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	<title>PR Hub &#187; Daiichi-Sankyo</title>
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	<link>http://pr.gaeatimes.com</link>
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	<pubDate>Mon, 21 Nov 2011 13:29:44 +0000</pubDate>
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		<title>First 3-in-1 Blood Pressure Pill now Available in the UK</title>
		<link>http://pr.gaeatimes.com/first-3-in-1-blood-pressure-pill-now-available-in-the-uk-53721/</link>
		<comments>http://pr.gaeatimes.com/first-3-in-1-blood-pressure-pill-now-available-in-the-uk-53721/#comments</comments>
		<pubDate>Mon, 21 Nov 2011 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Business]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[New Products / Services]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[London]]></category>

		<category><![CDATA[November 22]]></category>

		<category><![CDATA[United Kingdom]]></category>

		<guid isPermaLink="false">http://pr.gaeatimes.com/first-3-in-1-blood-pressure-pill-now-available-in-the-uk-53721/</guid>
		<description><![CDATA[LONDON, November 22, 2011  -
Sevikar HCT®&#9660; combines three treatments in one reducing the number of tablets patients take to manage high blood pressure

Today Daiichi Sankyo UK announces that it has launched Sevikar HCT, the first three-in-one pill in the UK to treat high blood pressure.[1] This condition affects around 8.5 million people in the .... Source article on Gaea Times at  &nbsp;: <a href="http://pr.gaeatimes.com/first-3-in-1-blood-pressure-pill-now-available-in-the-uk-53721/">First 3-in-1 Blood Pressure Pill now Available in the UK</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/first-3-in-1-blood-pressure-pill-now-available-in-the-uk-53721/feed/</wfw:commentRss>
		</item>
		<item>
		<title>European Survey Highlights the Risk to Patients Caused by Inconsistency in Hypertension Management</title>
		<link>http://pr.gaeatimes.com/european-survey-highlights-the-risk-to-patients-caused-by-inconsistency-in-hypertension-management-47691/</link>
		<comments>http://pr.gaeatimes.com/european-survey-highlights-the-risk-to-patients-caused-by-inconsistency-in-hypertension-management-47691/#comments</comments>
		<pubDate>Fri, 08 Jul 2011 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Business]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Surveys / Polls / Research]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[Germany]]></category>

		<category><![CDATA[July 8]]></category>

		<category><![CDATA[Munich]]></category>

		<guid isPermaLink="false">http://pr.gaeatimes.com/european-survey-highlights-the-risk-to-patients-caused-by-inconsistency-in-hypertension-management-47691/</guid>
		<description><![CDATA[MUNICH, July 8, 2011  -

For distribution to consumer and medical media

- Findings From the Supporting Hypertension Awareness and
Research Europe-wide (SHARE) Survey Suggest the Need to Implement a
Consistent Strategy to Improve and Maintain Blood Pressure
Control
Physicians&#8217; treatment approaches to hypertension management are
inconsistent[1] despite ESH-ESC (European Society of
Hypertension and European Society of Cardiology) arterial
hypertension guidelines[2], which could .... Original article &nbsp;: <a href="http://pr.gaeatimes.com/european-survey-highlights-the-risk-to-patients-caused-by-inconsistency-in-hypertension-management-47691/">European Survey Highlights the Risk to Patients Caused by Inconsistency in Hypertension Management</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/european-survey-highlights-the-risk-to-patients-caused-by-inconsistency-in-hypertension-management-47691/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Global Phase III Trial With Selective c-MET Inhibitor Tivantinib (ARQ 197) Starts Enrolling Patients in Europe</title>
		<link>http://pr.gaeatimes.com/global-phase-iii-trial-with-selective-c-met-inhibitor-tivantinib-arq-197-starts-enrolling-patients-in-europe-44124/</link>
		<comments>http://pr.gaeatimes.com/global-phase-iii-trial-with-selective-c-met-inhibitor-tivantinib-arq-197-starts-enrolling-patients-in-europe-44124/#comments</comments>
		<pubDate>Mon, 18 Apr 2011 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Medical Equipment]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[April 18]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[Germany]]></category>

		<category><![CDATA[Munich]]></category>

		<guid isPermaLink="false">http://pr.gaeatimes.com/global-phase-iii-trial-with-selective-c-met-inhibitor-tivantinib-arq-197-starts-enrolling-patients-in-europe-44124/</guid>
		<description><![CDATA[MARQUEE Trial to Study Tivantinib in Advanced, Non-squamous, Non-small Cell Lung Cancer

