Roche subsidiary Genentech has been granted FDA breakthrough therapy designation for its ACE910 (RG6013, RO5534262) haemophilia A therapy. The designation …

Several treatments that extend the lives of people with cancer are expected to be removed from the Cancer Drugs Fund …

The European Commission has approved Novartis’s Farydak, in combination with Velcade and dexamethasone, for the treatment of adult patients with …

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Novartis has won the investigational heart failure treatment LCZ696 (sacubitril valsartan) will be available in the UK under the Early …

UK health ministers have challenged the NHS to fully utilise technology, to empower patients to manage their own healthcare needs.Their …

The US Defense Advanced Research Projects Agency (DARPA)’s $45 million ‘Big Mechanism’ initiative has an ambitious aim.It promises to “leapfrog …
NICE has published final draft guidance confirming its recommended treatment options for rheumatoid arthritis. For the first time copycat, or …

Sandoz, the generics arm of the pharma giants Novartis, has become the first company to launch a biosimilar product in …

Shire has appointed Sara Mathew to its board of directors as a non-executive director.Mathew will also be a member of …

The pharma industry has excessive power over EU decision-makers and spends €40 million a year to influence EU drug policy, …

Amgen and Novartis have announced a global collaboration to develop neuroscience treatments in Alzheimer’s disease and migraine. The companies plan …

The European Commission has approved Revolade for severe aplastic anaemia, and the combination of Tafinlar and Mekinist for patients with …

Around 96 in every 100 people treated with Bayer’s anticoagulant Xarelto do not experience any major bleeding, related side effects …

Google is continuing its work in diabetes, by teaming up with pharma giants Sanofi to create new digital technologies and …

Over the past decade, pharmaceutical companies and regulatory agencies have been reviewing the benefit-risk assessment of medicines with a view …

Two treatments developed by ultra-rare disease specialists Alexion Pharmaceuticals are now approved for use in Europe. The European Commission approved …

Bristol-Myers Squibb is flexing its muscles in respiratory disease, by signing a deal to acquire the exclusive right to acquire …

The FDA has issued a safety alert, warning of joint pain caused by the gliptins, a common class of drugs …

Clinical technology and services company Mytrus has announced that its software platform for electronic informed consent has received approval for …