Target intelligence / Profile preview

Hypercoagulability

Molecular classification
Not applicable (Physiological condition/Clinical state)
01

Overview

Hypercoagulability, also known as thrombophilia, is a clinical condition characterized by an abnormally increased tendency for blood to clot within the vascular system (StatPearls, 2023). It is not a specific molecular target (such as a single receptor or enzyme) but rather a complex physiological state resulting from an imbalance between procoagulant and anticoagulant factors (PubMed, 2021). This prothrombotic state can be inherited, such as through Factor V Leiden or Protein C deficiency, or acquired due to factors like malignancy, pregnancy, or prolonged immobilization (Mayo Clinic, 2023). The condition significantly increases the risk of life-threatening events, including deep vein thrombosis (DVT), pulmonary embolism (PE), and stroke. Therapeutic management focuses on using anticoagulant drugs that target specific enzymes within the coagulation cascade, such as Factor Xa or Thrombin (Factor IIa), to prevent thrombus formation and maintain vascular patency (PubChem, 2024).

Other names
ThrombophiliaProthrombotic stateHypercoagulable stateClotting disorder
02

Mechanism of action

Pharmacological intervention aims to inhibit key proteases in the coagulation cascade (specifically Factor Xa and Thrombin) to decrease fibrin formation and prevent the propagation of blood clots (PubChem, 2024).

03

Biological functions

Blood coagulationHemostasisThrombosis
04

Disease associations

Venous thromboembolism (VTE)Deep vein thrombosis (DVT)Pulmonary embolism (PE)StrokeMyocardial infarctionPregnancy complications (e.g., recurrent miscarriage)
05

Safety considerations

Major bleeding (hemorrhage)Intracranial hemorrhageGastrointestinal bleedingHeparin-induced thrombocytopenia (HIT)Drug-drug interactions (especially with cytochrome P450 inhibitors/inducers)
06

Interacting drugs

Warfarin

7 more in the full profile.

07

Biomarkers

D-dimer (StatPearls, 2023)Prothrombin Time (PT)Activated Partial Thromboplastin Time (aPTT)Protein C activityProtein S activityAntithrombin III levelsFactor V Leiden (G1691A) mutationProthrombin G20210A mutation

Beyond the preview

Go deeper on Hypercoagulability.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Hypercoagulability.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call