MUNICH, April 18, 2011  - Daiichi Sankyo announced today that it has begun
enrolling patients in Europe into a large, multinational phase III trial of
tivantinib (ARQ 197). Tivantinib is an investigational small molecule
inhibitor of the c-MET receptor tyrosine kinase in final phase of clinical
development .... Original source &nbsp;: <a href="http://pr.gaeatimes.com/global-phase-iii-trial-with-selective-c-met-inhibitor-tivantinib-arq-197-starts-enrolling-patients-in-europe-44124/">Global Phase III Trial With Selective c-MET Inhibitor Tivantinib (ARQ 197) Starts Enrolling Patients in Europe</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/global-phase-iii-trial-with-selective-c-met-inhibitor-tivantinib-arq-197-starts-enrolling-patients-in-europe-44124/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Daiichi Sankyo and ArQule Enroll First Non-Small Cell Lung Cancer Patient Into Global Phase III Trial for ARQ 197</title>
		<link>http://pr.gaeatimes.com/daiichi-sankyo-and-arqule-enroll-first-non-small-cell-lung-cancer-patient-into-global-phase-iii-trial-for-arq-197-39978/</link>
		<comments>http://pr.gaeatimes.com/daiichi-sankyo-and-arqule-enroll-first-non-small-cell-lung-cancer-patient-into-global-phase-iii-trial-for-arq-197-39978/#comments</comments>
		<pubDate>Wed, 12 Jan 2011 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[January 12]]></category>

		<category><![CDATA[Japan]]></category>

		<category><![CDATA[Massachusetts]]></category>

		<category><![CDATA[Tokyo And Woburn]]></category>

		<category><![CDATA[United States of America]]></category>

		<guid isPermaLink="false">http://pr.gaeatimes.com/daiichi-sankyo-and-arqule-enroll-first-non-small-cell-lung-cancer-patient-into-global-phase-iii-trial-for-arq-197-39978/</guid>
		<description><![CDATA[TOKYO and WOBURN, Massachusetts, January 12, 2011  - Daiichi Sankyo Company, Limited (TSE 4568) and ArQule, Inc. (Nasdaq:
ARQL) today announced that the first patient has been enrolled in the phase
III trial of ARQ 197, an investigational selective inhibitor of the c-Met
receptor tyrosine kinase, in combination with erlotinib, for patients
diagnosed with non-squamous, non-small cell lung ... Read the original article on Gaea Times at  : <a href="http://pr.gaeatimes.com/daiichi-sankyo-and-arqule-enroll-first-non-small-cell-lung-cancer-patient-into-global-phase-iii-trial-for-arq-197-39978/">Daiichi Sankyo and ArQule Enroll First Non-Small Cell Lung Cancer Patient Into Global Phase III Trial for ARQ 197</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/daiichi-sankyo-and-arqule-enroll-first-non-small-cell-lung-cancer-patient-into-global-phase-iii-trial-for-arq-197-39978/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Daiichi Sankyo Announces First European Approval for Sevikar HCT(R), a New Three-in-one Combination Product for the Treatment of High Blood Pressure*</title>
		<link>http://pr.gaeatimes.com/daiichi-sankyo-announces-first-european-approval-for-sevikar-hctr-a-new-three-in-one-combination-product-for-the-treatment-of-high-blood-pressure-39406/</link>
		<comments>http://pr.gaeatimes.com/daiichi-sankyo-announces-first-european-approval-for-sevikar-hctr-a-new-three-in-one-combination-product-for-the-treatment-of-high-blood-pressure-39406/#comments</comments>
		<pubDate>Mon, 20 Dec 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[December 20]]></category>

		<category><![CDATA[Germany]]></category>

		<category><![CDATA[Munich]]></category>

		<guid isPermaLink="false">http://pr.gaeatimes.com/daiichi-sankyo-announces-first-european-approval-for-sevikar-hctr-a-new-three-in-one-combination-product-for-the-treatment-of-high-blood-pressure-39406/</guid>
		<description><![CDATA[New Treatment Option Contributes to Fight Against Hypertension, Which Affects over 30% of Adults in Europe(1)

