FDA Approvals, Stock Price Movements, and Study Results - Research Report on Pfizer, Celgene, Merck, Quest Diagnostics, and Pharmacyclics

NEW YORK, November 21, 2013 /PRNewswire/ --

Today, Analysts' Corner announced new research reports highlighting Pfizer Inc. (NYSE: PFE), Celgene Corporation (NASDAQ: CELG), Merck & Co., Inc. (NYSE: MRK), Quest Diagnostics Inc. (NYSE: DGX) and Pharmacyclics, Inc. (NASDAQ: PCYC). Today's readers may access these reports free of charge - including full price targets, industry analysis and analyst ratings - via the links below.

Pfizer Inc. Research Report

On November 18, 2013, Pfizer Inc. (Pfizer) announced that the U.S. Food and Drug Administration (FDA) approved the supplemental New Drug Application (sNDA) for XELJANZ (tofacitinib citrate) to include additional Patient-Reported Outcomes (PRO) data in the label. According to Pfizer, these additional data show improvement in patients receiving XELJANZ based on health-related outcome measures reported by patients, including vitality, role emotional, physical function, bodily pain, social function, mental health, role physical and general health, which are the eight domains of the Medical Outcomes Study Short-Form (36-Item) Health Survey (SF-36). Dr. Steven Romano, Senior Vice President and Head of the Medicines Development Group for Pfizer Specialty Care, said, "The patient-reported outcomes data show the impact that XELJANZ can have on the daily lives of patients with RA, based on physical, mental and emotional measures. Following the FDA approval of XELJANZ in November 2012, we are pleased with the agency's decision to approve this sNDA and add to the growing body of knowledge about XELJANZ as an additional treatment option for patients with RA." The Full Research Report on Pfizer Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at:

http://www.analystscorner.com/r/full_research_report/d702_PFE

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Celgene Corporation Research Report

On November 18, 2013, Celgene Corporation's (Celgene) stock rose 1.24%, ending the day at $152.98. Over the previous three trading sessions, shares of Celgene gained 2.48% compared to the Nasdaq Composite which declined 0.42% during the same period. The Full Research Report on Celgene Corporation - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at:

http://www.analystscorner.com/r/full_research_report/7f47_CELG

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Merck & Co., Inc. Research Report

On November 18, 2013, Merck & Co., Inc. (Merck) announced that its New Drug Application (NDA) for an investigational intravenous (IV) solution formulation of the Company's antifungal agent, NOXAFIL (posaconazole) has been accepted for priority review by the U.S. Food and Drug Administration (FDA). According to the Company, priority review designation is assigned to application for drugs that, if approved, would provide significant improvements in the safety and effectiveness of the treatment, diagnosis, or prevention of serious conditions. In addition, Merck informed that it has filed a marketing authorization application for NOXAFIL IV solution with the European Medicines Agency (EMA) and plans to seek regulatory approval for the IV formulation in other countries around the world. The Full Research Report on Merck & Co., Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at:

http://www.analystscorner.com/r/full_research_report/430d_MRK

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Quest Diagnostics Inc. Research Report

On November 18, 2013, Quest Diagnostics Inc. (Quest Diagnostics) released the results of a landmark analysis of workplace drug test. According to the Company, the Drug Testing Index (DTI) examined more than 125 million urine drug tests performed by the Company's forensic toxicology laboratories across the United States as a service for government and private employers between 1988 and 2012. The index reported the percentage of results that tested positive for the presence of a drug or its metabolite, an adulterant or that involved a specimen that was deemed to be unacceptable for testing (positivity). The key findings from the analysis released by the Company suggest that: the positivity rate for the combined U.S. workforce declined 74% from 13.6% in 1988 to 3.5% in 2012; the positivity rate for the federally-mandated safety sensitive workforce declined by 38% from 2.6% in 1992 to 1.6% in 2012; and the positivity rate for the U.S. general workforce declined by 60% from 10.3% in 1992 to 4.1% in 2012. The Full Research Report on Quest Diagnostics Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at:

http://www.analystscorner.com/r/full_research_report/05ba_DGX

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Pharmacyclics, Inc. Research Report

On November 13, 2013, Pharmacyclics Inc. (Pharmacyclics) announced that the U.S. Food and Drug Administration (FDA) has approved IMBRUVICA (ibrutinib) as a single agent for the treatments of patients with mantle cell lymphoma (MCL) who have received at least one prior therapy. According to the Company, IMBRUVICA is a new agent that inhibits the function of Bruton's tyrosine kinase (BTK), a key signaling molecule of the B-cell receptor signaling complex that plays an important role in the survival of malignant B cells. IMBRUVICA blocks signals that stimulate malignant B cells to grow and divide uncontrollably. Pharmacyclics added that IMBRUVICA is one of the first treatments to receive FDA approval via the Breakthrough Therapy Designation pathway and is commercially available now. 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.analystscorner.com/r/full_research_report/df74_PCYC

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