<rss version="2.0"><channel><title>BioSpace.com News</title><link>http://www.biospace.com</link><generator>BioSpace RSS Generator</generator><lastBuildDate>Tue, 18 Jun 2013 23:48:33 GMT</lastBuildDate><ttl>20</ttl><image><url>http://rss.biospace.com/images/BSPLogo.gif</url><title>BioSpace.com</title><link>http://www.BioSpace.com/news.aspx?SectionId=1</link></image><copyright>Copyright (C) 2011</copyright><item><title>Ipsen Release: "PRIMARYS" Study Investigators Observed Clinically Relevant Results in an Investigational Phase III Study With Somatuline&amp;#0174; Autogel&amp;#0174; 120 mg in Patients With Acromegaly  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.b30484b92e958b11adda3242e6908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130617006399&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;PARIS--(BUSINESS WIRE)--Ipsen (Euronext: IPN; ADR: IPSEY) today announced the results of an international phase IIIB study, PRIMARYS, assessing an investigational use of Somatuline Autogel (lanreotide) 1...</description><pubDate>Tue, 18 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Orexo AB Release: First Patient Dosed in New Phase III Study Targeted Towards a Future Clinical Indication Expansion for Zubsolv  </title><link>http://www.globenewswire.com/news-release/2013/06/17/554326/0/en/First-patient-dosed-in-new-phase-III-study-targeted-towards-a-future-clinical-indication-expansion-for-Zubsolv.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Uppsala, Sweden  June 17, 2013 - Orexo AB announces today that the firstpatient has been dosed with Zubsolv in a phase III study for a new clinicalindication for Zubsolv.&lt;br&gt;&lt;br&gt;Help employers find...</description><pubDate>Mon, 17 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Orexo AB: First Patient Dosed in New Phase III Study Targeted Towards a Future Clinical Indication Expansion for Zubsolv  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.ab520ce17e34ab71ff00d635c0908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130616005101&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;UPPSALA, Sweden--(BUSINESS WIRE)--Regulatory News: Orexo AB (STO:ORX) announces today that the first patient has been dosed with Zubsolv in a phase III study for a new clinical indication for Zubsolv. Currently...</description><pubDate>Mon, 17 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Incyte Corporation Drug Jakafi&amp;#0174; (ruxolitinib) Improved Overall Survival in Phase III Trial of Patients With Myelofibrosis
  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.b30484b92e958b11adda3242e6908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130615005030&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;STOCKHOLM--(BUSINESS WIRE)--Incyte Corporation (Nasdaq: INCY) today announced results from two ongoing clinical trials of Jakafi (ruxolitinib), an oral JAK1 and JAK2 inhibitor that is FDA-approved for the treatment...</description><pubDate>Mon, 17 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Immunomedics, Inc. Presents Epratuzumab's Mechanism of Action in Systemic Lupus Erythematosus  </title><link>http://www.globenewswire.com/news-release/2013/06/13/553934/10036120/en/Immunomedics-Presents-Epratuzumab-s-Mechanism-of-Action-in-Systemic-Lupus-Erythematosus.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;MADRID, Spain, June 13, 2013 (GLOBE NEWSWIRE) -- Immunomedics, Inc. (Nasdaq: IMMU), a biopharmaceutical company primarily focused on the development of monoclonal antibody-based products for the targeted treatment...</description><pubDate>Thu, 13 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Ferrer Internacional Successfully Completes a Phase III Clinical Trial in Adult and Paediatric Patients With Impetigo for Novel Antibacterial Compound Ozenoxacin  </title><link>http://www.biospace.com/news_story.aspx?StoryID=299819&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Barcelona, Spain, June 5, 2013 - Ferrer, a privately-held Spanish pharmaceutical company with full vertical integration from R&amp;D to distribution, announces today that it has successfully completed a phase III...</description><pubDate>Wed, 12 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Celgene International S??rl Release: Signs and Symptoms of Psoriatic Arthritis Significantly Improved in Patients Receiving Long-Term Oral Apremilast Treatment in Phase III Study (PALACE-1)  </title><link>http://www.biospace.com/news_story.aspx?StoryID=299831&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;BOUDRY, Switzerland  (June 12, 2013) Celgene International Srl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ: CELG), today announced 52-week results from PALACE 1, the Companys first phase III...</description><pubDate>Wed, 12 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Janssen Biotech Inc. Release: Five-Year SIMPONI Data Reported In Treatment of Signs and Symptoms of Moderately to Severely Active Rheumatoid Arthritis  </title><link>http://www.biospace.com/news_story.aspx?StoryID=299873&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;div class"xn-content"&gt;&lt;p&gt;&lt;span class"xn-location"&gt;MADRID&lt;/span&gt;, &lt;span class"xn-chron"&gt;June 12, 2013&lt;/span&gt; /PRNewswire/ --Janssen Biotech, Inc. announced today new five-year data from three pivotal Phase...</description><pubDate>Wed, 12 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Boehringer Ingelheim Corporation's Investigational Faldaprevir+ Achieved Viral Cure in 88% of Treatment-Naive Hepatitis C Patients in Asia  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.b30484b92e958b11adda3242e6908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130608005008&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;INGELHEIM, Germany--(BUSINESS WIRE)--New findings presented today during the APASL Liver Week in Singapore, highlighted the efficacy and safety of faldaprevir plus pegylated interferon and ribavirin (PegIFN...</description><pubDate>Mon, 10 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>AstraZeneca PLC Scraps Rigel Pharmaceuticals, Inc. Arthritis Pill in New R&amp;D Blow, to Write Off $140 Million Charge  </title><link>online.wsj.com/article/BT-CO-20130604-700544.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;font size"3"&gt;&lt;b&gt;AstraZeneca announces top-line results from Phase III OSKIRA Trials of FOSTAMATINIB and decision not to proceed with regulatory filings&lt;/font&gt;&lt;/b&gt;&lt;br&gt;&lt;br&gt;June 04, 2013 -- Rights to the...