Following weeks of speculation Pfizer has stepped forward with a $14-billion bid for Medivation, beating Sanofi and other suitors to the finish line in a move designed to boost its oncology portfolio.
Following weeks of speculation Pfizer has stepped forward with a $14-billion bid for Medivation, beating Sanofi and other suitors to the finish line in a move designed to boost its oncology portfolio.
The European Commission has issued a green light for Teva’s Cinqaero in the 28 countries of the European Union in addition to Norway, Liechtenstein and Iceland.
Pfizer’s Troxyca ER has been approved in the US for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate.
The group is seeking conditional approval for the drug’s use when reversal of anticoagulation is needed due to life-threatening or uncontrolled bleeding and for patients requiring urgent or emergency surgery.
NHS England has revealed that £365 million will be streamed into specialist perinatal mental health services over the next five years to increase access to care and treatment.
Bayer’s Nexavar is the latest medicine currently available through the Cancer Drugs Fund that has failed to meet cost-effectiveness standards set by the National Institute for Health and Care Excellence.
Janssen Biotech is seeking to expand the scope of Darzalex as a second-line combination treatment for multiple myeloma.
A “groundbreaking” new app designed to help healthcare staff tackle antibiotic resistance has been launched in Scotland.
Hospital deaths from the most common form of pneumonia dropped 14 percent between 2009 and 2015, according to new research published online in Thorax, the journal of the British Thoracic Society (BTS)
The government has let down future generations with a watered-down strategy that will fail to adequately tackle the rising swell of obesity in the country, campaigners say.
Merck & Co is reportedly the latest pharma to consider snapping up US cancer biotech Medivation.
Portola has been dealt a blow after its anticoagulation reversal drug AndexXa was rejected by the US Food and Drug Administration.
The Association of the British Pharmaceutical Industry and the National Centre for the Replacement, Refinement, and Reduction of Animals in Research (NC3Rs) have announced a new collaboration to explore whether the safety testing of medicines can be refined.
Patients with breast cancer and mantle cell lymphoma living in England and Wales have been dealt a blow after cost regulators rejected two drugs currently available through the Cancer Drugs Fund for routine NHS use.
The Royal National Institute for the Blind claims that its research continues to show cataract operations are being restricted due to financial pressures on the NHS.