Astellas Pharma

Astellas and XenoPort Announce Submission of a New Drug Application in Japan Requesting PMDA...

Astellas Pharma Inc. and XenoPort, Inc. (NASDAQ:XNPT) today announced that a new drug application (NDA) has been filed with the Pharmaceuticals and Medical Device Agency (PMDA) in Japan for ASP8825 (gabapentin enacarbil), also...

powered by

Nikkei set to rise after U.S. shares rally (at Reuters)

TOKYO, Nov 17 (Reuters) - Japan's Nikkei stock average is likely to rise on Tuesday after U.S. shares surged due to comments by Federal Reserve Chairman Ben Bernanke that reinforced expectations that interest rates would stay...

powered by

NeurogesX Receives FDA Approval of Qutenza(TM) (capsaicin) 8% Patch for Treatment of Postherpetic...

SAN MATEO, Calif., Nov. 16 /PRNewswire-FirstCall/ -- NeurogesX, Inc. announced today that the U.S. Food and Drug Administration (FDA) has approved Qutenza(TM) (capsaicin) 8% patch, the first and only product containing...

powered by

Maxygen starts buyback offer for 6.6M shares (AP)

REDWOOD CITY, Calif. (AP) -- Biotechnology company Maxygen Inc. said Friday it is starting a tender offer to buy back 6.6 million shares of its stock, or about a sixth of its outstanding shares. Maxygen said it will pay between...

powered by

Medivation to Present at Lazard Capital Markets Sixth Annual Healthcare Conference

SAN FRANCISCO, Nov. 11 /PRNewswire-FirstCall/ -- Medivation, Inc. today announced that David Hung, M.D., president and chief executive officer, will present at Lazard Capital Markets Sixth Annual Healthcare conference on...

powered by

Ironwood and Astellas Announce Japan Licensing Agreement for Linaclotide

Ironwood Pharmaceuticals, Inc. and Astellas Pharma Inc. today announced that they have entered into an agreement providing Astellas exclusive rights to develop and commercialize the investigational compound linaclotide in...

powered by

CORRECTING and REPLACING GlaxoSmithKline and XenoPort Announce Extension of GSK1838262 (XP13512)...

In BW 5972 issued November 6, 2009: First graph, second sentence of release (dated November 6, 2009) should read: The NDA currently under review by the FDA is for the treatment of moderate-to-severe primary Restless Legs...

powered by

Astellas Pharma Europe Announces Save the Children as a Winner of the Changing Tomorrow 2009 Awards

STAINES, England, November 10 /PRNewswire/ -- Astellas Pharma Europe, the European subsidiary of Tokyo-based Astellas Pharma Inc, one of the world's top 20 pharmaceutical companies, can today announce details of an Astellas...

powered by

Theravance, Inc. (THRX) and Astellas Pharma Inc. Announce the Commercial Launch of VIBATIV(TM)...

Theravance, Inc. (NASDAQ: THRX) and Astellas Pharma US, Inc. announced today the commercial launch of VIBATIVT (telavancin) in the United States. On September 11, 2009, the U.S. Food and Drug Administration (FDA) approved...

powered by

GlaxoSmithKline and XenoPort Announce Extension of GSK1838262 (XP13512) FDA Review Date to...

.bwcellpaddingleft0 {padding-left: 0.0px} .bwcellparagraphmargin {margin-bottom: 0px; margin-top: 0px} .bwtablebottommargin {margin-bottom: 10.0px} .bwtextalignleft {text-align: left} .bwunderlinestyle {text-decoration: ...

powered by
1 2 3 4 5 next »