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Experts Call On Colleagues To Drive Optimal Care For All Post-Mi Patients In The UK
Today experts from the Primary Care Cardiovascular Society (PCCS) and HEART UK - the Cholesterol Charity, are calling upon primary care clinicians to embrace new guidance designed to support optimal care and treatment of post-myocardial infarction (MI) patients. Published in the latest issue of the British Journal of Cardiology, the guidance is unique as it is aligned to both patients and primary care, thereby recognising the vital role of empowering patients and their families in achieving the best possible clinical outcomes.2

MedImmune Funds Study To Help Gain Insights Into Full Burden Of RSV Disease Among Premature Infants
MedImmune continues to advance its commitment to pediatric research with today"s announcement of the first observational prospective study designed to assess the burden of respiratory syncytial virus (RSV) among preterm infants 32-to-35 weeks gestational age (GA) in outpatient settings during their first year of life.
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UCB's Cimzia(R) Approved In The U.S. For Adult Patients Suffering From Moderate To Severe Rheumatoid Arthritis
Enzon Pharmaceuticals, Inc. (Nasdaq: ENZN) today announced that the U.S. Food and Drug Administration (FDA) has approved Cimzia®, for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA). Cimzia® (certolizumab pegol), is a PEGylated anti-TNFa (Tumor Necrosis Factor alpha). The product is currently being developed by UCB. Cimzia is one of several products which utilize Enzon"s PEGylation technology, including PEG-INTRON®, Macugen®, and Pegasys®.
Nutrition

AARP Biologics Study Based On Fuzzy Math, Flawed Assumptions

The following statement was issued by the Biotechnology Industry Organization (BIO) regarding a study on biosimilars presented to Congressional staff by the AARP: "The so-called AARP "study" is simplistic, misleading and extremely flawed. It is based on fuzzy math and even fuzzier assumptions. "The study cherry picks the best selling biologic products to draw erroneous conclusions, ignoring the bulk of the biologics market. The real facts show that only a small percentage of biotechnology products have the types of financial returns identified in the AARP study. If AARP had analyzed all of the more than 200 other FDA-approved biologics they conveniently left out of their fact sheet, their analysis would have reached a much different, and more credible, result. That"s because the "break even" point for all the other FDA-approved biologics approaches 50 years. "Greater than 90% of biologic products fail before even getting to clinical trials. Of those entering clinical trials, only 30% get approved by FDA. Of those approved products, only 34% generate profits equal to or greater than the development cost over the product"s lifecycle. "As one of the nation"s largest insurance providers, AARP has a lot to gain financially by using its considerable lobbying muscle to push Congress to pass biosimilars legislation that will benefit insurers by providing short-term cost savings at the risk of jeopardizing the continued development of advanced and breakthrough medicines and cures for patients. Biotechnology medicines extend and improve the quality of life - and provide renewed hope - for patients suffering from debilitating diseases such as cancer, HIV/AIDS, Parkinson"s, Multiple Sclerosis, diabetes and a host of rare diseases. "Congress should not develop public policy based on such a flawed and blatantly biased analysis. Now is the time to implement a pathway to biosimilars that safely increases access to the breakthrough therapies and cures for the patients of today, while preserving the incentives necessary to address the unmet medical needs of the patients of tomorrow." BIO


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