The UK’s Medicines and Healthcare products Regulatory Agency is linking hands with its counterpart in India in a move designed to boost public safety in both nations.
The UK’s Medicines and Healthcare products Regulatory Agency is linking hands with its counterpart in India in a move designed to boost public safety in both nations.
The US Food and Administration has cleared a new treatment approach for pulmonary arterial hypertension which combines Gilead’s Letairis and Lilly’s tadalafil to magnify the benefits offered by each therapy alone.
UK drugmaker Vernalis has bought US rights to the long-acting antibiotic Moxatag, the first and only approved once-daily formulation of amoxicillin, further strengthening its foothold across the pond.
US regulators have widened the scope of Merck & Co’s immunotherapy Keytruda to include the treatment of certain patients with lung cancer.
Israeli drugmaker Teva is buying Mexican drugmaker Rimsa for $2.3 billion, expanding its presence in one of the world’s top five emerging markets.
Novartis has licensed a potential first-in-class immuno-oncology programme from XOMA in a deal potentially worth more than $500 million, sending the latter’s shares up nearly 50%.
The FDA has accepted Novartis’ submission for its biosimilar of Amgen’s Enbrel, which could mark the second time Amgen sees biosimilar competition from the Swiss company.
Private US biotech Berg is bringing its artificial intelligence technology to the UK’s 100,000 Genomes Project, in order to help analyse massive datasets relating to patients and cell biology.
US regulators have approved the first combination of two immuno-oncology agents – Bristol-Myers Squibb’s Opdivo and Yervoy – to treat certain patients with advanced skin cancer.
General practice will cost the National Health Service £1.2 billion a year by 2025 because of an “explosion” of people living with long-term conditions, the Royal College of General Practitioners has warned.
A survey of 551 GPs in England has revealed a growing divide between GPs and pharma, with two-thirds no longer meeting with sales representatives and more than 40% having a negative perception of the industry.
GlaxoSmithKline has exercised an option to license inhaled therapeutics created via a particle manipulating technology developed by University of North Carolina spinout Liquidia Technologies, under a pre-existing collaboration between the firms dating back to 2012.
Merck Serono has reversed its deal with BioMarin for the rights to Kuvan and Peg-Pal as it seeks to strengthen its focus on its core businesses.
The National Health Service is working with firefighters under a new partnership that seeks to address potential health and social issues at an earlier stage, in order to help people live longer, more independent lives and reduce winter pressures on care systems.
UK charity Breast Cancer Now is petitioning Roche to cut the price of its breast cancer drug Kadcyla – temporarily at least – so that it can remain available to patients in England through the Cancer Drugs Fund.