</description><pubDate>Thu, 06 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Medivir AB Release: Primary Efficacy and Safety Data From Four Phase III Japanese Studies of Simeprevir Presented at  </title><link>http://www.globenewswire.com/news-release/2013/06/06/552505/0/en/Primary-efficacy-and-safety-data-from-four-phase-III-Japanese-studies-of-Simeprevir-presented-at-The-Japan-Society-of-Hepatology.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Stockholm, Sweden  Medivir AB (OMX: MVIR) reports that its partner JanssenPharmaceutical R&amp;D Ireland (Janssen) today announced primary efficacy and safetyresults from four Japanese phase III clinical studies...</description><pubDate>Thu, 06 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Boehringer Ingelheim Corporation Release: LUME-Lung 1: Nintedanib* Plus Chemotherapy Extends the Life of Lung Cancer Patients With Adenocarcinoma  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.b30484b92e958b11adda3242e6908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130603005747&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;INGELHEIM, Germany--(BUSINESS WIRE)--The LUME-Lung 1 Phase III clinical trial results showed that the novel investigational compound nintedanib*, an oral triple angiokinase inhibitor, extended life by 2.3 months...</description><pubDate>Mon, 03 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Takeda Pharmaceutical Co. Ltd. Release: American Society of Clinical Oncology Presentation Highlights Results of Single Agent oral MLN9708 in Heavily Pretreated Patients with Relapsed and/or Refractory Multiple Myeloma  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130603006028&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;CHICAGO &amp; OSAKA, Japan--(BUSINESS WIRE)--Takeda Pharmaceutical Company Limited (TSE:4502) today reported results from a Phase 1 study evaluating the safety, tolerability, and maximum tolerated dose (MTD) of...</description><pubDate>Mon, 03 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Celgene International S??rl Release: Analyses of MPACT Trial Evaluating ABRAXANE?? Combination Therapy for the Treatment of Advanced Pancreatic Cancer Presented at American Society of Clinical Oncology 2013  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130603005436&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;BOUDRY, Switzerland--(BUSINESS WIRE)--Celgene International Srl, a subsidiary of Celgene Corporation (NASDAQ: CELG), announced several analyses of a phase III clinical trial of ABRAXANE (paclitaxel protein...</description><pubDate>Mon, 03 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>Celgene International S??rl Release: Updated Studies Evaluating POMALYST&amp;#0174; (pomalidomide) In Previously Treated Multiple Myeloma Patients Presented at American Society of Clinical Oncology  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130603005918&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;BOUDRY, Switzerland--(BUSINESS WIRE)--Celgene International Srl, a wholly-owned subsidiary of Celgene Corporation (NASDAQ: CELG), today announced updated data from MM-003, the Companys phase III international...</description><pubDate>Mon, 03 Jun 2013 12:00:00 AM GMT</pubDate></item><item><title>FDA Designates Alexion Pharmaceuticals Inc.'s Product for Rare Disease as "Breakthrough Therapy"  </title><link>http://www.biospace.com/news_story.aspx?StoryID=298003&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;font size"3"&gt;&lt;b&gt; &lt;/font&gt;&lt;/b&gt;&lt;br&gt;&lt;br&gt;LAUSANNE, Switzerland--(BUSINESS WIRE)--Alexion Pharma International Srl, a subsidiary of Alexion Pharmaceuticals, Inc. (Nasdaq: ALXN), today announced that the U...</description><pubDate>Thu, 30 May 2013 12:00:00 AM GMT</pubDate></item><item><title>GlaxoSmithKline, Genmab A/S Say Combo Boosts PFS in P3 Leukemia Study  </title><link>http://www.biospace.com/news_story.aspx?StoryID=298301&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;font size"3"&gt;&lt;b&gt;GSK and Genmab Announce Positive Top-Line Results From Pivotal Study of ARZERRA(R) (ofatumumab) Combined With Chlorambucil in Previously Untreated Chronic Lymphocytic Leukemia&lt;/font&gt;&lt;/b&gt;...</description><pubDate>Thu, 30 May 2013 12:00:00 AM GMT</pubDate></item><item><title>&lt;b&gt;Beijing Vigoo Biological&lt;/b&gt; Says EV71 Vaccine Passes Phase III Test  </title><link>http://www.chinabiotoday.com/articles/20130529_1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;by Richard Daverman, PhD&lt;/p&gt;&lt;p&gt;May 29, 2013 -- Beijing Vigoo Biological, a vaccine-focused subsidiary of China National Biotec Group, reported that its Enterovirus 71 vaccine was effective in up to 90% of...</description><pubDate>Thu, 30 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Amarin Corporation PLC Announces Additional Effects of Vascepa&amp;#0174; on Lipoprotein Particle Concentration From the ANCHOR Study Presented at the Annual Scientific Sessions  </title><link>http://www.globenewswire.com/news-release/2013/05/30/550727/10034456/en/Amarin-Announces-Additional-Effects-of-Vascepa-R-on-Lipoprotein-Particle-Concentration-From-the-ANCHOR-Study-Presented-at-the-National-Lipid-Association-2013-Annual-Scientific-Sess.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;BEDMINSTER, N.J. and DUBLIN, Ireland, May 30, 2013 (GLOBE NEWSWIRE) -- Amarin Corporation plc (Nasdaq:AMRN), a biopharmaceutical company focused on the commercialization and development of therapeutics to improve...</description><pubDate>Thu, 30 May 2013 12:00:00 AM GMT</pubDate></item><item><title>NeuroVive Pharmaceutical AB: European Phase III Study Approaches Its Final Stage  </title><link>http://www.globenewswire.com/news-release/2013/05/29/550325/0/en/NeuroVive-European-phase-III-study-approaches-its-final-stage.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;NeuroVive Pharmaceutical AB (publ), a leading mitochondrial medicine company,announces that the ongoing international multicenter phase III study on thecompanys drug candidate CicloMulsion (the CIRCUS...</description><pubDate>Wed, 29 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Novo Nordisk A/S Says Obesity Drug Trial Confirms Weight Loss  </title><link>http://www.biospace.com/news_story.aspx?StoryID=297844&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;BAGSVAERD, Denmark I 23 May 2013 I Novo Nordisk today announced the headline results from a 56-week double-blind phase 3a clinical trial investigating the potential of liraglutide to induce and maintain weight...