Tinzaparin

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Summary

Tinzaparin (CHEMBL6068592) is a phase-3 clinical-stage oligosaccharide targeting SERPINC1; indicated across 3 conditions including colorectal adenocarcinoma and plasma cell myeloma.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Oligosaccharide
  • Targets: 1 (SERPINC1)
  • Indications: 3 conditions
  • Clinical trials: 29

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL6068592
NameTinzaparin
TypeOligosaccharide
Max phase3

Also known as: Tinzaparin, TINZAPARIN

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
SERPINC1serpin family C member 1Activation0%P01008

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): SERPINC1.

Top Reactome pathways

12 total, by targets touching each:

PathwayTargetsGenes
Hemostasis1SERPINC1
R-HSA-1408371SERPINC1
R-HSA-1408751SERPINC1
R-HSA-1408771SERPINC1
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)1SERPINC1
Metabolism of proteins1SERPINC1
Post-translational protein modification1SERPINC1
Post-translational protein phosphorylation1SERPINC1
Fibrin formation1SERPINC1
Initiation of coagulation cascade1SERPINC1
Regulation of clotting cascade1SERPINC1
Amplification and propagation of coagulation cascade1SERPINC1

Dominant GO biological processes

GO termTargets
blood coagulation1
regulation of blood coagulation1
hemostasis1

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
colorectal adenocarcinoma3MONDO:0005008EFO:0000365
plasma cell myeloma2MONDO:0009693EFO:0001378

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

Clinical trials

Total trials: 29.

Phase distribution

PhaseTrials
PHASE411
Not specified10
PHASE35
PHASE22
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05245877PHASE4RECRUITINGPre- Vs. Postoperative Thromboprophylaxis in Pancreatic Surgery
NCT05255003PHASE4RECRUITINGSTrategies for Anticoagulation in Patients With thRombocytopenia and Cancer-associated Thrombosis
NCT07361679PHASE4RECRUITINGLDA and LMWH vs LDA Alone in High-risk Patients for Preeclampsia Prevention
NCT00407641PHASE4WITHDRAWNEffects of Tinzaparin on Cardio-vascular Outcomes and on Blood Lipids in Diabetic Patients on Chronic Hemodialysis
NCT00689520PHASE4COMPLETEDLong-Term Low-Molecular-Weight Heparin Versus Oral Anticoagulants in Deep Venous Thrombosis
NCT00711308PHASE4COMPLETEDTinzaparin in the Treatment of the Acute Pulmonary Embolism
NCT00851864PHASE4COMPLETEDSafety and Efficacy of Therapeutic Anticoagulation With Tinzaparin During Pregnancy Via Weight-based Dosing
NCT01390051PHASE4COMPLETEDCan Low Molecular Weight Heparin During Pregnancy With Intrauterine Growth Restriction Increase Birth Weight?
NCT01930396PHASE4COMPLETEDUse of Tinzaparin for Anticoagulation in Hemodialysis
NCT03614741PHASE4UNKNOWNEfficacy, Safety and Pharmacokinetics of Tinzaparin During Slow Low Efficient Daily Dialysis in Intensive Care Patients
NCT04794569PHASE4TERMINATEDTinzaparin Lead-In to Prevent the Post-Thrombotic Syndrome
NCT00225108PHASE2/PHASE3COMPLETEDThe STOP CLOT Pilot Study: Study of Low Molecular Weight Heparin in High Risk Cesarean Section
NCT00475098PHASE3COMPLETEDEffect of Low Molecular Weight Heparin: Tinzaparin in Lung Tumours (TILT)
NCT00628576PHASE3COMPLETEDEvaluation of Long-Term Sequelae After Thrombophlebitis, i.e. Deep Venous Thrombosis of the Lower Extremities
NCT01455831PHASE3COMPLETEDExtended Peri-operative Tinzaparin to Improve Disease-free Survival in Patients With Resectable Colorectal Cancer
NCT03240120PHASE3UNKNOWNA Study of Dabigatran Etexilate as Primary Treatment of Malignancy Associated Venous Thromboembolism
NCT05625932PHASE3COMPLETEDTINzaparin Prophylaxis in Patients With Metastatic Colorectal Cancer
NCT02260414PHASE2COMPLETEDEffects of Anticoagulant Preventive Injection in Patients With Blood Cancer
NCT04808882PHASE2COMPLETEDANTIcoagulation in Severe COVID-19 Patients
NCT04741464Not specifiedACTIVE_NOT_RECRUITINGEffect of Tinzaparin on Inflammatory Biomarkers During the Acute Phase of Deep Vein Thrombosis
NCT07559643Not specifiedNOT_YET_RECRUITINGThe OAT Trail: The Obesity Anti-Coagulation Thromboprophylaxis Trial.
NCT00135863Not specifiedTERMINATEDMesoHep II: Intraperitoneal Low Molecular Weight Heparin in Peritoneal Dialysis
NCT00186745Not specifiedTERMINATEDUse of Low Molecular Weight Heparin (Tinzaparin) to Treat Blood Clots in Patients With Kidney Failure
NCT00967148Not specifiedCOMPLETEDThromboprophylaxis for Patients Undergoing Surgical Resection for Colon Cancer
NCT01321788Not specifiedUNKNOWNVenous Thromboembolism Prophylaxis Post Cesarean Section
NCT02719418Not specifiedCOMPLETEDStudy of the Bioaccumulation of Tinzaparin in Renally Impaired Patients When Given at Prophylactic Doses
NCT03099031Not specifiedCOMPLETEDNon Interventional Study of the Validation of the Ottawa Score in Cancer Patients With Venous Thromboembolism (VTE)
NCT04730856Not specifiedCOMPLETEDStandard vs High Prophylactic Doses or Anticoagulation in Patients With High Risk of Thrombosis Admitted With COVID-19 Pneumonia (PROTHROMCOVID)
NCT05036824Not specifiedUNKNOWNIntensive Dose Tinzaparin in Hospitalized COVID-19 Patients

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

2 molecules share ≥1 primary target. Top 2 by shared-target count:

MoleculeSourceStatusShared targets
IDRAPARINUXChEMBLPhase 3SERPINC1
fondaparinuxPubChemApprovedSERPINC1