Human Coagulation Factor Viii

drug
On this page

Also known as Antihemophilic factorAntihemophilic factor (human)Antihemophilic factor humanAntihemophilic factor viii humanhumanAntihemophilic human plasmaFactor viii (antihaemophilic factor)Factor viii (human)Factor viiiFactorateHemofil mMonoclate-p

Summary

Human Coagulation Factor Viii (CHEMBL2108175) is an approved unknown; indicated across 4 conditions including von willebrand disease (hereditary or acquired) and hemophilia a.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Unknown
  • Indications: 4 conditions
  • Clinical trials: 7

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108175
NameHuman Coagulation Factor Viii
TypeUnknown
Max phase4

Also known as: Antihemophilic factor, Antihemophilic factor (human), Antihemophilic factor human, Antihemophilic factor viii human, human, Antihemophilic human plasma, Factor viii (antihaemophilic factor), Factor viii (human), Factor viii, Factorate, Hemofil m, Human coagulation factor viii

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 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
von Willebrand disease (hereditary or acquired)4MONDO:0024574Orphanet:903
hemophilia A4MONDO:0010602MONDO:0010602

2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 7.

Phase distribution

PhaseTrials
PHASE2/PHASE33
PHASE42
PHASE31
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00243386PHASE4COMPLETEDProphylaxis Study of Recombinant Factor VIII Manufactured Protein-Free (rAHF-PFM) in Patients With Hemophilia A
NCT00289536PHASE4COMPLETEDDose-Response Study of Recombinant Factor VIII Manufactured Protein-Free (rAHF-PFM) in Patients With Hemophilia A
NCT07416526PHASE3RECRUITINGA Clinical Study to Evaluate the Effects of NXT007 Compared to Factor VIII Prophylaxis in Participants With Hemophilia A
NCT00157040PHASE2/PHASE3COMPLETEDStudy of Pharmacokinetics, Efficacy, and Safety of a Recombinant and Protein-Free Factor VIII (rAHF-PFM) in Pediatric Patients With Hemophilia A
NCT00157053PHASE2/PHASE3COMPLETEDStudy of Pharmacokinetics, Efficacy and Safety of a Recombinant and Protein-Free Factor VIII (rAHF-PFM) in Hemophilia A Patients - A Continuation of Clinical Study 069901
NCT00157105PHASE2/PHASE3COMPLETEDSafety and Efficacy Study of a Recombinant and Protein-Free Factor VIII (rAHF-PFM) in Hemophilia A Patients Undergoing Surgery
NCT00952822PHASE1COMPLETEDPharmacokinetic Study of ADVATE Reconstituted in 2 mL Sterile Water for Injection

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).