</description><pubDate>Tue, 28 May 2013 12:00:00 AM GMT</pubDate></item><item><title>SALVAT Completes Enrollment of Phase III Study for a New Combination in Acute Otitis Media in Pediatric Patients With Tympanostomy Tubes (AOMT)  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130528005288&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;BARCELONA, Spain--(BUSINESS WIRE)--SALVAT announced that clinical trial enrollment has completed for the Phase III study evaluating the efficacy and safety of a new otic solution containing Ciprofloxacin and...</description><pubDate>Tue, 28 May 2013 12:00:00 AM GMT</pubDate></item><item><title>TauRx Therapeutics Release: First UK Patients Enroll in Phase 3 Clinical Trials of LMTX&amp;#0153; for Alzheimer's Disease  </title><link>http://www.biospace.com/news_story.aspx?StoryID=297810&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Aberdeen, United Kingdom, 22 May 2013  Coinciding with Dementia Awareness Week in the UK, TauRx Therapeutics Ltd announced that the first of more than 100 UK patients have enrolled in the global Phase 3 clinical...</description><pubDate>Thu, 23 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Bayer HealthCare Says Lung Drug Shows Promise in Prolonged Trial  </title><link>http://www.biospace.com/news_story.aspx?StoryID=297364&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;font size"3"&gt;&lt;b&gt;Bayer Presents Positive Interim Results from Long-term Extension Study PATENT-2 with Riociguat&lt;/font&gt;&lt;/b&gt;&lt;br&gt;&lt;br&gt;Berlin, May 20, 2013  Bayer HealthCare today announced positive data from...</description><pubDate>Wed, 22 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Medivir AB Release: Primary Efficacy and Safety Findings From Phase III Study of Simeprevir in Treatment-Experienced Patients Demonstrate Sustained Virologic Response  </title><link>http://www.globenewswire.com/news-release/2013/05/21/548678/0/en/Primary-efficacy-and-safety-findings-from-phase-III-study-of-Simeprevir-in-treatment-experienced-patients-demonstrate-sustained-virologic-response.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Stockholm, Sweden  Medivir AB (OMX: MVIR) reports that its partner Janssen R&amp;DIreland (Janssen) today announced primary efficacy and safety results from theglobal phase III PROMISE study. Results demonstrated...</description><pubDate>Tue, 21 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Vectura Group plc Release: New Data Presented at the American Thoracic Society Meeting Highlights Strength of Once-Daily COPD Portfolio in Improving Lung Function, Shortness of Breath and Reducing Rate of Exacerbations  </title><link>http://www.biospace.com/news_story.aspx?StoryID=297430&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Chippenham, UK  21 May 2013: Vectura Group plc (LSE: VEC) (Vectura), confirms theinformation released today by Novartis announcing that new data from the chronic obstructivepulmonary disease (COPD) portfolio...</description><pubDate>Tue, 21 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Genentech Cancer Antibody, Son of Rituxan, Nails Pivotal Study  </title><link /><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;b&gt;Roche's obinutuzumab (GA101) significantly reduced the risk of disease progression or death in people with one of the most common forms of blood cancer&lt;/b&gt;&lt;br&gt;&lt;br&gt;Basel, 16 May 2013 -- Roche (SIX: RO...</description><pubDate>Mon, 20 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Sanofi (France) Plans to File JAK2 Inhibitor After Positive Phase III  </title><link>http://www.biospace.com/news_story.aspx?StoryID=297084&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;font size"3"&gt;&lt;b&gt;Sanofi Reports Positive Topline Results from Pivotal Phase III JAKARTA Study for JAK2 Inhibitor in Myelofibrosis&lt;/font&gt;&lt;/b&gt;&lt;br&gt;&lt;br&gt;Paris, France - May 17, 2013- Sanofi (EURONEXT: SAN and...</description><pubDate>Mon, 20 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Veloxis Pharmaceuticals A/S Release: Final STRATO Clinical Study Data Demonstrates Potential for LCP-TacroTM to Improve Tacrolimus-Induced Tremors  </title><link>http://www.globenewswire.com/news-release/2013/05/20/548304/0/en/Final-STRATO-Clinical-Study-Data-Demonstrates-Potential-for-LCP-TacroTM-to-Improve-Tacrolimus-Induced-Tremors.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Veloxis Pharmaceuticals A/S (OMX: VELO) today announced that data from the STRATO study demonstrates the potential for LCP-Tacro to improve tacrolimus-induced tremors in stable kidney transplant patients. ...</description><pubDate>Mon, 20 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Lundbeck Inc. Release: Vortioxetine Clinical Phase III Data Show Significant Improvement in Symptoms of Major Depression  </title><link>http://www.globenewswire.com/news-release/2013/05/18/548245/0/en/Vortioxetine-clinical-phase-III-data-show-significant-improvement-in-symptoms-of-major-depression.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Valby, Denmark, 18 May 2013 - H. Lundbeck A/S (Lundbeck) and partner Takeda Pharmaceutical Company Limited (Takeda) today announced that the companies will be presenting new data on four pivotal studies on vortioxetine...</description><pubDate>Mon, 20 May 2013 12:00:00 AM GMT</pubDate></item><item><title>AB Science: Launch of a Phase 3 Clinical Trial in Alzheimer's Disease  </title><link>http://www.biospace.com/news_story.aspx?StoryID=297310&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;div id"releaseBody"&gt;&lt;p&gt;PARIS--(Marketwired - May       20, 2013) -  &lt;p&gt;&lt;br&gt;&lt;b&gt;Launch of a phase 3 clinical trial in the treatment of Alzheimer's disease with masitinib&lt;/b&gt; &lt;p&gt;&lt;b&gt;First patients recruited...</description><pubDate>Mon, 20 May 2013 12:00:00 AM GMT</pubDate></item><item><title>AstraZeneca PLC Advances Three Cancer Drugs Into Late-Stage Trials  </title><link>http://www.thepharmaletter.com/file/122173/astrazeneca-plans-to-move-three-cancer-drug-candidates-into-ph-iii.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;AstraZeneca Plc (AZN) will move three experimental cancer treatments into late-stage development as generic competition for its best-selling drugs intensifies. The U.K.s second-biggest drugmaker is advancing...