AUTOLOGOUS PERIPHERAL-BLOOD MONONUCLEAR CELLS INCLUDING A MINIMUM OF 50 MILLION AUTOLOGOUS CD54+ CELLS ACTIVATED WITH PROSTATIC ACID PHOSPHATASE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR

drug
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Also known as Provenge

Summary

Autologous Peripheral-Blood Mononuclear Cells Including A Minimum Of 50 Million Autologous Cd54+ Cells Activated With Prostatic Acid Phosphatase Granulocyte-Macrophage Colony-Stimulating Factor (CHEMBL5315067) is an approved unknown; indicated across 2 conditions including prostate cancer and prostate carcinoma.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Unknown
  • Indications: 2 conditions
  • Clinical trials: 1

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL5315067
NameAUTOLOGOUS PERIPHERAL-BLOOD MONONUCLEAR CELLS INCLUDING A MINIMUM OF 50 MILLION AUTOLOGOUS CD54+ CELLS ACTIVATED WITH PROSTATIC ACID PHOSPHATASE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR
TypeUnknown
Max phase4

Also known as: Provenge

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 (2 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
prostate cancer4MONDO:0008315MONDO:0008315
prostate carcinoma4MONDO:0005159EFO:0001663

Clinical trials

Total trials: 1.

Phase distribution

PhaseTrials
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02232230Not specifiedCOMPLETEDA Multicenter Trial Enrolling Men With Advanced Prostate Cancer Who Are to Receive Combination Radiation and Sipuleucel-T

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).