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Tinzaparin sodium

Alternative Names: tinzaparin sodium, tinzaparin, innohep
Latest Update: 2024-11-28
Latest Update Note: Clinical Trial Update

Product Description

Tinzaparin is a low-molecular-weight heparin (LMWH) with antithrombotic properties. It has FDA-approved labeling for use in the treatment of acute symptomatic deep-vein thrombosis (DVT) with or without pulmonary embolism (PE) when administered in conjunction with warfarin sodium (Sourced from: https://pubmed.ncbi.nlm.nih.gov/12166042/)

Mechanisms of Action: Thrombin Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Subcutaneous

FDA Designation: None *

Approval Status: Approved

Approved Countries: Algeria | Austria | Belgium | Canada | Chile | Colombia | Cyprus | Denmark | Egypt | Finland | France | Germany | Greece | Hong Kong | Ireland | Italy | Jordan | Luxembourg | Malaysia | Morocco | Netherlands | New Zealand | Pakistan | Peru | Philippines | Portugal | Romania | Saudi Arabia | Slovenia | South Africa | Spain | Sweden | Taiwan | Thailand | Tunisia | Turkey | United Kingdom

Approved Indications: None

Known Adverse Events: None

Company: LEO Pharma
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Tinzaparin sodium

Countries in Clinic: Spain

Active Clinical Trial Count: 2

Highest Development Phases

Phase 3: Colorectal Cancer|Thromboembolism

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

PROTINCOL

P3

Active, not recruiting

Colorectal Cancer

2025-03-23

PROTINCOL

P3

Recruiting

Thromboembolism|Colorectal Cancer

2024-12-01

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