</description><pubDate>Fri, 17 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Novo Nordisk A/S Reports Positive Results From First Phase 3 Trial With Long-Acting Factor IX for Treatment of Hemophilia B  </title><link>http://www.biospace.com/news_story.aspx?StoryID=297156&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;div id"releaseBody"&gt;&lt;p&gt;BAGSVAERD, DENMARK--(Marketwired - May       17, 2013) -   Novo Nordisk today announced thecompletion of paradigm&amp;#8482; 2, the first phase 3 trial with a long-actingFIX derivative...</description><pubDate>Fri, 17 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Roche Banks on New Drug Data to Defend Cancer Business  </title><link>http://www.reuters.com/article/2013/05/15/health-cancer-roche-idUSL6N0DV2P220130515</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;ZURICH, May 15 (Reuters) - Swiss drugmaker Roche hopes data published this week will show it has a viable follow-on product to help fend off cheaper competition for its best-selling cancer drug, which loses...</description><pubDate>Thu, 16 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Sanofi (France) and Regeneron Pharmaceuticals, Inc. Announce Patient Enrollment in Two Phase 3 Trials with Sarilumab in Rheumatoid Arthritis (RA)  </title><link>http://www.biospace.com/news_story.aspx?StoryID=296756&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt; &lt;div class"xn-content"&gt;&lt;p&gt;&lt;span class"xn-location"&gt;PARIS&lt;/span&gt; and &lt;span class"xn-location"&gt;TARRYTOWN, N.Y.&lt;/span&gt;, &lt;span class"xn-chron"&gt;May 15, 2013&lt;/span&gt; /PRNewswire/ -- Sanofi (EURONEXT: SAN and...</description><pubDate>Wed, 15 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Medivir AB Release: FDA Grants Priority Review to Simeprevir for Combination Treatment of Genotype 1 Chronic Hepatitis C  </title><link>http://www.globenewswire.com/news-release/2013/05/13/546520/0/en/U-S-FDA-grants-priority-review-to-Simeprevir-for-combination-treatment-of-genotype-1-chronic-hepatitis-C.html</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;Stockholm, Sweden  Medivir AB (OMX: MVIR) today announces that the U.S. Foodand Drug Administration (FDA) has granted Priority Review to the New DrugApplication (NDA) by Janssen for simeprevir (TMC435...</description><pubDate>Mon, 13 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Medivir AB: FDA Grants Priority Review to Simeprevir for Combination Treatment of Genotype 1 Chronic Hepatitis C  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130513005818&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;STOCKHOLM--(BUSINESS WIRE)--Regulatory News: Medivir AB (STO:MVIR-B) today announces that the U.S. Food and Drug Administration (FDA) has granted Priority Review to the New Drug Application (NDA) by Janssen...</description><pubDate>Mon, 13 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Actelion Ltd. Gets Go-Ahead to Continue New Drug Trial  </title><link>http://www.biospace.com/news_story.aspx?StoryID=295796&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;(Thomson Reuters ONE via COMTEX) -- Actelion Pharmaceuticals Ltd / Actelion provides update on Phase III GRIPHON study with selexipag in pulmonary arterial hypertension - Study continues . Processed and transmitted...</description><pubDate>Wed, 08 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Celgene Corporation Release: Apremilast Achieves Statistical Significance for the Primary and Major Secondary Endpoints in Fourth Pivotal Phase III Study (PALACE 4) of Patients With Psoriatic Arthritis  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.b30484b92e958b11adda3242e6908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130506006296&amp;newsLang=en</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;BOUDRY, Switzerland--(BUSINESS WIRE)--Celgene International Srl, a subsidiary of Celgene Corporation (NASDAQ: CELG) today announced that statistical significance was achieved for the primary endpoint of ACR...</description><pubDate>Tue, 07 May 2013 12:00:00 AM GMT</pubDate></item><item><title>Basilea Pharmaceutica Reports Presentation of New Data on Anti-Infective Drug Candidates Addressing Drug Resistance  </title><link>http://www.biospace.com/news_story.aspx?StoryID=294727&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;&lt;div id"releaseBody"&gt;&lt;p&gt;BASEL, SWITZERLAND--(Marketwired - April     29, 2013) -   Basilea Pharmaceutica AG /Basilea reports presentation of new data on anti-infective drug candidatesaddressing drug...</description><pubDate>Mon, 29 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>Active Biotech AB and Ipsen Update the Analysis Plan for the 10TASQ10 Trial Evaluating Tasquinimod in the Treatment of Prostate Cancer  </title><link>http://www.biospace.com/news_story.aspx?StoryID=294424&amp;full=1</link><description>&lt;div id"releaseBody"&gt;&lt;p&gt;LUND, SWEDEN and PARIS--(Marketwired - April     25, 2013) -  &lt;p&gt;&lt;br&gt;  * Primary PFS analysis now expected at the same time as first interimoverall    survival analysis in 2014&lt;p&gt;Active Biotech (NASDAQ OMXNORDIC: ACTI) and Ipsen (Euronext: IPN; ADR: IPSEY) today announced thatthecompanies have updated the analysis plan for the 10TASQ10 trial, a globalPhase...</description><pubDate>Thu, 25 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>Data From Phase 3 Studies of Gilead Sciences, Inc.'s Sofosbuvir for Hepatitis C in the Forefront  </title><link>http://www.biospace.com/news_story.aspx?StoryID=294092&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;sourcenews-signup"&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;AMSTERDAM--(BUSINESS WIRE)--April 23, 2013-- Gilead Sciences, Inc. (Nasdaq: GILD) today announced that detailed results from four Phase 3 clinical trials (NEUTRINO, FISSION, POSITRON and FUSION) evaluating...</description><pubDate>Tue, 23 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>Astellas Pharma Inc., GlaxoSmithKline Vie to Make "High Altitude" Anemia Pill  </title><link>http://www.reuters.com/article/2013/04/19/us-anaemia-pill-idUSBRE93I0GH20130419</link><description>Japan's Astellas Pharma and Britain's GlaxoSmithKline are competing to develop a new kind of medicine that boosts production of red blood cells by making the body think it is at high altitude. Their experimental drugs - both given as pills - could create a major new market in treating anemia and other serious conditions, including circulatory problems and wound damage. They may also attract unscrupulous...</description><pubDate>Mon, 22 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>SCM Pharma Limited  Supports Clinical Scale-Up for Varisolve&amp;#0174;  </title><link>http://www.biospace.com/news_story.aspx?StoryID=293961&amp;full=1</link><description>Staying up-to-date has never been simpler.  