MUNICH, December 20, 2010  - Daiichi Sankyo Europe announced today that Sevikar HCT(R) is
now approved in Germany, the first market to launch this new once-daily
three-in-one combination product for the treatment of high blood pressure
(BP). This new drug combines the ... Read the original article on Gaea Times at  : <a href="http://pr.gaeatimes.com/daiichi-sankyo-announces-first-european-approval-for-sevikar-hctr-a-new-three-in-one-combination-product-for-the-treatment-of-high-blood-pressure-39406/">Daiichi Sankyo Announces First European Approval for Sevikar HCT(R), a New Three-in-one Combination Product for the Treatment of High Blood Pressure*</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/daiichi-sankyo-announces-first-european-approval-for-sevikar-hctr-a-new-three-in-one-combination-product-for-the-treatment-of-high-blood-pressure-39406/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Daiichi Sankyo Completes Enrollment of the Edoxaban Global Phase III ENGAGE AF-TIMI 48 Study in Patients With Atrial Fibrillation</title>
		<link>http://pr.gaeatimes.com/daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38694/</link>
		<comments>http://pr.gaeatimes.com/daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38694/#comments</comments>
		<pubDate>Wed, 01 Dec 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[December 1]]></category>

		<category><![CDATA[London]]></category>

		<category><![CDATA[United Kingdom]]></category>

		<guid isPermaLink="false">http://pr.gaeatimes.com/daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38694/</guid>
		<description><![CDATA[More Than 21,000 Patients Enrolled in the Largest Clinical Study With a Factor Xa Inhibitor

LONDON, December 1, 2010  - Daiichi Sankyo Company, Limited (TSE: 4568), announced today that it has
successfully completed patient enrollment for its phase III ENGAGE AF-TIMI 48
clinical study of edoxaban, a direct, specific, oral Factor Xa inhibitor that
is being investigated in ... <a href="http://pr.gaeatimes.com/daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38694/" title="Daiichi Sankyo Completes Enrollment of the Edoxaban Global Phase III ENGAGE AF-TIMI 48 Study in Patients With Atrial Fibrillation">Read more >></a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38694/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Update: Daiichi Sankyo Completes Enrollment of the Edoxaban Global Phase III ENGAGE AF-TIMI 48 Study in Patients With Atrial Fibrillation</title>
		<link>http://pr.gaeatimes.com/update-daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38712/</link>
		<comments>http://pr.gaeatimes.com/update-daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38712/#comments</comments>
		<pubDate>Wed, 01 Dec 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[December 1]]></category>

		<category><![CDATA[Tokyo]]></category>

		<category><![CDATA[United Kingdom]]></category>

		<guid isPermaLink="false">http://pr.gaeatimes.com/update-daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38712/</guid>
		<description><![CDATA[More Than 21,000 Patients Enrolled in the Largest Clinical Study with a Factor Xa Inhibitor

TOKYO, December 1, 2010  - Daiichi Sankyo Company, Limited (TSE: 4568), announced today
that it has successfully completed patient enrollment for its phase III
ENGAGE AF-TIMI 48 clinical study of edoxaban, a direct, specific, oral Factor
Xa inhibitor that is being investigated in ... <a href="http://pr.gaeatimes.com/update-daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38712/" title="Update: Daiichi Sankyo Completes Enrollment of the Edoxaban Global Phase III ENGAGE AF-TIMI 48 Study in Patients With Atrial Fibrillation">Read more >></a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/update-daiichi-sankyo-completes-enrollment-of-the-edoxaban-global-phase-iii-engage-af-timi-48-study-in-patients-with-atrial-fibrillation-38712/feed/</wfw:commentRss>
		</item>
		<item>
		<title>ArQule and Daiichi Sankyo Expand Drug Discovery Collaboration in Oncology</title>
		<link>http://pr.gaeatimes.com/arqule-and-daiichi-sankyo-expand-drug-discovery-collaboration-in-oncology-36422/</link>
		<comments>http://pr.gaeatimes.com/arqule-and-daiichi-sankyo-expand-drug-discovery-collaboration-in-oncology-36422/#comments</comments>
		<pubDate>Tue, 12 Oct 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Investors]]></category>

		<category><![CDATA[Joint Ventures]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[Massachusetts]]></category>

