News

NICE U-turn backs biologics for ulcerative colitis

The National Institute for Health and Care Excellence has reversed a previous guidance and recommended use on the NHS of three big-selling biologics – Merck & Co’s Remicade and Simponi and AbbVie’s Humira – for treating moderately to severely active ulcerative colitis.

Action urged now cancer is UK’s most common cause of death

Last year, cancer was the most common cause of death for men and women in the UK, replacing circulatory diseases including heart disease and stroke, which were the nation’s most common cause of death until 2010, say government figures.

Agios first-in-class drug looks effective for AML

A small but significant study of Agios Pharmaceuticals’ AG-221, partnered with Celgene, caused a stir at the American Society of Hematology meeting in San Francisco earlier this week.

Celgene ends stellar week with positive Abraxane data

After a highly successful American Society of Hematology meeting in San Francisco earlier this week, Celgene has been further boosted by positive data for Abraxane at the San Antonio Breast Cancer Symposium.

Teva sees generic Copaxone competition on horizon

Foreign exchange rates and generic competition for its multiple sclerosis blockbuster Copaxone has led Teva Pharmaceutical Industries to making 2015  forecasts below analysts’ expectations.

USA looks at new antibiotics approval pathway

As superbugs return to the spotlight, US Senators Michael Bennet and Orrin Hatch have introduced a bill to create a new drug approval pathway “to streamline access and encourage innovation and development” of antibiotics.

50% of women in England taking prescribed drugs

43% of men and 50% of women in England have told a government survey that they had taken at least one prescribed medicine in the last week, and 22% of men and 24% of women reported that they had taken at least three prescribed drugs during the period.

Cancer Drug Fund needs ‘more radical’ changes, say experts

Proposed new arrangements for prioritising access to the Cancer Drug Fund “will continue to undermine NICE, duplicate effort and distort allocation of NHS resources, while failing to support the development of cost-effective drugs from which patients will benefit,” says a team of leading health economists.

FDA approves new version of Merck & Co’s Gardasil

The US Food and Drug Administration has approved Merck & Co’s new version of Gardasil which protects against an additional five strains of the human papillomavirus that causes most cases of cervical cancer.