Sign up for the &lt;a href"http://www.biospace.com/enewsletter.aspx?typeseo-article&amp;source"news-signup""&gt;free GenePool newsletter&lt;/a&gt; today!&lt;br&gt;&lt;br&gt;April 2013 -- SCM Pharma will assist BTG in preparation for the commercial launch of Varisolve (polidocanol endovenous microfoam (PEM)), after providing clinical development consultancy for the product...</description><pubDate>Mon, 22 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>Teva Pharmaceutical Industries Limited Presented New Data From Phase III Clinical Trial of Milprosa&amp;#0153; (Progesterone) Vaginal Ring at the 61st Annual Meeting of the  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.b30484b92e958b11adda3242e6908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130417005827&amp;newsLang=en</link><description>Teva Pharmaceutical Industries Ltd. (NYSE: TEVA) today presented data from a sub-analysis of a Phase III clinical trial of Milprosa (progesterone) vaginal ring, an investigational, once-weekly therapy for luteal phase support in women undergoing in vitro fertilization (IVF). The results were presented at the 61st Annual Meeting of the Pacific Coast Reproductive Society (PCRS).</description><pubDate>Wed, 17 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>Forest Laboratories, Inc. and Almirall Report Positive COPD Drug Data  </title><link>http://www.biospace.com/news_story.aspx?StoryID=293327&amp;full=1</link><description>BARCELONA &amp; NEW YORK--(BUSINESS WIRE)-- Almirall, S.A. (ALM:MC) and Forest Laboratories, Inc. (FRX) today announced positive topline results from a six month pivotal phase III clinical trial evaluating the efficacy and safety of fixed dose combinations of aclidinium bromide, (LAMA) and formoterol fumarate (LABA) delivered by Almiralls inhaler Genuair (Pressair in the USA).&lt;/p&gt;&lt;p&gt;Both combinations...</description><pubDate>Tue, 16 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>InDex Pharmaceuticals AB Completes Patient Recruitment in P3 Ulcerative Colitis Study With Kappaproct  </title><link>http://www.biospace.com/news_story.aspx?StoryID=292712&amp;full=1</link><description>April 8, 2013 -- InDex Pharmaceuticals, a Swedish biopharmaceutical company, has completed patient enrollment for its phase III COLLECT study of Kappaproct. The multinational, randomized, double-blind, placebo-controlled study reached the recruitment goal of 120 patients with treatment-refractory ulcerative colitis (UC). InDex is expecting final study results in mid-2014.&lt;/p&gt;&lt;p&gt;The phase III trial...</description><pubDate>Mon, 08 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>Medivation, Inc. and Astellas Pharma Inc. Provide Update on PREVAIL  </title><link>http://www.biospace.com/news_story.aspx?StoryID=291964&amp;full=1</link><description>&lt;div id"releaseBody"&gt;&lt;p&gt;SAN FRANCISCO, CA and TOKYO--(Marketwire - April     01, 2013) -   Medivation, Inc. (NASDAQ: &lt;a href"http://www.marketwire.com/mw/stock.jsp?TickerMDVN"&gt;MDVN&lt;/a&gt;) and Astellas Pharma Inc. (TSE: 4503) today announced that the companies have established an updated interim analysis plan for the PREVAIL trial, a global Phase 3 clinical trial evaluating XTANDI&amp;#174; (enzalutamide...</description><pubDate>Mon, 01 Apr 2013 12:00:00 AM GMT</pubDate></item><item><title>Sanofi (France)'s Lemtrada MS Drug Effective in Extension Trial  </title><link /><description>CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Genzyme, a Sanofi Company (EURONEXT: SAN and NYSE: SNY), announced today interim results from the first year of the extension study of LEMTRADA (alemtuzumab), being developed for the treatment for multiple sclerosis (MS).&lt;/p&gt;&lt;p&gt;In this analysis of the first year of the extension study, relapse rates and sustained accumulation of disability remained low among...</description><pubDate>Fri, 22 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Teva Pharmaceutical Industries Limited and Active Biotech AB See Positive Results From MS Study  </title><link>http://www.biospace.com/news_story.aspx?StoryID=291180&amp;full=1</link><description>JERUSALEM &amp; LUND, Sweden--(BUSINESS WIRE)-- Teva Pharmaceutical Industries Ltd. (TEVA) and Active Biotech (NASDAQ OMX NORDIC: ACTI) announced today top-line results from the open-label extension of the Phase III ALLEGRO study that assessed the progression of disability and safety of oral laquinimod in early versus delayed-start relapsing-remitting multiple sclerosis (RRMS) patients. The study compared...</description><pubDate>Thu, 21 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Adocia Announces Its Phase III Development Program for the Treatment of Diabetic Foot Ulcer  </title><link>http://www.biospace.com/news_story.aspx?StoryID=291135&amp;full=1</link><description>Lyon, France, March 19, 2013 - Adocia (NYSE Euronext Paris: FR0011184241 - ADOC), a biotechnology company specialized in the development of best-in-class medicines from already approved therapeutic proteins announces today the  phase III development program of its product, BioChaperone(R) PDGF-BB for the treatment of diabetic foot ulcer (DFU). The European Medicines Agency (EMA) issued positive scientific...</description><pubDate>Wed, 20 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Novo Nordisk A/S Pleased With Obesity Trial Results  </title><link>http://www.biospace.com/news_story.aspx?StoryID=290718&amp;full=1</link><description>&lt;div id"releaseBody"&gt;&lt;p&gt;BAGSVAERD, DENMARK--(Marketwire - March     18, 2013) -  &lt;p&gt;&lt;br&gt;Company announcement No 19 / 2013:&lt;p&gt;&lt;a href"http://hugin.info/2013/R/1685937/552525.pdf"&gt;http://hugin.info/2013/R/1685937/552525.pdf&lt;/a&gt;&lt;p&gt;This announcement is distributed by Thomson Reuters on behalf ofThomson Reuters clients. The owner of this announcement warrants that:&lt;p&gt;(i) the releases...</description><pubDate>Tue, 19 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>R-Tech Ueno: Start of the Patient Enrollment of a Phase 3 Clinical Study of Unoprostone (Development Code UF-021) Ophthalmic Solution for the Treatment of Retinitis Pigmentosa  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.ab520ce17e34ab71ff00d635c0908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130317005084&amp;newsLang=en</link><description>TOKYO--(BUSINESS WIRE)--R-Tech Ueno (JASDAQ:4573) is pleased to announce the start of the patient enrollment of a Phase 3 clinical study with Unoprostone(note 1) (development code UF-021) ophthalmic solution that are being developed in our company for the treatment of retinitis pigmentosa(note 2). The Phase 3 clinical study with UF-021 ophthalmic solution for treatment of retinitis pigmentosa (ClinicalTrials...