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New Research Grants, Product Launches, and Positive Clinical Study Results - Research Report on Boston Scientific, Cooper, Arena

 New Research Grants, Product Launches, and Positive Clinical Study Results -
 Research Report on Boston Scientific, Cooper, Arena Pharmaceuticals, Apricus
                      Biosciences, and NewLink Genetics

PR Newswire

NEW YORK, June 13, 2013

NEW YORK, June 13, 2013 /PRNewswire/ --

Editor Note: For more information about this release, please scroll to bottom.

Today, Wall Street Reports announced new research reports highlighting Boston
Scientific Corporation (NYSE: BSX), The Cooper Companies, Inc. (NYSE: COO),
Arena Pharmaceuticals, Inc. (NASDAQ: ARNA), Apricus Biosciences Inc. (NASDAQ:
APRI), and NewLink Genetics Corp. (NASDAQ: NLNK). Today's readers may access
these reports free of charge - including full price targets, industry analysis
and analyst ratings - via the links below.

Boston Scientific Corporation Research Report

On June 3, 2013, Boston Scientific Corporation (Boston Scientific) announced
that it will provide a research and education grant of more than $1 million to
the Pelvic Floor Disorders Networks (PFDN) for the SUPeR clinical trial. The
SUPeR study will evaluate the treatment outcomes of two different surgical
options for women with uterine prolapse, a form of pelvic organ prolapse. The
study will enroll 180 women who are considering surgery for their uterine
prolapse and do not plan to have any more children. They will be randomly
assigned to either a uterine-preserving transvaginal mesh repair using the
Boston Scientific Uphold LITE Vaginal Support System or traditional surgery
that will include a vaginal hysterectomy. The Full Research Report on Boston
Scientific Corporation - including full detailed breakdown, analyst ratings
and price targets - is available to download free of charge at:
[http://www.wsreports.com/r/full_research_report/5649_BSX]

--

The Cooper Companies, Inc. Research Report

On June 6, 2013, The Cooper Companies, Inc. (Cooper) announced its financial
results for Q2 FY 2013 (period ended April 30, 2013). Revenue increased 11.4%
YoY to $384 million. GAAP EPS increased 35.7% YoY to $1.52. Commenting on the
results, Robert S. Weiss, Cooper's President and Chief Executive Officer,
said, "I am enthused by our performance as we continue executing on our
long-range strategies that lead to gaining market share and improving our
operating margin." For full-year FY 2013, the Company expects revenue in the
range of $1,575 million to $1,605 million, and GAAP EPS in the range of $6.42
to $6.52. The Full Research Report on The Cooper Companies, Inc. - including
full detailed breakdown, analyst ratings and price targets - is available to
download free of charge at:
[http://www.wsreports.com/r/full_research_report/9fd9_COO]

--

Arena Pharmaceuticals, Inc. Research Report

On June 7, 2013, Arena Pharmaceuticals, Inc. (Arena Pharmaceuticals) reported
the launch of BELVIQ in the United States. The product will be available to
patients by prescription in US pharmacies beginning June 11, 2013. Eisai Inc.
(Eisai) is responsible for the marketing and distribution of BELVIQ under its
agreement with Arena Pharmaceuticals GmBH, a wholly-owned subsidiary of Arena
Pharmaceuticals. The Company reported that it manufactures BELVIQ at its
manufacturing facility in Switzerland and sells the finished commercial
product to Eisai for a purchase price starting at 31.5% of Eisai's annual net
product sales. The purchase price increases on a tiered basis of up to 36.5%
on the portion of annual net product sales exceeding $750 million. In relation
with the US launch of BELVIQ, Arena has received $65 million in milestones
from Eisai. Further, Eisai has submitted a marketing authorization application
for BELVIQ in Mexico and plans to submit applications for the approval of
BELVIQ in Canada and Brazil in 2013. The Full Research Report on Arena
Pharmaceuticals, Inc. - including full detailed breakdown, analyst ratings and
price targets - is available to download free of charge at:
[http://www.wsreports.com/r/full_research_report/6991_ARNA]

--

Apricus Biosciences Inc. Research Report

On June 10, 2013, Apricus Biosciences Inc. (Apricus Bio) announced that its
marketing application for Vitaros, indicated for the treatment of patients
with erectile dysfunction (ED), has been approved through the European
Decentralized Procedure (DCP). Commenting on the approval, Richard Pascoe,
Chief Executive Officer of Apricus Bio, said, "With its rapid onset of action
and unique topical delivery, we believe that Vitaros will capture a
significant share of the approximately $1 billion PDE-5 inhibitor market in
Europe once it is launched by our commercial partners." Under the DCP, the
Company filed its application for marketing approval designating Netherlands
as the Reference Member State (RMS) on behalf of nine other European Concerned
Member States (CMS) participating in the procedure. The CMS include France,
Germany, Italy, UK, Ireland, Spain, Sweden, Belgium, and Luxembourg. Apricus
Bio will continue to work independently as well as with its commercialization
partners, Sandoz, Takeda, and Bracco for the next step of obtaining national
phase approvals in order to make Vitaros ready to launch in each of the
included territories across Europe. The Full Research Report on Apricus
Biosciences Inc. - including full detailed breakdown, analyst ratings and
price targets - is available to download free of charge at:
[http://www.wsreports.com/r/full_research_report/2aca_APRI]

--

NewLink Genetics Corp. Research Report

On June 3, 2013, NewLink Genetics Corporation (NewLink Genetics) announced
results from a Phase 2 clinical study with its drug candidate algenpantucel-L.
The study evaluated algenpantucel-L plus standard-of-care adjuvant therapy
(gemcitabine and 5-FU-modulated radiation therapy) in 69 patients with
resected pancreatic cancer. The study defined disease-free survival at one
year as its primary endpoint, and overall survival, safety, and immunological
correlative analysis as the secondary endpoints. The data showed that one year
disease-free survival was 62%, while overall survival was 86%. Specifically,
the data showed median overall survival was 42 months in patients with
elevated levels of anti-mesothelin antibodies versus 20 months in patients
without elevated levels. Moreover, the subset of patients that showed
increases in two or more of the aforementioned biomarkers had median overall
survival greater than 42 months (median overall survival not reached for this
subset of patients). The Full Research Report on NewLink Genetics Corp. -
including full detailed breakdown, analyst ratings and price targets - is
available to download free of charge at:
[http://www.wsreports.com/r/full_research_report/c29b_NLNK]

----

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