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Daiichi Sankyo Europe: New two-years follow-up data from ETNA-AF-Europe reaffirms benefit of LIXIANA (edoxaban) in people with atrial fibrillation


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Large routine clinical practice study, ETNA-AF-Europe, demonstrates continued benefits of edoxaban across age groups and supports treatment in elderly patient populations, in line with those observed in ETNA-AF after one year and in ENGAGE AF-TIMI 48
ETNA-AF-Europe is part of the global ETNA-AF programme, which is the largest prospective, non-interventional study investigating a single non-vitamin K antagonist oral anticoagulant (NOAC) to date
Data presented at the annual scientific meeting of the European Heart Rhythm Association
Daiichi Sankyo Europe, (hereafter, Daiichi Sankyo) today announced the presentation of new routine clinical practice outcomes data confirming, in line with the randomised clinical trial data, the consistent effectiveness and safety profile of LIXIANA ....

Noord Holland , The Netherlands , Wolfgang Schiessl , Daiichi Sankyo , Garth Virgin , Daiichi Sankyo Europe , Daiichi Sankyo Europe Gmb , European Heart Rhythm Association , Atrial Fibrillation At University Of Amsterdam , Affairs Specialty Medicines At Daiichi Sankyo Europe , Amsterdam University Medical Centers , Daiichi Sankyo Group , Portfolio Communications , Edoxaban Clinical Research Programme , Sankyo Europe , Cardiac Electrophysiology , Atrial Fibrillation , Edoxaban Treatment , Sankyo Group , Pharma Innovator , Competitive Advantage , Sankyo Europe Gmbh , Cardiovascular Europe , நூற்த் ஹாலண்ட் , தி நெதர்லாந்து , தய்ச்சி சாங்கியோ ,

New two-years follow-up data from ETNA-AF-Europe reaffirms benefit of LIXIANA® (edoxaban) in people with atrial fibrillation


New two-years follow-up data from ETNA-AF-Europe reaffirms benefit of LIXIANA® (edoxaban) in people with atrial fibrillation
04/26/2021 | 03:01am EDT
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Large routine clinical practice study, ETNA-AF-Europe, demonstrates continued benefits of edoxaban across age groups and supports treatment in elderly patient populations, in line with those observed in ETNA-AF after one year and in ENGAGE AF-TIMI 48
ETNA-AF-Europe is part of the global ETNA-AF programme, which is the largest prospective, non-interventional study investigating a single non-vitamin K antagonist oral anticoagulant (NOAC) to date
Data presented at the annual scientific meeting of the European Heart Rhythm Association
Daiichi Sankyo Europe, (hereafter, Daiichi Sankyo) today announced the presentation of new routine clinical practice outcomes data confirming, in line with the randomised clinical trial data, the consistent effectiveness and safety pr ....

Noord Holland , The Netherlands , Daiichi Sankyo , Garth Virgin , Daiichi Sankyo Europe , European Heart Rhythm Association , Atrial Fibrillation At University Of Amsterdam , Affairs Specialty Medicines At Daiichi Sankyo Europe , Amsterdam University Medical Centers , Daiichi Sankyo Group , Edoxaban Clinical Research Programme , Cardiac Electrophysiology , Atrial Fibrillation , Edoxaban Treatment , Sankyo Group , Pharma Innovator , Competitive Advantage , நூற்த் ஹாலண்ட் , தி நெதர்லாந்து , தய்ச்சி சாங்கியோ , தய்ச்சி சாங்கியோ யூரோப் , ஐரோப்பிய இதயம் தாளம் சங்கம் , ஆம்ஸ்டர்டாம் பல்கலைக்கழகம் மருத்துவ மையங்கள் , தய்ச்சி சாங்கியோ குழு , இதய மின் இயற்பியல் , ஏட்ரியல் குறு நடுக்கம் ,

Daiichi Sankyo UK, Limited: ENHERTU - (TRASTUZUMAB DERUXTECAN) NOW AVAILABLE VIA THE CANCER DRUGS FUND FOR THE TREATMENT OF HER2 POSITIVE METASTATIC BREAST CANCER


Daiichi Sankyo UK, Limited: ENHERTU - (TRASTUZUMAB DERUXTECAN) NOW AVAILABLE VIA THE CANCER DRUGS FUND FOR THE TREATMENT OF HER2 POSITIVE METASTATIC BREAST CANCER
Reimbursement decisions in Scotland, Wales, and Northern Ireland to be announced later this year
Daiichi Sankyo UK, Limited
(hereafter, Daiichi Sankyo) and AstraZeneca UK today welcome the news that the National Institute for Health and Care Excellence (NICE) has recommended Enhertu
(trastuzumab deruxtecan) for use within the Cancer Drugs Fund (CDF) as an option for treating HER2 positive unresectable or metastatic breast cancer in adults who have received two or more prior anti-HER2 based therapies.
In the UK, almost 54,000 cases of breast cancer in women are diagnosed annually, with an estimated one in five cases being HER2 positive. ....

