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April 2012 Drug Information Update - Pharmacy Benefits ...

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a substantial improvement in their symptoms than those taking a drug-free placebo pill,<br />

regardless of how severe those symptoms were to begin with.<br />

Article link: http://www.reuters.com/article/<strong>2012</strong>/03/07/us-studyantidepressantsidUSTRE82623V<strong>2012</strong>0307<br />

Source website: http://www.reuters.com/<br />

Alexion drug offers hope for rare, deadly disorder<br />

March 7, <strong>2012</strong><br />

An experimental therapy for a rare, often fatal genetic disorder appears to offer hope for infants<br />

and very young children with the condition, according to data from a small clinical trial reported<br />

in the New England Journal of Medicine on Wednesday. The enzyme-replacement drug, asfotase<br />

alfa, acquired by Alexion Pharmaceuticals Inc with its $610 million purchase of Canada-based<br />

Enobia Pharma, could become the first approved treatment for the metabolic disease<br />

hypophosphatasia, or HPP.<br />

Article link: http://www.chicagotribune.com/health/sns-rt-us-alexionhypophosphatasiatre82621f-<strong>2012</strong>0307,0,7147932.story<br />

Source website: http://www.chicagotribune.com/<br />

Trial Shows Benefit in Using Prostate Cancer <strong>Drug</strong> Early<br />

March 8, <strong>2012</strong><br />

Johnson & Johnson said Thursday that its new drug for prostate cancer was effective when used<br />

earlier during treatment than it is now, potentially broadening its use and also posing a<br />

competitive threat to a rival drug, Dendreon’s Provenge. Johnson & Johnson’s drug, called<br />

Zytiga, was approved in <strong>April</strong> for use in men with advanced prostate cancer who had already<br />

tried chemotherapy using the drug docetaxel.<br />

Article link: http://www.nytimes.com/<strong>2012</strong>/03/09/business/trial-shows-benefit-in-earlier-useofzytiga-for-prostate-cancer.html?_r=2<br />

Source website: http://www.nytimes.com/<br />

Pfizer Calls Early End To Celebrex Safety Study In Children<br />

March 9, <strong>2012</strong><br />

Pfizer Inc. has terminated a long-term safety study of its blockbuster painkiller Celebrex in<br />

juvenile arthritis patients, citing difficulties in recruiting patients and a low rate of adverse<br />

events. New York-based Pfizer had agreed to conduct the study to address safety concerns in<br />

connection with the U.S. Food and <strong>Drug</strong> Administration's 2006 approval of the use of Celebrex<br />

to treat juvenile idiopathic arthritis. The FDA said at the time the use of Celebrex by adults<br />

suggested the possibility of longer-term cardiovascular problems.<br />

Article link: http://www.nasdaq.com/article/pfizer-calls-early-end-to-celebrex-safety-studyinchildren-<strong>2012</strong>0309-00729<br />

Source website: http://www.nasdaq.com/<br />

Leukemia No Longer a Death Sentence as 90% of Children Live<br />

March 12, <strong>2012</strong><br />

Childhood leukemia, once considered a death sentence, is now curable in nine out of 10 children,<br />

according to a study. Five-year survival rates for children diagnosed with acute lymphoblastic<br />

leukemia, the most common type in the young, rose to 90 percent in the years 2000 to 2005 from<br />

84 percent in 1990 to 1994, according to research today in the Journal of Clinical Oncology.<br />

16

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