		<category><![CDATA[October 12]]></category>

		<category><![CDATA[Woburn]]></category>

		<guid isPermaLink="false">http://blog.taragana.com/pr/arqule-and-daiichi-sankyo-expand-drug-discovery-collaboration-in-oncology-36422/</guid>
		<description><![CDATA[WOBURN, Massachusetts, October 12, 2010  - ArQule, Inc. (NASDAQ: ARQL) and Daiichi Sankyo Co., Ltd. (TSE
4568) today announced the expansion of their research, development and
license agreement for the discovery of novel kinase inhibitors in the field
of oncology. This expanded agreement establishes a third therapeutic target,
with an option for a fourth, in the field of .... <a href="http://pr.gaeatimes.com/arqule-and-daiichi-sankyo-expand-drug-discovery-collaboration-in-oncology-36422/">Original article &nbsp;: ArQule and Daiichi Sankyo Expand Drug Discovery Collaboration in Oncology</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/arqule-and-daiichi-sankyo-expand-drug-discovery-collaboration-in-oncology-36422/feed/</wfw:commentRss>
		</item>
		<item>
		<title>New High-Resolution Computer Tomography Data Demonstrates EVISTA(R)&apos;s Effect on Bone Quality in Osteoporotic Patients</title>
		<link>http://pr.gaeatimes.com/new-high-resolution-computer-tomography-data-demonstrates-evistars-effect-on-bone-quality-in-osteoporotic-patients-23062/</link>
		<comments>http://pr.gaeatimes.com/new-high-resolution-computer-tomography-data-demonstrates-evistars-effect-on-bone-quality-in-osteoporotic-patients-23062/#comments</comments>
		<pubDate>Mon, 28 Jun 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi-sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Business]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Medical Equipment]]></category>

		<category><![CDATA[New Products / Services]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[Germany]]></category>

		<category><![CDATA[June 28]]></category>

		<category><![CDATA[Munich]]></category>

		<guid isPermaLink="false">http://blog.taragana.com/pr/new-high-resolution-computer-tomography-data-demonstrates-evistars-effect-on-bone-quality-in-osteoporotic-patients-23062/</guid>
		<description><![CDATA[3D Images Provide New Approach to Monitoring Bone Changes
MUNICH, June 28, 2010  - Interim data from a prospective Investigator Initiated Trial
(IIT) presented today at the ECTS, the 37th European Symposium on Calcified
Tissues, in Glasgow, demonstrates that EVISTA(R) (raloxifene 60mg;
once-daily, distributed in 34 countries by DAIICHI SANKYO), indicated for the
treatment and prevention of osteoporosis in .... Source article &nbsp;: <a href="http://pr.gaeatimes.com/new-high-resolution-computer-tomography-data-demonstrates-evistars-effect-on-bone-quality-in-osteoporotic-patients-23062/">New High-Resolution Computer Tomography Data Demonstrates EVISTA(R)&apos;s Effect on Bone Quality in Osteoporotic Patients</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/new-high-resolution-computer-tomography-data-demonstrates-evistars-effect-on-bone-quality-in-osteoporotic-patients-23062/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Patients with Hypertension at Risk Due to Physician Inertia</title>
		<link>http://pr.gaeatimes.com/patients-with-hypertension-at-risk-due-to-physician-inertia-22559/</link>
		<comments>http://pr.gaeatimes.com/patients-with-hypertension-at-risk-due-to-physician-inertia-22559/#comments</comments>
		<pubDate>Mon, 21 Jun 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Business]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

		<category><![CDATA[Media]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Surveys / Polls / Research]]></category>

		<category><![CDATA[Trade Show]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[June 21]]></category>

		<category><![CDATA[Norway]]></category>

		<category><![CDATA[Oslo]]></category>

		<guid isPermaLink="false">http://blog.taragana.com/pr/patients-with-hypertension-at-risk-due-to-physician-inertia-22559/</guid>
		<description><![CDATA[New Supporting Hypertension Awareness and Research Europe-wide (SHARE) Survey Reports Findings at the 20th Annual Society of the European Society of Hypertension (ESH)

OSLO, June 21, 2010  - Data announced for the first time at ESH suggest that patients
with hypertension are at increased cardiovascular risk due to clinician
inertia, because physicians are failing to treat targets ... <a href="http://pr.gaeatimes.com/patients-with-hypertension-at-risk-due-to-physician-inertia-22559/">Read more : Patients with Hypertension at Risk Due to Physician Inertia</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/patients-with-hypertension-at-risk-due-to-physician-inertia-22559/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Daiichi Sankyo Submits First New Drug Application for Oral Factor Xa Inhibitor, Edoxaban</title>
		<link>http://pr.gaeatimes.com/daiichi-sankyo-submits-first-new-drug-application-for-oral-factor-xa-inhibitor-edoxaban-15619/</link>
		<comments>http://pr.gaeatimes.com/daiichi-sankyo-submits-first-new-drug-application-for-oral-factor-xa-inhibitor-edoxaban-15619/#comments</comments>
		<pubDate>Tue, 06 Apr 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Business]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Health Care / Hospitals]]></category>

