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Generic medicines pricing reforms deliver significant savings to Australian government, says CSES report

22 May 2013

Australia's 2010 Pharmaceutical Benefits Scheme (PBS) reforms have delivered the government significant savings. A report by Centre for Strategic Economic Studies, released this week, estimates that savings to government and general patients (non-health-card holding patients) will be up to A$18 billion ($17.53 billion) over eight years.

Sanofi and Regeneron's dupilumab shows 87% reduction in risk of asthma exacerbations

22 May 2013

French drug major Sanofi (Euronext: SAN) and US biotech partner Regeneron Pharmaceuticals (Nasdaq: REGN) announced that the New England Journal of Medicine published on-line the positive Phase IIa study results of dupilumab (SAR231893/REGN668) in patients with moderate-to-severe allergic asthma.

R-Pharm to invest 100 million euros in building a Turkish production plant

22 May 2013

R-Pharm, one of Russia's leading pharmaceutical producers, has officially announced the initiation of production of its drugs in Turkey and the possibility of establishment of its own manufacturing facility in the country.

NICE rejects Avastin for ovarian cancer, but backs Lucentis for RVO

22 May 2013

The UK's drugs watchdog the National Institute for Health and Care Excellence (NICE) has this morning (May 22) advised the National Health Service against funding the drug Avastin (bevacizumab) from Swiss drug major Roche (ROG: SIX) for advanced ovarian cancer. In two separate pieces of final guidance published for the health service, NICE concludes that funding the treatment on the NHS does not represent the best use of taxpayers' money.

AstraZeneca's naloxegol meets endpoints; EMA validates Gilead's sofosbuvir MAA

22 May 2013

Anglo-Swedish drug major AstraZeneca (LSE: AZN) yesterday (May 21) presented the results of two pivotal Phase III studies of naloxegol showing the 25mg dose of the investigational drug met its primary and secondary endpoints for efficacy and showed a safety profile consistent with previous studies for the treatment of opioid-induced constipation (OIC), at the Digestive Disease Week (DDW) meeting in Orlando, Florida, USA.

Biogen Idec files BLA for MS drug Plegridy in USA

21 May 2013

US biotech company Biogen Idec (Nasdaq: BIIB) has submitted a Biologics License Application (BLA) to the US Food and Drug Administration for approval of Plegridy (peginterferon beta-1a), the company's pegylated subcutaneous injectable candidate for relapsing forms of multiple sclerosis (RMS).

New Zealand declines Alexion's funding application for Solaris

21 May 2013

New Zealand's Pharmaceutical Management Agency PHARMAC is seeking feedback on a proposal to decline the application from USA-based drugmaker Alexion Pharmaceuticals (Nasdaq: ALXN) for funding its drug Solaris (eculizumab) for the treatment of paroxysmal nocturnal hemoglobinuria (PNH), a rare, acquired, potentially life-threatening disease of the blood.

Vectura fiscal 2012/13 revenues beat own expectations, and loss narrows

21 May 2013

UK inhaled therapies developer Vectura Group (LSE: VEC) yesterday presented its preliminary results for the year ended March 31, 2013, posting revenues slightly ahead of expectations at £30.5 million ($46.3 million), but down compared with £33 million in 2011/12.

CML drug revenue in Japan to grow, despite global decline, says GlobalData

21 May 2013

Bucking a global trend of falling revenues, weak penetration of generic drugs and an increasing patient population will ensure steady growth of Japan's Chronic Myeloid Leukemia (CML) market over the next decade, forecasts a new report from research and consulting firm GlobalData.

Novo A/S acquires Norway's Xellia Pharmaceuticals in $700 million deal

21 May 2013

Denmark-based Novo A/S, the holding company of the Novo Group and the major shareholder in Novo Nordisk and Novozymes, has purchased all shares of the Norwegian firm Xellia Pharmaceutical for around $700 million from 3i and other current shareholders. As a consequence of the transaction, Xellia will revert to Danish ownership with headquarters in Copenhagen.

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