Ancrod

drug
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Also known as Acc-cArvinArwinEc 3.4.21.74Protein c activatorProteinaseagkistrodon serineVenombin-aViprinex

Summary

Ancrod (CHEMBL2108481) is a phase-3 clinical-stage unknown (ATC B01AD09); indicated across 1 condition including thrombotic disease.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • ATC class: B01AD09
  • Indications: 1 condition
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108481
NameAncrod
TypeUnknown
Max phase3
ATCB01AD09

Also known as: Acc-c, Ancrod, Arvin, Arwin, Ec 3.4.21.74, Protein c activator, Proteinase, agkistrodon serine, Venombin-a, Viprinex, ANCROD

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
thrombotic disease3MONDO:0000831HP:0004419

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE33
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00141011PHASE3TERMINATEDAncrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke
NCT00300196PHASE3TERMINATEDASP-II: Ancrod Stroke Program: Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke
NCT00343174PHASE3COMPLETEDIntravenous Ancrod for the Treatment of Acute Ischemic Stroke Within 6 Hours After Onset of Symptoms
NCT01621256PHASE1/PHASE2COMPLETEDEfficacy, Safety, and Tolerability of Ancrod in Patients With Sudden Hearing Loss

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).