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		<category><![CDATA[April 6]]></category>

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		<guid isPermaLink="false">http://blog.taragana.com/pr/daiichi-sankyo-submits-first-new-drug-application-for-oral-factor-xa-inhibitor-edoxaban-15619/</guid>
		<description><![CDATA[Innovative Once-Daily Oral Factor Xa Inhibitor Submitted for Approval in Japan

TOKYO, April 6, 2010  - Daiichi Sankyo Company, Limited announced today that it has
submitted a New Drug Application to the Ministry of Health, Labor and Welfare
in Japan seeking approval of the anticoagulant, edoxaban, for the prevention
of venous thromboembolism (VTE) after major orthopedic surgery.
  ... <a href="http://pr.gaeatimes.com/daiichi-sankyo-submits-first-new-drug-application-for-oral-factor-xa-inhibitor-edoxaban-15619/">Read more : Daiichi Sankyo Submits First New Drug Application for Oral Factor Xa Inhibitor, Edoxaban</a>.]]></description>
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		<title>HOKUSAI VTE - Largest Single Phase III Trial for the Treatment and Prevention of Recurrent VTE Started in Europe</title>
		<link>http://pr.gaeatimes.com/hokusai-vte-largest-single-phase-iii-trial-for-the-treatment-and-prevention-of-recurrent-vte-started-in-europe-13821/</link>
		<comments>http://pr.gaeatimes.com/hokusai-vte-largest-single-phase-iii-trial-for-the-treatment-and-prevention-of-recurrent-vte-started-in-europe-13821/#comments</comments>
		<pubDate>Fri, 26 Feb 2010 05:00:00 +0000</pubDate>
		<dc:creator>Daiichi Sankyo</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

		<category><![CDATA[Health]]></category>

		<category><![CDATA[Pharmaceuticals]]></category>

		<category><![CDATA[Daiichi-Sankyo]]></category>

		<category><![CDATA[February 26]]></category>

		<category><![CDATA[Germany]]></category>

		<category><![CDATA[Japan]]></category>

		<category><![CDATA[Nuremberg]]></category>

		<guid isPermaLink="false">http://blog.taragana.com/pr/hokusai-vte-largest-single-phase-iii-trial-for-the-treatment-and-prevention-of-recurrent-vte-started-in-europe-13821/</guid>
		<description><![CDATA[Potential New Treatment Option for Patients With Venous Thromboembolism (VTE) Offers Effective and Convenient Dosing Regimen

NUREMBERG, Germany, February 26, 2010  - Edoxaban, a direct oral factor Xa inhibitor, is now being
investigated in a second large-scale pivotal phase III trial, HOKUSAI
(pronounced hoek-sigh) VTE. This phase III trial is evaluating the safety and
efficacy of edoxaban in .... Read the original article &nbsp;: <a href="http://pr.gaeatimes.com/hokusai-vte-largest-single-phase-iii-trial-for-the-treatment-and-prevention-of-recurrent-vte-started-in-europe-13821/">HOKUSAI VTE - Largest Single Phase III Trial for the Treatment and Prevention of Recurrent VTE Started in Europe</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/hokusai-vte-largest-single-phase-iii-trial-for-the-treatment-and-prevention-of-recurrent-vte-started-in-europe-13821/feed/</wfw:commentRss>
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		<title>Analysis of Edoxaban Phase II Data Provides Insight Into Reduced Bleeding Events Seen in Once-Daily Dosing</title>
		<link>http://pr.gaeatimes.com/analysis-of-edoxaban-phase-ii-data-provides-insight-into-reduced-bleeding-events-seen-in-once-daily-dosing-4157/</link>
		<comments>http://pr.gaeatimes.com/analysis-of-edoxaban-phase-ii-data-provides-insight-into-reduced-bleeding-events-seen-in-once-daily-dosing-4157/#comments</comments>
		<pubDate>Wed, 15 Jul 2009 05:00:00 +0000</pubDate>
		<dc:creator>Prne</dc:creator>
		
		<category><![CDATA[Business]]></category>

		<category><![CDATA[Clinical Trials / Medical Discoveries]]></category>

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		<category><![CDATA[Bostonedison]]></category>

