The BTD is for the treatment of paediatric patients aged three years and older with neurofibromatosis type 1 (NF1).
The BTD is for the treatment of paediatric patients aged three years and older with neurofibromatosis type 1 (NF1).
The approval is based on data from three Phase III studies, ACLIFORM, AUGMENT and AMPLIFY.
The number dispensed last year was almost double the 36 million recorded a decade ago in 2008.
The drug is the first oral MS treatment to provide two years of proven efficacy with a maximum of 20 days of treatment.
The Swiss company will pay $310 million in upfront payments.
The FDA has approved the drug for a certain type of inflammatory arthritis called non-radiographic axial spondyloarthritis.
The ABPI has warned that “there a range of things outside of our control”.
The European Medicines Agency’s CHMP positive opinions are sparse this time around.
If approved, the drug will be the only therapy in nearly 20 years to reduce the risk of end-stage kidney disease.
The study found that patients warned of adverse consequences to their own health of skipping doses were more likely to adhere.
The CE-marked prognostic test for guiding treatment options uses a gene expression “signature”.
The partnership will give the American pharma giant access to Concerto’s eurekaHealth AI insights platform.
The collaboration is aligned with AstraZeneca’s science-led strategy in oncology.
The Trinity College spin-off has completed a £1.5-million funding round for its autoimmune treatments.
The social prescription plan aims to bring about the major shift in perspective needed.