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New FDA-Approved Device For Treatment Of Drug-Resistant Epilepsy Now Offering Hope To Patients In U.S.

From the Wires Jul. 29, 2015 11:00 AM HOUSTON , July 29, 2015 /PRNewswire/ --In just one month following FDA approval of the AspireSR ®... ...

http://in.sys-con.com/node/3389674
Basilea announces that CHMP recommends approval of isavuconazole (CRESEMBA(R)) as a treatment for invasive aspergillosis and mucormycosis in the European Union

GlobeNewswire 2015-07-24BASEL, Switzerland, July 24, 2015 (GLOBE NEWSWIRE) -- Basilea Pharmaceutica Ltd. (SIX: BSLN) announced today that the... ...

http://www.bizwireexpress.com/showstoryGNW.php?storyid=78015
Bristol-Myers Squibb's Nivolumab BMS receives EU approval to treat metastatic squamous NSCLC

The European Commission has approved Bristol-Myers Squibb Company's Nivolumab BMS for the treatment of locally advanced or metastatic squamous (SQ)... ...

http://www.pharmabiz.com/NewsDetails.aspx?aid=89526&sid=2
Baxalta's BAX 855 Pivotal Data Published in Blood Shows Potential to Provide Strong Bleed Prevention with Twice..

/PRNewswire/ -- Nektar Therapeutics (Nasdaq: NKTR) reported that partner Baxalta Incorporated, a global biopharmaceutical leader dedicated to... ...

http://in.advfn.com/p.php?pid=nmona&article=67750847
IMBRUVICA® (ibrutinib) Now Approved to Treat Waldenstrom's Macroglobulinemia in Europe

/PRNewswire/ --TodayAbbVie (NYSE: ABBV) announced the European Commission (EC) granted marketing authorization for IMBRUVICA ® (ibrutinib) as the... ...

http://in.advfn.com/p.php?pid=nmona&article=67651696

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