Dociparstat Sodium

drug
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Also known as Dociparstat sodicoDociparstat sodiqueGM-1892ODSH

Summary

Dociparstat Sodium (CHEMBL3990006) is a phase-3 clinical-stage unknown; indicated across 2 conditions including acute myeloid leukemia and exocrine pancreatic carcinoma.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • Indications: 2 conditions
  • Clinical trials: 6

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3990006
NameDociparstat Sodium
TypeUnknown
Max phase3

Also known as: Dociparstat sodico, Dociparstat sodique, Dociparstat sodium, GM-1892, ODSH, DOCIPARSTAT 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
acute myeloid leukemia3MONDO:0018874EFO:0000222
exocrine pancreatic carcinoma2MONDO:0005192EFO:0002618

Clinical trials

Total trials: 6.

Phase distribution

PhaseTrials
PHASE22
PHASE12
PHASE2/PHASE31
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04389840PHASE2/PHASE3TERMINATEDDociparstat for the Treatment of Severe COVID-19 in Adults at High Risk of Respiratory Failure
NCT00457951PHASE2TERMINATEDA Study Designed to Evaluate ODSH in Subjects With Exacerbations of COPD
NCT02873338PHASE2COMPLETEDDociparstat Sodium (CX-01) Combined With Standard Induction Therapy for Newly Diagnosed Acute Myeloid Leukemia
NCT02056782PHASE1COMPLETEDA Pilot Study of Dociparstat Sodium (ODSH) in Acute Myeloid Leukemia
NCT02164097PHASE1TERMINATEDODSH + ICE Chemotherapy in Pediatric Solid Tumors
NCT01843634EARLY_PHASE1COMPLETEDPh I Safety and Efficacy of ODSH in Patients Receiving Induction or Consolidation Therapy for Acute Myeloid Leukemia

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).