The combo has been granted Accelerated Approval in the US.
The combo has been granted Accelerated Approval in the US.
MedDay will review the latest findings in detail “to understand these outcomes to help inform future clinical research in progressive MS and other neurological diseases.”
The rejection comes after a review of new evidence collected while the blockbuster was available via the Cancer Drugs Fund.
As well as testing of people who meet the criteria for being at risk, the NHS and PHE are also carrying out surveillance testing on people in wards and surgeries showing signs of the virus.
BMS is “disappointed” at the outcome.
In a trial, the addition of DE-122 to Roche’s Lucentis (ranibizumab) did not improve visual acuity compared to treatment with Lucentis alone.
The two organisations have detailed plans to work together on planning and information sharing over the assessment of medical technologies.
Picking out patients whose cancers have high-risk genetic features could help clinicians realise sooner if they’re unlikely to respond to treatment, enabling them to find alternative options as early as possible.
The 2020 Clinical Researcher of the Year – The Americas competition will be closing for entry at midnight this Friday the 13th March.
The drug is the first licensed treatment available on the NHS in the UK to treat this condition.
The discovery could be the answer to why some people are more likely to develop a devastating lung disease – idiopathic pulmonary fibrosis (IPF).
Since 2015, the first-of-its-kind collaboration has brought together academic and pharmaceutical industry researchers to create a deeper understanding of how HIV works.
Find out which individuals and teams will be putting their skills to the test in the live finals days later this year.
The novel mammography imaging system could potentially “spell an end” to unnecessary biopsies, by determining benign or malignant breast lesions.
The authorisation shortens the treatment period from from 12 to eight weeks.