</description><pubDate>Mon, 18 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>AOP Orphan Pharmaceuticals AG Release: Essential Thrombocythemia (ET) ??? Convincing Data of ANAHYDRET Study Now Published  </title><link>http://www.biospace.com/news_story.aspx?StoryID=290842&amp;full=1</link><description>Vienna, Austria, March 18, 2013 / B3C newswire / - Anagrelide a selective platelet lowering agent is not inferior compared to hydroxyurea in preventing disease related complications in patients with WHO-ET. ANAHYDRET study data now provide evidence that anagrelide can be considered as first line therapy for lowering of platelet count in WHO-ET.&lt;/p&gt;&lt;p&gt;High platelet counts in essential thrombocythemia...</description><pubDate>Mon, 18 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Sinovac Biotech Ltd. Vaccine for Hand, Foot and Mouth Disease Meets Study Goal  </title><link>http://www.chinabiotoday.com/articles/20130314</link><description>BEIJING&lt;/span&gt;, &lt;span class"xn-chron"&gt;March 14, 2013&lt;/span&gt; /PRNewswire/ -- Sinovac Biotech Ltd. (NASDAQ: SVA), a leading provider of vaccines in &lt;span class"xn-location"&gt;China&lt;/span&gt;, announced today preliminary top-line data from its Phase III clinical trial assessing the efficacy, immunogenicity and safety of the Company's proprietary Enterovirus 71 ("EV71") vaccine against hand, foot and mouth...</description><pubDate>Fri, 15 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Marinomed Biotechnologie GmbH Release: Antiviral Nasal Spray - Data From Two Clinical Studies Prove Effectiveness of Marinomed's Antiviral Drug  </title><link>http://www.biospace.com/news_story.aspx?StoryID=290691&amp;full=1</link><description>Vienna, March 15, 2013 - The pooled analysis of data from two clinical studies has once again proven the effectiveness of an innovative antiviral nasal spray used to treat the common cold. Both the duration of cold infections and the number of patients with symptoms were clearly reduced by the use of the nasal spray developed by the Viennese biotech company Marinomed. The effectiveness of the safe...</description><pubDate>Fri, 15 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>BioAlliance Pharma Pursues the Development Plan of Its Loramyc&amp;#0174; in Japan Through Its Partner Sosei  </title><link>http://www.biospace.com/news_story.aspx?StoryID=290290&amp;full=1</link><description>Paris, March 12, 2013 - BioAlliance Pharma SA (Euronext Paris - BIO), an innovative Company dedicated to the development of orphan oncology products and to supportive care products, announces the initiation of Loramyc/Oravig Phase III clinical trial for the treatment of oropharyngeal candidiasis  by its Japanese partner Sosei. This is the final step before registration of the drug by Japanese authorities...</description><pubDate>Tue, 12 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Gilead Sciences, Inc. Drug Reduces Chest Pain Episodes in Diabetics: Study  </title><link>http://www.biospace.com/news_story.aspx?StoryID=289994&amp;full=1</link><description>SAN FRANCISCO--(BUSINESS WIRE)-- Gilead Sciences, Inc. (GILD) today announced data from the Phase 4 TERISA (Type 2 Diabetes Evaluation of Ranolazine In Subjects With Chronic Stable Angina) study, which demonstrated that the addition of ranolazine to background antianginal therapy in chronic angina patients with type 2 diabetes significantly reduced the frequency of weekly angina episodes compared to...</description><pubDate>Mon, 11 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Eisai Inc. Slams German Decision on Fycompa; Takeda Pharmaceutical Co. Ltd. Files Vedolizumab With European Medicines Agency  </title><link>http://www.thepharmaletter.com/file/120555/eisai-slams-german-decision-on-fycompa-takeda-files-vedolizumab-with-ema.html</link><description>The German Federal Joint Committee (G-BA), the decision-making body of the self-governing medical system in Germany, has that it considers the additional benefit of Japanese drug major Eisais (TYO: 4523) epilepsy drug Fycompa (perampanel) unproven when compared to two other treatments as defined by the G-BA. CS PharmaValues NPV Analysts at Credit Suisse have a net present value for Fycompa in Europe...</description><pubDate>Mon, 11 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Bayer AG, Johnson &amp; Johnson Eye Wider Use for Xarelto With New Trials  </title><link>http://www.biospace.com/news_story.aspx?StoryID=289886&amp;full=1</link><description>Berlin, Germany, March 8, 2013 -Bayer HealthCare announced today the initiation of the PIONEER AF-PCI study, a Phase IIIb clinical study of its oral anticoagulant Xarelto (rivaroxaban) to investigate how best to treat patients with non-valvular atrial fibrillation (AF) who undergo percutaneous coronary intervention (PCI) with stent placement.&lt;/p&gt;&lt;p&gt;The PIONEER AF-PCI study will enroll approximately...</description><pubDate>Fri, 08 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Teva Pharmaceutical Industries Limited Holds Its Breath During Third Phase 3 Trial  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130306005054&amp;newsLang=en</link><description>JERUSALEM &amp; LUND, Sweden, Mar 06, 2013 (BUSINESS WIRE) -- Teva Pharmaceutical Industries Ltd. TEVA 3.32% and Active Biotech (nasdaq omx nordic:ACTI) announced today enrollment of the first patient in the CONCERTO study - the third Phase III placebo-controlled study designed to evaluate the efficacy, safety and tolerability of once-daily oral laquinimod in patients with relapsing-remitting multiple...</description><pubDate>Fri, 08 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>UCB, Inc. Had Positive Trial for Vimpat as Monotherapy  </title><link>http://www.biospace.com/news_story.aspx?StoryID=289442&amp;full=1</link><description>ATLANTA&lt;/span&gt; and &lt;span class"xn-location"&gt;BRUSSELS&lt;/span&gt;, March 5, 2013 /PRNewswire/ --&lt;b&gt; regulated information &lt;/b&gt; UCB today announced positive results of a Phase 3 study designed to evaluate the efficacy and safety of conversion to lacosamide monotherapy in adult patients with partial-onset seizures with or without secondary generalization compared with a historical control. The study met its...