New Online Resource Launches For Patients With Chronic Myeloid Leukemia
Many people living with cancer are researching their illnesses online. In fact, research has shown that patients who use the Internet consider it a more useful source of information as compared with other media. Further, patients' Internet use can encourage active communication with their physicians. These are the reasons why, Bristol-Myers Squibb Company (NYSE:BMY) is making available a new comprehensive Web site called MyCMLCare.com for patients with chronic myeloid leukemia (CML) and their caregivers.
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European Commission approves statement on lipid improvement for Viramune® label
Boehringer Ingelheim announced that the European Commission has approved an update of the Summary of Product Characteristics (SmPC) for Viramune® (nevirapine) in the treatment of patients with HIV. The decision followed a positive recommendation by the Committee for Medical Products for Human Use (CHMP), the scientific committee of the European Medicines Agency (EMEA) who reviewed the clinical evidence and approved a statement in the SmPC recognising the positive effect of nevirapine on the lipid profile of HIV infected patients.
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Schering-Plough Announces Phase II and III Data for Corifollitropin Alfa
Schering-Plough Corp., (NYSE: SGP) has announced results from the Phase III ENGAGE clinical trial demonstrating that a single injection of corifollitropin alfa, first in the class of sustained follicle stimulants, achieved similar efficacy to recombinant follicle stimulating hormone (rFSH) given once daily for seven days.
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IRESSA (Gefitinib) Receives Marketing Authorisation in Europe
AstraZeneca announced that the European Commission has granted marketing authorisation for the oral anti-cancer drug, IRESSA for the treatment of adults with locally advanced or metastatic non-small cell lung cancer (NSCLC) with activating mutations of EGFR-TK (epidermal growth factor receptor-tyrosine kinase) across all lines of therapy.
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Once-yearly Aclasta® approved in EU to treat osteoporosis
Steroids, widely used to treat inflammatory conditions, can cause bone loss and increase risk of fractures in up to 50% of patients on long-term therapy[1]
European approval based on data showing Aclasta better at increasing bone mass than oral risedronate, a current established therapy[2],[3]
Clinical trial results also reaffirm efficacy and safety of Aclasta, used in more than 500,000 patients worldwide since launch in 2007[4],[5]
Approval is fifth indication for once-yearly Aclasta, already approved worldwide to treat postmenopausal osteoporosis[6]
ONGLYZA (saxagliptin) Receives Positive Opinion in Europe for the Treatment of Type 2 Diabetes
AstraZeneca and Bristol-Myers Squibb Company today announced that their marketing authorisation application for ONGLYZA (saxagliptin) received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) for the treatment of type 2 diabetes in adults as add-on therapy with metformin, a thiazolidinedione or a sulphonylurea.
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GSK and Chroma Therapeutics form alliance to develop novel macrophage-targeted drugs
GlaxoSmithKline (LSE: GSK) and Chroma Therapeutics Limited announced a collaboration to develop macrophage-targeted compounds using Chroma's proprietary esterase-sensitive motif (ESM) technology, which adds amino acid esters to compounds with the aim of targeting the compounds to specific cells in the inflammatory disease process.
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