News

Sandoz files Enbrel biosimilar in the EU

European regulators have accepted Sandoz’ marketing application for a biosimilar of Pfizer’s $9-billion-a-year anti-inflammatory Enbrel, the world’s fifth biggest selling drug.

FDA clears Alexion’s enzyme replacement therapy Kanuma

US regulators have issued a green light for Alexion’s long-term enzyme replacement therapy Kanuma, giving patients with the ultra rare genetic disorder lysosomal acid lipase deficiency access to a targeted treatment for the first time.

Five medicines cleared for use by NHS Scotland

Five medicines have been accepted by cost regulators for routine use on the NHS in Scotland, offering patients access to new options for lung cancer, multiple myeloma, opioid-induced constipation and the chronic skin condition rosacea. 

Amgen files Humira biosimilar in EU, signs Merck deal

Amgen has filed the first biosimilar version of AbbVie’s anti-inflammatory super-blockbuster Humira in the European Union, in the hope of offering a cheaper alternative to the drug and thus potentially improving access to it.

Charity calls on NICE to reverse rejection of Amgen’s PCSK9 inhibitor

Cholesterol charity HEART UK is calling on NICE to reverse its rejection of Amgen’s cholesterol-busting drug Repatha for use on the National Health Service in England and Wales, slamming the move for leaving high-risk patients in danger of suffering heart attack or stroke.

GPs prescribing fewer antibiotics score less on patient satisfaction

Researchers from King’s College London have found that GPs dishing out fewer antibiotics are rating lower on patient satisfaction, indicating that a significant shift in public perception is still needed to help curb their use and pull back the rise of antimicrobial resistance.

Lilly, Merck drop late-stage diabetes, cancer drugs

Pharmaceutical giants Lilly and Merck KGaA have taken a hit to their late-stage research and development pipelines with the failure of their respective experimental drugs for diabetes and cancer.