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		<guid isPermaLink="false">http://blog.taragana.com/pr/analysis-of-edoxaban-phase-ii-data-provides-insight-into-reduced-bleeding-events-seen-in-once-daily-dosing-4157/</guid>
		<description><![CDATA[BOSTON and EDISON, New Jersey - 
&#8211; Pharmacokinetic Analysis of Atrial Fibrillation Study May Explain Bleeding Rate Difference between Once-Daily and Twice-Daily Dosing Regimens with Same Total Exposure of Factor Xa Inhibitor &#8211;

A sub-analysis of a Phase IIb multinational study(1) with edoxaban(2) &#8212; an investigational oral Factor Xa inhibitor - provides insights into why patients  [..] <a href="http://pr.gaeatimes.com/analysis-of-edoxaban-phase-ii-data-provides-insight-into-reduced-bleeding-events-seen-in-once-daily-dosing-4157/">Read the original article: here</a>.]]></description>
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		<item>
		<title>Osteoporosis Drug Heritage Continues Ahead of 10th Anniversary</title>
		<link>http://pr.gaeatimes.com/osteoporosis-drug-heritage-continues-ahead-of-10th-anniversary-2283/</link>
		<comments>http://pr.gaeatimes.com/osteoporosis-drug-heritage-continues-ahead-of-10th-anniversary-2283/#comments</comments>
		<pubDate>Tue, 19 May 2009 05:00:00 +0000</pubDate>
		<dc:creator>Prne</dc:creator>
		
		<category><![CDATA[Biotechnology]]></category>

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		<guid isPermaLink="false">http://blog.taragana.com/pr/osteoporosis-drug-heritage-continues-ahead-of-10th-anniversary-2283/</guid>
		<description><![CDATA[LONDON -  Study Results Demonstrate Patients Continue to Adhere to Treatment With Raloxifene
To view a Vodcast of Professor Peyman Hadji presenting the data click here: 62.193.238.61/blueprinttv/expert/Expert-Opinion.html

To view a Vodcast of a Patient&#8217;s Perspective click here:
62.193.238.61/blueprinttv/expert/The-Patient-Perspetive.html
Data presented today at the 8th European Congress on Menopause (EMAS) demonstrated that the majority of osteoporosis patients treated with .... Source article on Gaea Times at  &nbsp;: <a href="http://pr.gaeatimes.com/osteoporosis-drug-heritage-continues-ahead-of-10th-anniversary-2283/">Osteoporosis Drug Heritage Continues Ahead of 10th Anniversary</a>.]]></description>
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		</item>
		<item>
		<title>EVISTA(R) Improves Patient Compliance in Osteoporosis Management</title>
		<link>http://pr.gaeatimes.com/evistar-improves-patient-compliance-in-osteoporosis-management-2284/</link>
		<comments>http://pr.gaeatimes.com/evistar-improves-patient-compliance-in-osteoporosis-management-2284/#comments</comments>
		<pubDate>Tue, 19 May 2009 05:00:00 +0000</pubDate>
		<dc:creator>Prne</dc:creator>
		
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		<category><![CDATA[Multimedia / Online / Internet]]></category>

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		<category><![CDATA[Daiichi-Sankyo]]></category>

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		<guid isPermaLink="false">http://blog.taragana.com/pr/evistar-improves-patient-compliance-in-osteoporosis-management-2284/</guid>
		<description><![CDATA[LONDON -  Study Results Demonstrate Patients Adhere to Treatment Regimens With EVISTA(R)
To view a Vodcast of Professor Peyman Hadji presenting the data click the following link: 62.193.238.61/blueprinttv/expert/Expert-Opinion.html

To view a Vodcast of a Patient&#8217;s Perspective click the following link: 62.193.238.61/blueprinttv/expert/The-Patient-Perspetive.html
LONDON, May 19 /PRNewswire/ &#8211;
Data presented today at the 8th European Congress on Menopause (EMAS) demonstrated ... <a href="http://pr.gaeatimes.com/evistar-improves-patient-compliance-in-osteoporosis-management-2284/">Read the original article on Gaea Times at  : EVISTA(R) Improves Patient Compliance in Osteoporosis Management</a>.]]></description>
		<wfw:commentRss>http://pr.gaeatimes.com/evistar-improves-patient-compliance-in-osteoporosis-management-2284/feed/</wfw:commentRss>
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