News articles for Daiichi Sankyo, Inc.:
Friday, October 21, 2011
Thursday, September 8, 2011
Wednesday, August 17, 2011
FDA Approval of Zelboraf(TM) (vemurafenib) Establishes Oncology Foothold in US for Daiichi Sankyo
PARSIPPANY, N.J., Aug. 17, 2011 /PRNewswire/ -- With the US Food and Drug Administration (FDA) approval today of Zelboraf(TM) (vemurafenib), a first-in-class personalized treatment for patients with unresectable (inoperable) or metastatic melanoma with a BRAF V600E mutation as detected by an FDA-approved test, Daiichi Sankyo prepares to enter the US ...
read moreDaiichi Sankyo, Inc. Appoints Executive Vice President of Drug Development for the Americas
PARSIPPANY, N.J., Aug. 17, 2011 /PRNewswire/ -- Daiichi Sankyo, Inc. announced that Mahmoud Ghazzi, MD, PhD has joined Daiichi Sankyo Pharma Development (DSPD) as its new executive vice president of drug development for the Americas region.
DSPD, headquartered in Edison, NJ, is responsible for the regional delivery of global clinical ...
read more Monday, May 3, 2010
Saturday, May 1, 2010
Wednesday, May 13, 2009
AZOR(R) Receives FDA Approval as First-Line Treatment for High Blood Pressure
PARSIPPANY, NJ -- (Marketwire) -- 05/13/09 -- Daiichi Sankyo, Inc. today announced that
the United States Food and Drug Administration (FDA) has approved the
combination treatment AZOR® (amlodipine and olmesartan medoxomil) as
initial or 'first-line' therapy in patients likely to need multiple
antihypertensive agents to achieve their blood pressure (BP) goals. The FDA
approval ...
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