News

Final NICE nod for dry eye drug

Cost regulators for the NHS in England and Wales have now issued final guidelines permitting routine use of Santen’s Ikervis to treat severe keratitis in adults with dry eye disease which has not improved despite treatment with artificial tears.

Final NICE OK for Biomarin’s Vimizim

Patients with a very rare inherited lysosomal storage disease will now get treatment with Biomarin’s Vimizim funded on the National Health Service in England and Wales after cost regulators issued a final nod for the drug.

First Clinical Commissioning Group in special measures

In an unprecedented move, NHS England has now placed NHS Shropshire Clinical Commissioning Group in special measures, indicating that it has grave concerns across the breadth of the Group’s operations. 

GSK/Janssen RA drug on track for filing next year

A new therapy being developed by GlaxoSmithKline and Janssen as a treatment for rheumatoid arthritis has passed late-stage clinical safety and efficacy tests, paving the way for regulatory filings next year.

Amgen takes back three drugs from GSK

Amgen has entered into a definitive agreement with GSK to reacquire all of its remaining rights to bone drugs Prolia (denosumab) and Xgeva (denosumab) and cancer therapy Vectibix (panitumumab) in 48 countries around the globe.

Women missing out on cardiac rehab

More than 24,000 female heart patients are missing out on crucial rehabilitation, putting thousands at greater risk from further heart attacks, finds a new report from the British Heart Foundation.

AZ confirms talks with Acerta Pharma

AstraZeneca has confirmed that it is in talks to buy privately held US/Dutch clinical stage biopharma Acerta Pharma, in a deal speculated to be worth around $5 billion.

Accelerated approval for Roche’s lung cancer drug

Roche group Genentech’s Alecensa has been given a speedy US approval for a particular type of non-small cell lung cancer (NSCLC), giving patients access to a new targeted treatment option.