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BioCis Pharma Starts A Phase I Clinical Trial With A New Cancer Drug
BioCis Pharma Ltd., a privately-held drug development company with its headquarters in Turku, Finland, has started Phase I clinical testing of ProtoCure(TM) intravesical instillation solution, a novel anti-cancer drug for urinary bladder cancer. ProtoCure is based on a new mechanism of action discovered and developed by BioCis Pharma which effectively prevents cancer growth and proliferation locally.
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New Report Advises On How To Reduce Health Inequalities, UK
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Data Presented At Society Of Nuclear Medicine 2009 Annual Meeting Supports Potential Of Peregrine's Cotara(R) For The Treatment Of Brain Cancer
Peregrine Pharmaceuticals, Inc. (Nasdaq: PPHM) reported that researchers will present data at the SNM 2009 Annual Meeting showing that its brain cancer agent Cotara(R) specifically localizes to brain tumors at high concentrations with minimal radiation exposure to other organs. Cotara is a targeted monoclonal antibody linked to a radioisotope being developed as a potential new treatment for glioblastoma multiforme (GBM), a deadly form of brain cancer. The results reported from an ongoing dosimetry study at U.S. brain cancer centers show that in patients dosed in the first two cohorts of the study, the concentration of Cotara in brain tumors was on average more than 300-fold higher than in other normal organs. In addition, these patients have all either met or exceeded the expected median survival time of six months for recurrent GBM patients. Cotara is currently being tested in this Phase I dose response and dosimetry trial and in a Phase II clinical trial in recurrent GBM patients.
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SOS Research Project Assesses The Cardiovascular And Gastrointestinal Risk Related To The Use Of Non-steroidal Anti-inflammatory Drugs (NSAIDs)

Medical information of more than 35 million persons from the general European population will be studied with the goal of better guiding clinicians how to balance the risk of gastrointestinal and cardiovascular events when prescribing NSAIDs. NSAIDs are widely used in medical practice for treating pain, inflammation and degenerative joint diseases (for instance, arthritis). The use of traditional NSAIDs, however, is associated with an increased risk of minor and serious gastrointestinal events. It is estimated that in the European Union thousands of gastrointestinal complications are most likely caused by the use of NSAIDs every year. A new class of NSAIDs, the "Coxibs", has been developed specifically to minimize the risk of gastrointestinal events. Since their introduction, however, the use of these newer NSAIDs raised concerns since they may increase the risk of cardiovascular events, among which myocardial infarction and ischemic stroke. Here, the dilemma presents that the risk of gastrointestinal events has to be balanced against the risk of cardiovascular events. Both risks may differ in one single subject and for the 30 different NSAIDs that are available in the EU. Despite numerous evaluation studies several questions have yet remained unanswered, which hampers adequate treatment decision making around the use of individual NSAIDs. Single studies often are too small to look at all individual NSAIDs, mostly because only a particular set of NSAIDS is used in one country. Therefore we know very little on certain NSAIDs. By combining data from different countries, the heterogeneity and increased sample size are important for risk assessment and comparison of the different NSAIDs in subgroups such as adults and children. The SOS project aims to assess and compare the risk of cardiovascular and gastrointestinal events among NSAIDs users, with the ultimate goal to differentiate between NSAIDs and thereby providing decision models to clinicians and regulatory authorities, such as medicines agencies to guide the selection process of NSAIDs in clinical practice to minimize drug related harm. A thorough review of published literature of clinical trials and observational studies will be used to identify methodological issues and knowledge gaps which will be used to design and conduct a multi-country observational study. This study will include data from more than 35 million Europeans, extracted from existing health care databases in the UK, the Netherlands, Germany and Italy. These data will be used for multiple designs to generate knowledge which will be used to develop decision models to aid decisions in clinical practice on the type of NSAID that would yield the lowest gastrointestinal and cardiovascular risk for an individual patient. Decision models for regulatory agencies will focus on the public health risk. The SOS project (full title: "Safety Of non-Steroidal anti-inflammatory drugs") is funded with 2.8 million Euro granted by the European Commission in the 7th Framework Programme. SOS is coordinated by Professor Dr. Miriam Sturkenboom of Erasmus University Medical Center (Netherlands), and carried out by a consortium of 11 leading research institutions. EPCO


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