knee Replacement Surgery
NCT01567904PHASE2TERMINATEDStudy of AVE5026 at Weight-adjusted Doses in Children With a Central Venous Line

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).