Avastin receives EU approval for the treatment of women with newly diagnosed, advanced ovarian cancer
Roche (SIX: RO, ROG; OTCQX: RHHBY) announced that the European Commission has approved Avastin (bevacizumab) in combination with standard chemotherapy (carboplatin and paclitaxel) as a front-line (first-line following surgery) treatment for women with advanced ovarian cancer. Ovarian cancer is the most deadly of the gynaecological cancers, with approximately 220,000 women diagnosed and 140,000 women dying from the disease each year globally.
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First-of-its-Kind Endovascular Trial of the Investigational Esprit(TM) Therapy
Abbott (NYSE: ABT) today announced the initiation of ESPRIT I, a first-of-its-kind clinical trial in Europe evaluating the safety and performance of the novel Esprit(TM) drug eluting bioresorbable vascular scaffold (BVS) for the treatment of blockages in the superficial femoral arteries (SFA) and iliac arteries that have resulted in claudication (leg pain upon walking). Claudication is the most common symptom in patients with peripheral artery disease (PAD), and is associated with diminished physical activity and poor quality of life for patients.
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Roche's personalized medicine Zelboraf receives positive opinion
Roche (SIX: RO, ROG; OTCQX: RHHBY), announced that the Committee for Medicinal Products for Human Use (CHMP) has recommended that Zelboraf be granted full marketing authorization as a monotherapy for the treatment of adult patients with BRAF V600 mutation-positive unresectable or metastatic melanoma. "The CHMP recommendation to approve Zelboraf represents an important milestone for people with metastatic melanoma who until recently had limited treatment options," said Hal Barron, M.D., chief medical officer and head, Global Product Development.
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Groundbreaking scientific collaboration gives UK academia access to compounds to advance medical research
A wide range of compounds will be made available free of charge to UK medical researchers next year, following a landmark agreement between the Medical Research Council (MRC) and AstraZeneca. In a new type of collaboration, academia will be granted access to 22 compounds, developed by AstraZeneca. Through MRC funding, UK academia will conduct studies to better understand what drives a range of diseases with a view to exploring new treatment opportunities.
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Boehringer Ingelheim gains approval of extended 4.5 hour time-window for Actilyse®
Boehringer Ingelheim announced that Actilyse® has been approved through a mutual recognition procedure for15 European countries* for thrombolytic treatment of acute ischaemic stroke up to 4.5 hours of onset of stroke symptoms and after prior exclusion of intracranial haemorrhage. This regulatory milestone was communicated by the reference member state Germany and will result in subsequent national approvals of the extended indication in the respective countries of the EU covered by the procedure. The national product informations will be amended accordingly.
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Novartis Foundation symposium looks at impact of Information and Communication Technology
Today a panel of experts in media, technology and healthcare are gathering to discuss the topic "New media - drivers of democratization and development?" at the 2011 Novartis Foundation for Sustainable Development (NFSD) symposium in Basel, Switzerland. They are exploring the ways that modern telecommunications technology has the power to transform the developing world - and how these technologies can specifically be harnessed to help improve access to healthcare.
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Boehringer Ingelheim and AVEO Pharmaceuticals announce manufacturing agreement for ficlatuzumab
AVEO Pharmaceuticals, Inc. (Nasdaq: AVEO) and Boehringer Ingelheim have entered into an agreement for large-scale process development and clinical manufacturing of ficlatuzumab, AVEO's novel HGF inhibitory antibody that is currently in phase II clinical development in patients with non-small cell lung cancer (NSCLC). Boehringer Ingelheim will produce ficlatuzumab for clinical trials at its biopharmaceutical site in Fremont, USA. AVEO retains all rights to the development and commercialization of ficlatuzumab.
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