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May 5
First Low-Molecular-Weight Heparin for Extended Treatment to Reduce the Recurrence of Blood Clots in Patients with Cancer: FRAGMIN®, Approved by the USFDA

The USFDA has approved a new indication for FRAGMIN® (dalteparin sodium injection): extended treatment of symptomatic venous thromboembolism (VTE) [proximal deep vein thrombosis (DVT) and/or pulmonary embolism (PE)] to reduce the recurrence of VTE in cancer patients.

In the United States, FRAGMIN is also indicated for the following:

  • Fragmin.jpgprevention of DVT, which may lead to PE (pulmonary embolism), in patients undergoing hip replacement surgery, in at- risk patients undergoing abdominal surgery and in at-risk acutely ill patients whose mobility is severely restricted
  • prophylaxis of ischemic complications resulting from unstable angina and non- Q-wave myocardial infarction (heart attack), when used with aspirin

Exclusively licensed by Eisai, Inc. from Pfizer, Inc. for U.S. distribution, FRAGMIN® is the first low-molecular- weight heparin (LMWH) approved in the U.S. for the extended treatment of recurrent VTE in patients with cancer.

Find more details from the full report.


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« USFDA Awarded Orphan Drug Grant to Expression Genetics, Inc. for Clinical Development of EGEN-001 for Ovarian Cancer Treatment | Main | Abbott’s Investigational Treatment ABT-874 Passed Phase II Psoriasis Study »

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