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Research Abstracts, Phase 2 Results, and Market Availability of Formulations and Treatments- Research Report on Teva, Forest,



 Research Abstracts, Phase 2 Results, and Market Availability of Formulations
 and Treatments- Research Report on Teva, Forest, Pharmacyclics, Cubist, and
                                 Dr. Reddy's

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

PR Newswire

NEW YORK, June 19, 2013

NEW YORK, June 19, 2013 /PRNewswire/ --

Today, Wall Street Reports announced new research reports highlighting Teva
Pharmaceutical Industries Ltd (NYSE: TEVA), Forest Laboratories, Inc. (NYSE:
FRX), Pharmacyclics, Inc. (NASDAQ: PCYC), Cubist Pharmaceuticals, Inc.
(NASDAQ: CBST), and Dr. Reddy's Laboratories Limited (NYSE: RDY). Today's
readers may access these reports free of charge - including full price
targets, industry analysis and analyst ratings - via the links below.

Teva Pharmaceuticals Industries Ltd Research Report

On June 14, 2013, Teva Pharmaceuticals Industries Ltd (Teva) announced that
the Company will present a number of abstracts during the 17th Annual
International Congress of Parkinson's Disease and Movement Disorders, held in
Sydney, Australia from June 16 to June 20, 2013. The Company affirmed that
these presentations will reflect Teva's ongoing commitment to Parkinson's
Disease (PD) research and underscore the potential of AZILECT as a treatment
modality for PD. "We are committed to driving advances in research to help
address the treatment needs of those impacted by neurological conditions,"
said Michael Hayden, MD, President of Global R&D and Chief Scientific Officer
at Teva.  The Full Research Report on Teva Pharmaceuticals Industries Ltd -
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/e4ac_TEVA]

--

Forest Laboratories, Inc. Research Report

On June 13, 2013, Forest Laboratories, Inc. (Forest) announced the
availability of NAMENDA XR (memantine hydrochloride) once-daily formulation,
in pharmacies throughout the United States. NAMENDA XR is approved by the FDA
for the treatment of moderate to severe dementia of the Alzheimer's type. The
efficacy and safety of the formulation was established in a randomized,
double-blind, placebo-controlled trial of 677 outpatients on a stable dose of
acetylcholinesterase inhibitors (AChEI). The results of the study demonstrated
statistically significant improvement in cognition and global function for
patients treated with NAMENDA XR 28 mg plus an AChEI compared to placebo plus
an AChEI. "The NAMENDA XR study supports the existing body of evidence that
memantine provides cognitive and global benefits in patients with moderate to
severe Alzheimer's disease either alone or with an AChEI," said Dr. Marco
Taglietti, President of Forest Research Institute. The Full Research Report on
Forest Laboratories, 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/e121_FRX]

--

Pharmacyclics, Inc. Research Report

On June 16, 2013, Pharmacyclics, Inc. (Pharmacyclics) announced the results of
two separate Phase 2 studies suggesting that ibrutnib showed efficacy when
used as a monotherapy in patients with relapsed/refractory mantle cell
lymphoma (MCL) or diffuse large B-cell lymphoma (DLBCL). The Company sponsored
both studies and is jointly developing ibrutnib with Janssen Research &
Development, LLC. The findings at EHA for patients with MCL or DLBCL expand on
the results reported by investigators in 2012. Among patients with
relapsed/refractory MCL, ibrutnib achieved an overall response rate (ORR) of
68%, including a complete response (CR) of 21% where all signs of cancer are
gone, and a partial response (PR) of 47%. In the second study among
relapsed/refractory DLBCL patients, investigators examined whether ibrutinib
would be more active in the Activated B-cell-like (ABC) subtype of DBCL
compared to those with the Germinal Center B-Cell-like (GCB) subtype. Results
revealed that patients with the ABC subtype showed a preferential response to
ibrutinib monotherapy compared to those with the GCB subtype, with ORR
response rate of 41% vs. 5%, respectively. The Full Research Report on
Pharmacyclics, 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/dd7a_PCYC]

--

Cubist Pharmaceuticals, Inc. Research Report

On June 13, 2013, Cubist Pharmaceuticals, Inc. (Cubist) announced the
appointment of Dr. Lorianne Masuoka as Chief Medical Officer and Senior Vice
President of Clinical Development and Medical Affairs. With the new
appointment, Dr. Masuoka will lead the strategy, development, and
implementation of the Company's global clinical programs, while overseeing
Clinical Research, Medical Affairs, Clinical Operations, Biostatistics, Data
Management, and Pharmacovigilance. "Dr. Masuoka brings to Cubist a great blend
of medical and scientific leadership, diversity of therapeutic area
experience, and global management skills," said Steven Gilman, Ph.D.,
Executive Vice President of Research and Development and Chief Scientific
Officer of Cubist. Dr. Masuoka has more than 25 years of global medical and
development experience. Previously, she has served in many roles, including as
Senior Vice President and Chief Medical Officer at Nektar Therapeutics, VP of
Clinical Development at Fiveprime Therapeutics, and Director of Clinical
Development at Chiron. The Full Research Report on Cubist 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/92f0_CBST]

--

Dr. Reddy's Laboratories Limited Research Report

On June 3, 2013, Dr. Reddy's Laboratories Limited (Dr. Reddy's) and Fujifilm
Corporation (Fujifilm) announced the termination of their Memorandum of
Understanding (MoU) to enter into an exclusive partnership in the generic
drugs business for the Japanese market and to establish a joint venture in
Japan. The MoU was signed on July 28, 2011, based on which the two Companies
had conducted detailed studies on the establishment of a joint venture for
developing and manufacturing generic drugs in Japan. However, the Company
stated that as Fujifilm is realigning its long-term growth strategy, both
Companies have agreed on terminating the MoU. "Unfortunately, we will not be
able to partner with Fujifilm specifically for generic formulations business
in Japan. However, I want to reinforce our commitment towards a planned entry
into Japan to bring affordable and innovative drugs to more patients
worldwide," said GV Prasad, Chairman and CEO of Dr. Reddy's. The Full Research
Report on Dr. Reddy's Laboratories Limited - 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/e286_RDY]

----

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SOURCE Wall Street Reports
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