News

NICE says ‘no’ to personalised bowel cancer drugs

The National Institute for Health and Care Excellence has published interim guidance barring patients with advanced bowel cancer from routine NHS access to Merck Serono’s Erbitux and Amgen’s Vectibix, the only two personalised options still available for the disease.

FDA speedy review for BMS’ Opdivo in kidney cancer

US regulators are undertaking a priority review of Bristol-Myers Squibb’s immunotherapy Opdivo for the treatment of patients with advanced renal cell carcinoma, the most common form of kidney cancer which kills more than 100,000 people every year.

Monitor consults on first ever NHS whistle-blowing policy

UK regulators have unveiled plans for the first ever National Health Service whistle-blowing policy to encourage and support those wishing to ring alarm bells over poor quality care, after a line of safety scandals in which patient harm could have been avoided if staff concerns had been listened to and addressed.

Roche’s Kadcyla too expensive for NHS, says NICE

Breast cancer patients and campaigners will be hugely disappointed with news this morning that Roche’s Kadcyla will not be routinely available on the National Health Service in England and Wales.

FDA nod for Baxalta’s long-acting haemophilia drug

The US Food and Drug Administration has approved Baxalta’s long-acting haemophilia drug Adynovate for both treatment and prevention of bleeding episodes in adults and adolescents with Haemophilia A.

MSD’s hep C combo cures 90% of patients with liver cirrhosis

MSD’s once-daily, single pill, fixed-combination therapy elbasvir/grazoprevir is causing a stir after an analysis of trial data showed that it was able to cure the vast majority of hepatitis C patients who also had compensated liver cirrhosis, a traditionally difficult-to-treat population.

Speedy US OK for AZ’ targeted lung cancer therapy

US-based patients with a particular form of lung cancer could now get access to the first targeted therapy for their condition, after the country’s Food and Drug Administration issued accelerated clearance for AstraZeneca’s Tagrisso (formerly AZD9291).

US expands scope of Gilead’s Harvoni

The US Food and Drug Administration has expanded the scope of Harvoni allowing its use in patients with genotype 4, 5 and 6 chronic hepatitis C virus infection and in those co-infected with HIV.

BMA unveils planned dates for industrial action

In an unusual move, the British Medical Association has unveiled three dates in December for planned industrial action by junior doctors in England ahead of the outcome of its current ballot, which closes next week.