Platelet Concentrate

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Summary

Platelet Concentrate (CHEMBL2108774) is a phase-3 clinical-stage unknown; indicated across 3 conditions including autoimmune thrombocytopenic purpura and hematopoietic and lymphoid system neoplasm.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • Indications: 3 conditions
  • Clinical trials: 4

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2108774
NamePlatelet Concentrate
TypeUnknown
Max phase3

Also known as: Platelet concentrate, PLATELET CONCENTRATE

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 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
autoimmune thrombocytopenic purpura3MONDO:0008558EFO:0007160
hematopoietic and lymphoid system neoplasm2MONDO:0002334MONDO:0044881

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

Clinical trials

Total trials: 4.

Phase distribution

PhaseTrials
PHASE42
PHASE31
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05667805PHASE4RECRUITINGCoagulation in Cirrhosis
NCT01955811PHASE4COMPLETEDStudy to Reveal if Fibrinogen Treatment Effects Blood Clotting Better Than a Platelet Transfusion
NCT03492515PHASE3UNKNOWNRecombinant Human Thrombopoietin(rhTPO) in Pregnancy With Immune Thrombocytopenia
NCT03196310Not specifiedTERMINATEDSingle Blinded First CMC Osteoarthritis Treatment

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).