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Subcutaneous enoxaparin sodium

Zhongshan Hospital (Xiamen), Fudan University · Phase 3 active Small molecule

Enoxaparin sodium is a low-molecular-weight heparin that inhibits blood coagulation by enhancing the activity of antithrombin III against factors Xa and IIa.

Enoxaparin sodium is a low-molecular-weight heparin that inhibits blood coagulation by enhancing the activity of antithrombin III against factors Xa and IIa. Used for Prophylaxis of venous thromboembolism, Treatment of acute deep vein thrombosis, Treatment of acute pulmonary embolism.

At a glance

Generic nameSubcutaneous enoxaparin sodium
Also known asLovenox, experimental
SponsorZhongshan Hospital (Xiamen), Fudan University
Drug classLow-molecular-weight heparin (LMWH)
TargetCoagulation factors Xa and IIa (via antithrombin III enhancement)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhasePhase 3

Mechanism of action

Enoxaparin is derived from unfractionated heparin and works by potentiating antithrombin III, a natural anticoagulant. This leads to inactivation of coagulation factors Xa and IIa (thrombin), preventing thrombus formation. The subcutaneous formulation provides predictable pharmacokinetics and is used for both prophylaxis and treatment of thromboembolism.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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