</description><pubDate>Tue, 05 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Teva Pharmaceutical Industries Limited Publishes Results From Milprosa Phase 3  </title><link>http://www.biospace.com/news_story.aspx?StoryID=289250&amp;full=1</link><description>JERUSALEM--(BUSINESS WIRE)-- Teva Pharmaceutical Industries Ltd. (TEVA) today announced the publication of results of the Phase III clinical trial of Milprosa (progesterone) vaginal ring in Fertility and Sterility. The study compared the efficacy and safety of once-weekly Milprosa to daily 8 percent progesterone vaginal gel for luteal phase support in in vitro fertilization (IVF) and found that clinical...</description><pubDate>Mon, 04 Mar 2013 12:00:00 AM GMT</pubDate></item><item><title>Alchemia Completes Enrolment in Pivotal Phase III HA-Irinotecan Trial of Metastatic Colorectal Cancer  </title><link>http://www.biospace.com/news_story.aspx?StoryID=289000&amp;full=1</link><description>&lt;div id"releaseBody"&gt;&lt;p&gt;BRISBANE, AUSTRALIA--(Marketwire - February  28, 2013) -  &lt;p&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;415 patients recruited; recruitment now closed &lt;/li&gt;&lt;li&gt;Participation in sub-study outperformed expectations &lt;/li&gt;&lt;li&gt;Results expected early 2014 &lt;/li&gt;&lt;/ul&gt;&lt;p&gt;Brisbane drug discovery and development company Alchemia Limited (ASX: ACL) has completed enrolment of patients in a pivotal Phase...</description><pubDate>Thu, 28 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Boehringer Ingelheim Corporation Announces Initiation of Pivotal Trial Investigating Volasertib in Patients With Acute Myeloid Leukaemia  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.ab520ce17e34ab71ff00d635c0908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130228005464&amp;newsLang=en</link><description>INGELHEIM, Germany--(BUSINESS WIRE)--With the enrollment of the first patient, Boehringer Ingelheim is pleased to announce on international Rare Disease Day, the initiation of a Phase III study (POLO-AML-2) investigating volasertib*, a selective and potent polo-like kinase (Plk) inhibitor, in combination with chemotherapy, in patients with acute myeloid leukaemia (AML) ineligible for intensive therapy...</description><pubDate>Thu, 28 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Merck KGaA Drug Fails in Late-Stage Brain Cancer Trial  </title><link>http://www.rttnews.com/2063322/merck-kgaa-late-stage-trial-of-cilengitide-fails-to-meet-primary-endpoint.aspx?type=qf&amp;utm_source=google&amp;utm_campaign=sitemap</link><description>Merck KGaAs (MRK) experimental tumor- fighting drug cilengitide failed to help patients with a form of brain cancer in a late-stage clinical trial, adding to recent drug-development setbacks for the company. The medicine didnt significantly increase survival in patients with newly diagnosed glioblastoma when added to standard chemotherapy, the Darmstadt, Germany-based drugmaker said in a statement...</description><pubDate>Tue, 26 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>ANTISENSE PHARMA GmbH Announces Revised Development Path for Trabedersen  </title><link>http://www.biospace.com/news_story.aspx?StoryID=288718&amp;full=1</link><description>Regensburg, Germany, February 26, 2013 / B3C newswire / - The biopharmaceutical company Antisense Pharma GmbH, today announced its revised corporate and development strategy, receiving full support from its main investors.&lt;/p&gt;&lt;p&gt;The updated corporate strategy focuses on streamlining the organization to meet its current business objectives and strengthen key senior management positions in light of...</description><pubDate>Tue, 26 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>CEL-SCI Announces Initiation of New Sites for Multikine Phase III Clinical Study for Head and Neck Cancer in Taiwan  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130225006100&amp;newsLang=en</link><description>VIENNA, Va.--(BUSINESS WIRE)--CEL-SCI Corporation (NYSE MKT: CVM) announced today that its Taiwanese partner, Orient Europharma, has added two additional Taiwanese clinical centers in CEL-SCIs Phase III head and neck cancer clinical trial for Multikine (Leukocyte Interleukin, Injection), the Companys flagship investigational immunotherapy. The first center is the China Medical University Hospital...</description><pubDate>Mon, 25 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Algeta: Further Sub-Analyses of ALSYMPCA Phase III Study Presented at  </title><link>http://www.biospace.com/news_story.aspx?StoryID=287844&amp;full=1</link><description>&lt;div id"releaseBody"&gt;&lt;p&gt;OSLO, NORWAY--(Marketwire - February  15, 2013) -  &lt;p&gt;&lt;br&gt;Intended for US Media only&lt;p&gt;Abstracts #11 &amp;amp; #19&lt;p&gt;Algeta ASA (OSE: ALGETA) announces that furthersub-analyses of data from the phase III ALSYMPCA study of radium Ra 223dichloride (radium-223) in castration-resistant prostate cancer (CRPC)patientshave been presented at the 2013 Genitourinary Cancers...</description><pubDate>Fri, 15 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Astellas Pharma Inc. and AVEO Oncology (Formerly known as AVEO Pharmaceuticals, Inc.) Report Positive Kidney Cancer Drug Trial Data  </title><link>http://www.biospace.com/news_story.aspx?StoryID=287495&amp;full=1</link><description>CAMBRIDGE, Mass. and TOKYO, Japan, February 12, 2013 - AVEO Oncology (NASDAQ: AVEO) and Astellas Pharma Inc. (TSE: 4503) today announced overall survival (OS) for tivozanib, an investigational agent, from the Phase 3 TIVO-1 (TIvozanib Versus sOrafenib in 1st line advanced RCC) study in patients with advanced renal cell carcinoma (RCC). The final OS analysis, as specified by the protocol, shows a median...</description><pubDate>Thu, 14 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Pozen, Inc. Presents Positive Phase 3 Results  </title><link>http://www.biospace.com/news_story.aspx?StoryID=287156&amp;full=1</link><description>HONOLULU--(BUSINESS WIRE)-- POZEN Inc. (POZN), a pharmaceutical company committed to transforming medicine that transforms lives, presented data today from the combined results of two Phase 3 studies of PA32540, an antiplatelet therapy of enteric-coated (EC) and immediate-release omeprazole, in patients with previous cerebrovascular disease. These data were presented at the American Heart Association...