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Intermediate dose nadroparin

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · FDA-approved active Small molecule

Nadroparin is a low-molecular-weight heparin that inhibits blood coagulation by enhancing the activity of antithrombin III against factor Xa and thrombin.

Nadroparin is a low-molecular-weight heparin that inhibits blood coagulation by enhancing the activity of antithrombin III against factor Xa and thrombin. Used for Thromboprophylaxis in surgical patients, Treatment of deep vein thrombosis, Treatment of pulmonary embolism.

At a glance

Generic nameIntermediate dose nadroparin
Also known asnadroparin, Fraxiparin
SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Drug classLow-molecular-weight heparin (LMWH)
TargetFactor Xa, Thrombin (via antithrombin III enhancement)
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Nadroparin is derived from unfractionated heparin through chemical depolymerization, resulting in a mixture of polysaccharide chains with molecular weights between 4,000 and 6,000 Da. It potentiates antithrombin III-mediated inhibition of activated factor X (factor Xa) more than thrombin, providing anticoagulant activity with a favorable pharmacokinetic profile for subcutaneous administration. The intermediate dose formulation is used for thromboprophylaxis and treatment of thromboembolic disorders.

Approved indications

Common side effects

Key clinical trials

Primary sources

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