United Kingdom , Northern Ireland , Daiichi Sankyo , Jo Taylor , Iqbaln Iqbal , Melo Gagliato , Alistair Gordon , Haran Maheson , Karun Krishna , Peter Schmid , England Cancer Drugs Fund , Daichi Sankyo United Kingdom Ltd , World Health Organization , Government Affairs , National Institute For Health , Cancer Drugs Fund , Corporate Communications , Daiichi Sankyo Group , National Comprehensive Cancer Network , Barts Cancer Institute , Scottish Medicines Consortium , For United Kingdom , Sankyo United Kingdom , Astrazeneca United Kingdom , National Institute , Care Excellence ,

ENHERTU® ▼ (TRASTUZUMAB DERUXTECAN) NOW AVAILABLE VIA THE CANCER DRUGS FUND FOR THE TREATMENT OF HER2 POSITIVE METASTATIC BREAST CANCER


Press release content from Business Wire. The AP news staff was not involved in its creation.
ENHERTU® ▼ (TRASTUZUMAB DERUXTECAN) NOW AVAILABLE VIA THE CANCER DRUGS FUND FOR THE TREATMENT OF HER2 POSITIVE METASTATIC BREAST CANCER
April 20, 2021 GMT
Daiichi Sankyo UK, Limited
(hereafter, Daiichi Sankyo) and AstraZeneca UK today welcome the news that the National Institute for Health and Care Excellence (NICE) has recommended Enhertu ® (trastuzumab deruxtecan) for use within the Cancer Drugs Fund (CDF) as an option for treating HER2 positive unresectable or metastatic breast cancer in adults who have received two or more prior anti-HER2 based therapies.
In the UK, almost 54,000 cases of breast cancer in women are diagnosed annually, with an estimated one in five cases being HER2 positive. 1,2,3 The impact of the disease is significant, with breast cancer responsible for approximately 12,000 deaths per year. 1 There are an estimated 35,000 people living with ....

United Kingdom , Daiichi Sankyo , Jo Taylor , Iqbaln Iqbal , Melo Gagliato , Alistair Gordon , Haran Maheson , Karun Krishna , Peter Schmid , England Cancer Drugs Fund , Daichi Sankyo United Kingdom Ltd , World Health Organization , Government Affairs , National Institute For Health , Cancer Drugs Fund , Corporate Communications , Daiichi Sankyo Group , National Comprehensive Cancer Network , Barts Cancer Institute , Scottish Medicines Consortium , Sankyo United Kingdom , Astrazeneca United Kingdom , National Institute , Care Excellence , Professor Peter Schmid , Barts Cancer ,

Daiichi Sankyo Company, Limited: Phase 1/2 Trial Initiated for Daiichi Sankyo's Menin Inhibitor DS-1594 in Patients with Acute Myeloid Leukemia and Acute Lymphoblastic Leukemia


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Daiichi Sankyo Company, Limited (hereafter Daiichi Sankyo) today announced the first patient has been dosed in the first-in-human phase 1/2 study of DS-1594, a selective small-molecule menin inhibitor, in adults with relapsed/refractory acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). The trial is being conducted by The University of Texas MD Anderson Cancer Center under an existing strategic research collaboration.
Inhibition of the menin protein is being studied as a novel treatment approach for acute leukemias with MLL rearrangement (MLLr) or NPM1 mutation (NPM1m), two gene alterations that drive cancer development and growth.
1 MLLr occurs in approximately 5 to 10% of acute leukemia patients and is associated with aggressive disease, reduced treatment response and poor prognosis. ....

United States , Masashi Kawase , Arnaud Lesegretain , Daiichi Sankyo , Daiichi Sankyo Europe Gmb , Jennifer Brennan , Daiichi Sankyo Co Ltd , Plexxikon Inc , Daiichi Sankyo Inc , Daiichi Sankyo Company , University Of Texas Md Anderson Cancer Center , Daiichi Sankyo Group , Leukemia Lymphoma Society , Cancer Center , Vice President , Alpha Portfolio , Acute Myeloid Leukemia , Acute Lymphoblastic Leukemia , Daiichi Sankyo Cancer Enterprise , Sankyo Group , Pharma Innovator , Competitive Advantage , Population Fact Sheet , Updated November , Leukemia Facts , Acute Myeloid ,