Opinion Research

 
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2014/9/2
Council of Ministers Issues Favorable Opinion on Planned Sale of Stock Participation of Ecopetrol S.A. in Empresa de Energia de Bogota S.A. E.S.P. Canada NewsWire BOGOTA, Colombia , Sept.
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Gilead Sciences, Inc. (NASDAQ:GILD) today announced that the Committee for Medicinal Products for Human Use (CHMP), the scientific committee of the European Medicines Agency (EMA), has adopted a positive opinion on the company’s Marketing Authorization Application (MAA) for Zydelig ® (idelalisib 150 mg film-coated tablets), a first-in-class treatment for patients with chronic lymphocytic leukemia (CLL) and follicular lymphoma (FL), the most common subtype of indolent non-Hodgkin lymphoma (iNHL). The CHMP opinion supports the use of Zydelig in combination with rituximab for the treatment of adult patients with CLL who have received at least one prior therapy or, as first-line treatment in CLL patients in the presence of 17p deletion or TP53 mutation in patients unsuitable for chemo-immunotherapy and also as monotherapy for the treatment of adult patients with FL that is refractory to
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2014/8/8
http://at.marketwire.com/accesstracking/AccessTrackingLogServlet?PrId=11G019673-001&sourceType=1 http://www.marketwire.com/library/MwGo/2014/8/7/11G019673/WR_RGB-70425602538.jpg PARSIPPANY, NJ--(Marketwired - August 08, 2014) - Looking for a quick and easy way to boost your Wyndham Rewards point balance this summer?
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2014/9/5
By Paul Kiernan RIO DE JANEIRO--Brazilian stocks snapped a three-session winning streak and closed lower Friday as investors awaited results of a new public-opinion poll on the country's October presidential elections.
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Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced that the European Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion recommending the approval of KALYDECO™ (ivacaftor) for people with cystic fibrosis (CF) ages 6 and older who have one of eight non-G551D gating mutations in the cystic fibrosis transmembrane conductance regulator ( CFTR ) gene.
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Bristol-Myers Squibb Company (NYSE:BMY) and Pfizer Inc. (NYSE:PFE) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending that Eliquis (apixaban) be granted marketing authorization for the treatment of DVT (deep vein thrombosis) and PE (pulmonary embolism), and the prevention of recurrent DVT and PE, in adults.
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Bristol-Myers Squibb Company (NYSE:BMY) today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending that Daklinza ® (daclatasvir), an investigational, potent pan-genotypic NS5A complex inhibitor (in vitro) , be granted approval for use in combination with other medicinal products for the treatment of chronic hepatitis C virus (HCV) infection in adults.
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OPKO Health, Inc. (NYSE:OPK) today announced that the European Committee for Orphan Medicinal Products (COMP) gave a positive opinion recommending the approval of orphan drug designation for OPKO's long-acting version of clotting Factor VIIa (Factor VIIa-CTP) for the treatment of bleeding episodes in patients with hemophilia A or B with inhibitors to Factor VIII or Factor IX and congenital Factor VII deficiency.
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NEW YORK (MarketWatch) -- Bristol Myers-Squibb Co.
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Allergan, Inc. (NYSE: AGN) announced today that the European Union’s Committee for Medicinal Products for Human Use (CHMP) has recommended extending the Marketing Authorization for OZURDEX ® (dexamethasone 700 mcg intravitreal implant in applicator) to treat adult patients with vision loss due to diabetic macular edema (DME) who are pseudophakic (have an artificial lens implant), or who are considered insufficiently responsive to, or unsuitable for non-corticosteroid therapy.
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2014/9/11
ELKHART, Ind.
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Opinion Research
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