Opinion Research

 
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2013/3/1
TORONTO, March 1, 2013 (GLOBE NEWSWIRE) -- GreeneStone Healthcare Corporation (OTCBB:GRST) , provider of Healthcare services and operator of several mental health clinics, announced that Ludlow Research has issued a research opinion on the company based on the expansion of addiction treatment centers, and the move towards profitability.
Sign-up for Ludlow Research Issues Opinion on GreeneStone Healthcare Based on Move Towards Profitability investment picks
2013/2/1
BOCA RATON, Fla., Feb.
Sign-up for Ludlow Research Issues Opinion on InterCloud Systems Based on Current Valuation investment picks
2013/3/12
Torontonians Voice Their Opinions About Toronto's Street Furniture Canada NewsWire Torontonians agree that Toronto's Coordinated Street Furniture Program is a role model for other Cities TORONTO , March 12, 2013 /CNW Telbec/ - To mark the five year anniversary of Toronto's Coordinated Street Furniture Program , Astral Out-of-Home asked Torontonians what they think of the program and new street furniture including bus shelters and benches.
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2013/3/22
LONDON , March 22, 2013 /PRNewswire/ -- Baxter International Inc. (NYSE: BAX) and Halozyme Therapeutics, Inc., (NASDAQ: HALO) today announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (EMA CHMP) has granted a Positive Opinion to Baxter for the use of HyQvia (solution for subcutaneous use) as replacement therapy for adult patients with primary and secondary immunodeficiencies.
Sign-up for Baxter And Halozyme Announce Positive Opinion For HyQvia For Treatment Of Primary And Secondary Immunodeficiencies In The European Union investment picks
2013/3/22
Baxter International Inc. (NYSE:BAX) and Halozyme Therapeutics, Inc., (NASDAQ:HALO) today announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (EMA CHMP) has granted a Positive Opinion to Baxter for the use of HyQvia (solution for subcutaneous use) as replacement therapy for adult patients with primary and secondary immunodeficiencies.
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2013/4/25
Pfizer Inc. (NYSE: PFE) announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a negative opinion for XELJANZ ® (tofacitinib citrate) for the treatment of adult patients with moderate-to-severe active rheumatoid arthritis (RA). The CHMP is of the opinion that XELJANZ does not demonstrate a favorable risk:benefit profile at this time and recommended against marketing authorization.
Sign-up for Pfizer Receives CHMP Negative Opinion Regarding Marketing Authorization In Europe For Rheumatoid Arthritis Treatment XELJANZ® (tofacitinib citrate) investment picks
2013/2/27
EASTERN AMERICAN NATURAL GAS TRUST (NYSE:NGT) (the “Trust”) announced today that it has filed a Schedule 14D-9 with the Securities and Exchange Commission stating that neither the Trust nor its trustee is making any recommendation or expressing any opinion, and both are remaining neutral, toward the exchange offer being made by Energy Corporation of America for Depositary Units of the Trust.
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2013/3/22
ARIAD Pharmaceuticals, Inc. (NASDAQ: ARIA) today announced that the Committee for Human Medicinal Products (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion on the marketing authorization application for Iclusig™ (ponatinib) for two indications: “The positive recommendation by the CHMP of Iclusig for use in CML and Ph+ALL provides a broad indication statement for Iclusig in resistant and intolerant patients with Philadelphia positive leukaemias, including many patients who have failed only one prior tyrosine kinase inhibitor,” stated Harvey J.
Sign-up for ARIAD Announces That Iclusig™ (Ponatinib) Receives Positive CHMP Opinion for Approval in the European Union investment picks
2013/3/22
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 Authorisation Application (MAA) for the once-daily, single tablet regimen Stribild ® for the treatment of HIV-1 infection in adult patients who are antiretroviral-naïve or are infected with HIV-1 without known mutations associated with resistance to any of the three antiretroviral agents in Stribild.
Sign-up for European CHMP Adopts Positive Opinion for Stribild®, a Once-Daily, Integrase Inhibitor-Based, Single Tablet Regimen for the Treatment of HIV-1 Infection investment picks
2013/3/22
VILLA GUARDIA, Italy, March 22, 2013 (GLOBE NEWSWIRE) -- Gentium S.p.A. (Nasdaq:GENT) (the "Company") announced today that it has been informed by the European Medicines Agency's ("EMA") Committee for Medicinal Products for Human Use ("CHMP") that it has adopted a negative opinion, recommending the refusal of the marketing authorization for Defibrotide to treat and prevent hepatic veno-occlusive disease ("VOD") in adults and children undergoing hematopoietic stem cell transplantation therapy.