</description><pubDate>Fri, 08 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Biogen Idec, Inc. (Massachusetts) Release: New Phase 3 Data Reinforce Long-Lasting Protection From Bleeding for Patients With Hemophilia A and B  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.ab520ce17e34ab71ff00d635c0908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130208005166&amp;newsLang=en</link><description>WARSAW, Poland--(BUSINESS WIRE)--Biogen Idec (NASDAQ: BIIB) and Swedish Orphan Biovitrum (Sobi) (STO: SOBI) released data that confirmed the ability of investigational recombinant factors VIII Fc fusion protein (rFVIIIFc) and IX Fc fusion protein (rFIXFc) to provide long-lasting protection from bleeding with fewer injections than are required with the current standard of care for people with hemophilia...</description><pubDate>Fri, 08 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Genentech Says Blood Cancer Drug Met Stage One Goal  </title><link>http://www.reuters.com/article/2013/01/31/roche-ga-idUSL5N0B01HF20130131</link><description>Roche's GA101 drug significantly improved progression-free survival in people with chronic lymphocytic leukaemia (CLL), giving the Swiss drugmaker the first signal it may have a viable successor to its current best-selling medicine. Roche is banking on the success of GA101 to fend off the threat of so-called biosimilar copies of cancer treatment MabThera, its top seller in 2012 with sales of 6.7 billion...</description><pubDate>Mon, 04 Feb 2013 12:00:00 AM GMT</pubDate></item><item><title>Celgene's Abraxane  Keeps Pancreatic Pts Alive an Extra Two Months in Trial  </title><link>http://www.biospace.com/news_story.aspx?StoryID=285434&amp;full=1</link><description>BOUDRY, Switzerland--(BUSINESS WIRE)-- Celgene International Srl, a subsidiary of Celgene Corporation (CELG), today announced that its phase III clinical trial of ABRAXANE (paclitaxel protein-bound particles for injectable suspension) (albumin-bound) in combination with gemcitabine in treatment-nave patients with metastatic pancreatic cancer demonstrated a statistically significant improvement in...</description><pubDate>Thu, 24 Jan 2013 12:00:00 AM GMT</pubDate></item><item><title>Teva Pharmaceutical Industries Limited's NUVIGIL&amp;#0174; Fails Phase 3 Trial Again  </title><link>http://www.biospace.com/news_story.aspx?StoryID=285465&amp;full=1</link><description>JERUSALEM--(BUSINESS WIRE)-- Teva Pharmaceutical Industries Ltd. today announced top-line results of its Phase III clinical program for armodafinil (NUVIGIL) as adjunct therapy in adults with major depression associated with bipolar 1 disorder. While study 3072 demonstrated a numerical improvement, it did not reach statistical significance in meeting its primary endpoint -- to determine whether armodafinil...</description><pubDate>Wed, 23 Jan 2013 12:00:00 AM GMT</pubDate></item><item><title>Amarin Corporation PLC Announces Publication of Additional Inflammatory Marker Data From MARINE and ANCHOR Phase 3 Clinical Trials in the /i&gt;  </title><link>http://www.globenewswire.com/news-release/2013/01/22/517649/10018103/en/Amarin-Announces-Publication-of-Additional-Inflammatory-Marker-Data-From-MARINE-and-ANCHOR-Phase-3-Clinical-Trials-in-the-American-Journal-of-Cardiovascular-Drugs.html</link><description>BEDMINSTER, N.J. and DUBLIN, Ireland, Jan. 22, 2013 (GLOBE NEWSWIRE) -- Amarin Corporation plc (Nasdaq:AMRN), a biopharmaceutical company focused on the commercialization and development of therapeutics to improve cardiovascular health, announced today that additional data from its pivotal MARINE and ANCHOR Phase 3 clinical trials are now available electronically through PubMed (available at: http...</description><pubDate>Tue, 22 Jan 2013 12:00:00 AM GMT</pubDate></item><item><title>&lt;b&gt;Synthon Biopharmaceuticals&lt;/b&gt; Reports Positive Early Results With Its Second Generation HER2-Antibody-Drug Conjugate  </title><link>http://www.businesswire.com/portal/site/biospace/template.PAGE/menuitem.ab520ce17e34ab71ff00d635c0908a0c/index.jsp?ndmViewId=news_view&amp;newsId=20130122005270&amp;newsLang=en</link><description>NIJMEGEN, the Netherlands--(BUSINESS WIRE)--Synthon Biopharmaceuticals, a subsidiary of specialty pharma company Synthon, has reported promising results with its lead program of antibody-drug conjugates (ADCs). In pre-clinical xenograft studies using patient-derived breast cancer and non-small-cell lung cancer material, Synthon has reported complete tumor remission. Toxicity experiments conducted to...</description><pubDate>Tue, 22 Jan 2013 12:00:00 AM GMT</pubDate></item><item><title>Boehringer Ingelheim Corporation Enrolls First Patients in Pivotal Phase III Interferon-Free Hepatitis C Trial Program  </title><link>http://www.businesswire.com/portal/site/biospace/index.jsp?ndmViewId=news_view&amp;newsId=20130117005088&amp;newsLang=en</link><description>INGELHEIM, Germany--(BUSINESS WIRE)--Today, Boehringer Ingelheim announced that the first patients have been enrolled in the companys pivotal Phase III interferon (IFN)-free hepatitis C (HCV) clinical trial programme, HCVerso. Boehringer Ingelheims IFN-free investigational polymodal* regimen combines faldaprevir (BI 201335), a next wave once-daily protease inhibitor, and BI 207127, a non-nucleoside...</description><pubDate>Thu, 17 Jan 2013 12:00:00 AM GMT</pubDate></item><item><title>Eisai Company, Ltd.'s Farletuzumab Fails Ovarian Cancer Trial  </title><link>http://www.thepharmaletter.com/file/119304/eisaimorphoteks-farletuzumab-fails-on-ovarian-cancer-ph-iii-trial.html</link><description>The FAR-131 trial of farletuzumab  developed by Eisai's US subsidiary Morphotek  showed that the drug was unable to improve progression-free survival (PFS) in patients with platinum-sensitive epithelial ovarian cancer who had suffered a first relapse. In the 1,100-patient study, farletuzumab at two doses or placebo were added to a background regimen of carboplatin and a taxane drug such as paclitaxel...</description><pubDate>Tue, 15 Jan 2013 12:00:00 AM GMT</pubDate></item><item><title>Zhifei Biological Products Approved to Begin China Phase III Trial of TB Vaccine  </title><link>http://www.chinabiotoday.com/articles/20130111</link><description>by Richard Daverman, PhD&lt;/p&gt;&lt;p&gt;January 11, 2013 -- Chongqing Zhifei Biological Product Co. has been granted SFDA approval to begin a Phase III trial of an existing product, Mycobacterium Vaccae for Injection (Vaccae), as a vaccine for tuberculosis, a currently unmet need. Vaccae is an immune system modulator that the company currently sells as an adjuvant to treat TB. More details....&lt;/p&gt;&lt;p...</description><pubDate>Fri, 11 Jan 2013 12:00:00 AM GMT</pubDate></item></channel></rss>