Daiichi Sankyo Europe GmbH

Edoxaban Demonstrates Superior Efficacy Compared With Enoxaparin Sodium in Preventing VTE After Total Knee Replacement

    Tokyo, July 12, 2010 (ots/PRNewswire) - Daiichi Sankyo Company, Limited announced that its investigational once-daily oral, direct factor Xa inhibitor, edoxaban, was shown to be superior to enoxaparin in preventing venous thromboembolic (VTE) events in patients following total knee replacement (TKR), a type of major orthopedic surgery. Results from the Phase III STARS E-3 (Studying Thrombosis After Replacement Surgery) study were presented at the 21st International Congress on Thrombosis (ICT) in Milan, Italy.[i]

    This multicenter, double-blind, double dummy, centrally randomized trial evaluated the efficacy and safety of edoxaban compared with enoxaparin in patients undergoing TKR in Japan and Taiwan. A total of 716 patients received either 30 mg once-daily oral dose of edoxaban or subcutaneous injection of enoxaparin 2,000 international units (equivalent to 20 mg) twice-daily for 11 to 14 days. The primary efficacy endpoint of the trial was the incidence of symptomatic pulmonary embolism (PE) and symptomatic and asymptomatic deep vein thrombosis (DVT). The primary safety endpoint was the incidence of major bleeding and clinically relevant non-major bleeding.

    DVT occurred in 7.4 percent of patients receiving edoxaban once-daily compared with 13.9 percent of patients who received enoxaparin (relative risk reduction of 46.8 percent; p=0.01). There were no PE events observed in either treatment group. There was no statistically significant difference in major and clinically relevant non-major bleeding (p=0.13). There were no cases of intracranial hemorrhage or death in either treatment group.

    Indicators for potential liver damage in both treatment groups were carefully monitored during this trial by measuring bilirubin and serum aminotransferase levels.[ii] Elevations greater than three times the upper limit of the normal range of serum aminotransferase levels occurred in 1.4 percent of patients taking edoxaban compared with 8.0 percent of those taking enoxaparin.

    "The combination of efficacy, tolerability and convenient once-daily oral dosing in this clinical setting further supports the potential role of edoxaban in helping patients and physicians avoiding thrombotic events," said Dr. Takeshi Fuji, Head of Orthopedic Surgery, Osaka Koseinenkin Hospital. "These results are encouraging as they demonstrate superior efficacy of once-daily edoxaban compared with twice daily subcutaneous enoxaparin, the current standard of care for this patient population."

    In March 2010, Daiichi Sankyo submitted a New Drug Application to the Ministry of Health, Labor and Welfare in Japan seeking approval of edoxaban for the prevention of VTE after major orthopedic surgery.

    Global Development of Edoxaban  

    The global clinical development program for edoxaban comprises several indications, including the prevention of stroke and systemic embolic events in patients with atrial fibrillation, as well as the acute treatment and long-term secondary prevention of VTE.

@@start.t1@@      Global studies include:
      - ENGAGE AF-TIMI 48: Investigates two different doses of once-daily
         edoxaban versus warfarin in approximately 20,500 patients with atrial
         fibrillation for the prevention of stroke and systemic embolic events.
         ENGAGE AF-TIMI 48 began enrollment in late 2008 and is expected to be
         completed in 2012.
      - HOKUSAI VTE: To date, the largest single trial for the secondary
         prevention of recurrent VTE in approximately 7,500 patients with deep
         vein thrombosis and/or pulmonary embolism as well as for the acute
         treatment of VTE. HOKUSAI VTE trial enrollment began in early 2010.@@end@@

    Both HOKUSAI VTE and ENGAGE AF-TIMI 48 are Phase III, multi-national, randomized, double-blind studies.

    About Edoxaban  

    Edoxaban is a once-daily oral anticoagulant that directly inhibits factor Xa, an important factor in the coagulation process. Daiichi Sankyo is developing edoxaban as a potential new treatment for the prevention of both arterial and venous thromboembolism. Notably, Daiichi Sankyo has more than 25 years experience conducting research in the area of factor Xa inhibition, and was the first company to study these compounds in humans. Edoxaban is being developed solely by Daiichi Sankyo.


    DAIICHI SANKYO is a global pharmaceutical company that focuses on researching and marketing innovative medications. The company was created in 2005 through the merger of two traditional Japanese enterprises, Daiichi and Sankyo. With net sales of nearly 7.3 billion EUR in fiscal year 2009 (as of March 31st), DAIICHI SANKYO is one of the world's 20 leading pharmaceutical companies. The company's world headquarters is in Tokyo, its European base is located in Munich. DAIICHI SANKYO has affiliates in 12 European countries and has been one of the strongest Japanese pharmaceutical companies located in Europe since it set up European production facilities and marketing offices in 1990. The company's research activities focus on the areas of cardiovascular diseases, hematology, anti-infectives and cancer. Its aim is to develop medications that are "best" in their class or to create new classes of pharmaceutical drugs.

    Forward-looking statements  

    This press release contains forward-looking statements and information about future developments in the sector, and the legal and business conditions of DAIICHI SANKYO, Co. Ltd, DAIICHI SANKYO, Inc., and DAIICHI SANKYO EUROPE GmbH. Such forward-looking statements are uncertain and are subject at all times to the risks of change, particularly to the usual risks faced by a global pharmaceutical company, including the impact of the prices for products and raw materials, medication safety, changes in exchange rates, government regulations, employee relations, taxes, political instability and terrorism as well as the results of independent demands and governmental inquiries that affect the affairs of the company. All forward-looking statements contained in this release hold true as of the date of publication. They do not represent any guarantee of future performance. Actual events and developments could differ materially from the forward-looking statements that are explicitly expressed or implied in these statements. DAIICHI SANKYO, Co. Ltd, DAIICHI SANKYO, Inc., and DAIICHI SANKYO EUROPE GmbH assume no responsibility for the updating of such forward-looking statements about future developments of the sector, legal and business conditions and the company.

@@start.t2@@      ---------------------------------
      [i] T. Fuji et al., Edoxaban versus enoxaparin for thromboprophylaxis
            after total knee replacement: The STARS E-3 trial 21st International
            Congress of Thrombosis, July 6 - 9 2010, Milano.
      [ii]Liver Blood Tests. Available at:
            Accessed June 18, 2010.@@end@@

ots Originaltext: Daiichi Sankyo Europe GmbH
Im Internet recherchierbar: http://www.presseportal.ch

CONTACT:  For more information, please contact: Toshiaki Sai,
DaiichiSankyo, Co., Ltd. (Japan), +81-3-6225-1126 (office). Dr.
MichaelaPaudler-Debus, Daiichi Sankyo Europe GmbH,
+49-(0)89-78-08-685  (office),+49-(0)172-845-8974  (mobile)

Weitere Meldungen: Daiichi Sankyo Europe GmbH

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