Sign-up for Gentium Receives Negative Opinion From the CHMP on Defibrotide for the Treatment and Prevention of VOD investment picks
2013/3/22
Genzyme , a Sanofi Company (EURONEXT: SAN and NYSE: SNY) announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a positive opinion regarding the approval of once-daily, oral AUBAGIO ® (teriflunomide) for the treatment of adult patients with relapsing-remitting multiple sclerosis (MS). “The fact that AUBAGIO has demonstrated a positive effect on disability progression in two, phase III clinical studies underscores its importance as a new treatment option for relapsing-remitting MS patients,” said Professor Ludwig Kappos, MD, Chair of Neurology, University Hospital, Basel, Switzerland.
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2013/3/22
Today Biogen Idec (NASDAQ: BIIB) announced that it has received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) in the European Union (EU) recommending a marketing authorization be granted for TECFIDERA ™ (dimethyl fumarate) as a first-line oral treatment for adults with relapsing-remitting multiple sclerosis (RRMS). The CHMP, on the basis of quality, safety and efficacy data submitted by Biogen Idec, considers there to be a favorable benefit-to-risk balance for TECFIDERA.
Sign-up for CHMP Issues Positive Opinion for TECFIDERA™ (Dimethyl Fumarate) as a First-Line Treatment for Multiple Sclerosis in the European Union investment picks
2013/4/1
DALLAS , April 1, 2013 /PRNewswire/ -- The Hallwood Group Incorporated (NYSE MKT: HWG) reported that its audited consolidated financial statements for the fiscal year ended December 31, 2012 , included in the Company's Annual Report on Form 10-K, which was filed today with the Securities and Exchange Commission, contains an audit opinion from its independent public accounting firm which includes explanatory language related to going concern resulting from the uncertainty of the payment of dividends from its subsidiary to fund the Company's ongoing operations and obligations.
Sign-up for Hallwood Group Receives Audit Opinion With Going Concern Explanation And Reports Results For The Fourth Quarter And Year Ended December 31, 2012 investment picks
2013/4/16
VILLA GUARDIA, Italy, April 16, 2013 (GLOBE NEWSWIRE) -- Gentium S.p.A. (Nasdaq:GENT) (the "Company") today announced that it has requested a re-examination of the negative opinion adopted, by the European Medicines Agency's ("EMA") Committee for Medicinal Products for Human Use ("CHMP"), on March 22 nd , regarding the Marketing Authorisation (MAA) submitted for Defibrotide to treat and prevent hepatic veno-occlusive disease ("VOD") in adults and children undergoing hematopoietic stem cell transplantation therapy.
Sign-up for Gentium to Request Re-Examination of CHMP Opinion on Defibrotide investment picks
2013/4/26
Today, Astellas Pharma Europe Ltd., the European Headquarters of Tokyo-based Astellas Pharma Inc. (TSE:4503), and Medivation, Inc. (Nasdaq: MDVN) have received a positive opinion from the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP), recommending European Commission (EC) approval for XTANDI ® (enzalutamide) capsules for the treatment of adult men with metastatic castration-resistant prostate cancer whose disease has progressed on or after docetaxel therapy.
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2013/5/17
PPG Industries (NYSE:PPG) today announced that the United States Bankruptcy Court for the Western District of Pennsylvania issued an opinion and interim order confirming the current Pittsburgh Corning plan of reorganization.
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2013/3/11
http://at.marketwire.com/accesstracking/AccessTrackingLogServlet?PrId=994826&ProfileId=051205&sourceType=1 NEWPORT BEACH, CA --
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2013/3/1
http://media.marketwire.com/attachments/201202/15004_11767_LifeSciAdvisors01-31-2012.jpg http://at.marketwire.com/accesstracking/AccessTrackingLogServlet?PrId=992101&ProfileId=051205&sourceType=1 NEW YORK, NY --
Sign-up for LifeSci Advisors Announces Investment Opinion on Adherex Technologies investment picks
2013/2/19
MCLEAN, Va.
Sign-up for USA TODAY To Collaborate With Pew Research Center On Public Opinion Polling investment picks
2013/2/26
SAN DIEGO , Feb.
Sign-up for Encore Capital Addresses Sixth Circuit Opinion investment picks

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Opinion Research
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