Interim data from the Phase IIIb STARDUST study showed that 79% of patients with moderately to severely active Crohn’s disease (CD) achieved clinical response and 67% were in clinical remission.
Interim data from the Phase IIIb STARDUST study showed that 79% of patients with moderately to severely active Crohn’s disease (CD) achieved clinical response and 67% were in clinical remission.
Many of the cases in 2019 were seen in the so-called ‘Wakefield cohorts’ – young adults born in the late nineties and early 2000s who missed out on the MMR vaccine when they were children.
Ensifentrine showed clinically and statistically significant improvements in lung function at all doses.
The device has potential to save the NHS around £6,200 per patient assuming a 15-year life span.
A “lack of skills and a distrust of health information online” are two of the biggest barriers keeping patients from using the internet.
Earlier this week, NICE released a draft guidance rejecting Keytruda when used in combo with Pfizer’s Inlyta (axitinib) to treat advanced renal cell carcinoma.
Earlier this month, Roche also announced a gantenerumab Alzheimer’s failure, and last year Biogen and Eisai stopped two global Phase III trials of aducanumab.
The GenesisCare technology is part of a £20m investment.
More than nine out of every 10 lung cells in current smokers have up to 10,000 extra genetic changes compared to non-smokers.
If approved, it will become the first therapy to specifically target METex14 mutated advanced lung cancer, a type of lung cancer with a particularly poor prognosis.
Despite evidence suggesting that the Keytruda combo would be welcomed by patients, NICE cites uncertainty around the long-term benefit.
The company will also make the UK the global centre of a major new clinical trial to investigate the use of inclisiran in improving cardiovascular outcomes.
The 2020 competition will be closing for entry in just a months time on the 13th March.
Despite the recent approval of some high-profile nucleic acid therapy drugs, success has been modest, and there is still a “huge burden” of unmet medical need due to the vast number of diseases that are untreatable with traditional therapies.
The EMA also recently validated a Marketing Authorisation Application for the drug.