News

Boehringer links with Dundee Uni in PROTAC deal

Boehringer links with Dundee Uni in PROTAC deal

Boehringer Ingelheim and Dundee University have joined forces to develop a novel class of medicines that target disease causing proteins for degradation and address areas where there remains unmet need.

GSK licenses respiratory disease target from Five Prime

GSK licenses respiratory disease target from Five Prime

GSK has exercised its option for an exclusive license to a respiratory disease target identified through its research collaboration with Five Prime Therapeutics, triggering a $1.5 million milestone payment to the US biotech.

NHS spends £780,000 a day on antidepressants

NHS spends £780,000 a day on antidepressants

The National Health Service in England is now shelling out £780,000 a day on antidepressants which, out of all BNF drug categories, saw the greatest numeric rise in prescriptions in 2015.

Wales confirms £80m treatment fund

Wales confirms £80m treatment fund

A new £80 million fund designed to help accelerate access to treatments for patients with life-threatening illnesses in Wales has now been confirmed by the Welsh government.

Sepsis as serious as heart attack, says NICE

Sepsis as serious as heart attack, says NICE

UK healthcare workers have been told to treat patients with suspected sepsis with the same urgency as those with suspected heart attack, in new guidelines from the National Institute for Health and Care Excellence.

NICE to expand reach of RA drug Cimzia

NICE to expand reach of RA drug Cimzia

NICE has published draft guidance recommending UCB Pharma’s TNF inhibitor Cimzia as an option for severe rheumatoid arthritis when other drugs haven’t worked or aren’t suitable.

HIV transmission risk slashed with antiretroviral therapy

HIV transmission risk slashed with antiretroviral therapy

Findings of the PARTNER study, the world’s largest study of people with HIV who have had condomless sex with their HIV-negative partners, lend further weight to the use of antiretroviral therapy as a means of preventing infection with the virus.

FDA expands use of Pfizer’s Prevnar

FDA expands use of Pfizer’s Prevnar

US regulators have expanded the scope of Pfizer’s pneumococcal vaccine Prevnar 13, allowing its use in adults aged 18 to 49 years of age.

Amgen’s Humira biosimilar backed by FDA panel

Amgen’s Humira biosimilar backed by FDA panel

A US Food and Drug Administration’s advisory committee is supporting the approval of Amgen’s biosimilar of AbbVie’s biologic Humira, the world second best-selling drug.