People with motor neurone disease (MND) are set to benefit from improved collaboration between the government, researchers and charities, on top of accelerated access to funding, to speed up progress into developing treatments and finding a cure.
The Health and Social Care Secretary, Steve Barclay, met with leading representatives from across the MND research community yesterday, including a number of medical research charities, to discuss ways to fast-track research into the disease and look at how the government and sector can work better together to benefit patients.
MND continues to have a devastating impact on the lives of people living with the condition and their families. The roundtable set out how the government will continue to work closely with the research sector, cut red tape to make accessing funding easier and boost research into new treatments.
Following the roundtable, the Health and Social Care Secretary visited the King’s College Hospital MND Care and Research Centre to meet staff, patients and charities to see first-hand how government funding for MND research has benefitted them. King’s research labs helped find the only current treatment that targets the underlying causes of neurological diseases such as MND, and is aiming to find a cure and improve quality of life for patients and their families.
The NHS App has also now been updated to make it easier for people to take part in MND and wider health research. People will be able to visit Be Part of Research through the app to view and sign up to research.
Health and Social Care Secretary Steve Barclay said: "Motor neurone disease can have a devastating impact on people’s lives, and I’m working with leading researchers to accelerate research and help find a cure as soon as we can. We have made strong progress since we pledged £50 million for MNDresearch with new treatments being developed and promising results from clinical trials reported, but I know there is still more to do. Yesterday, I held a roundtable with experts, charities and patients to discuss how we can encourage and invest in the best research to drive more results.
"By cutting red tape and building on existing investments, we are making sure funding gets to researchers as quickly as possible. I encourage people in England to sign up to research via the NHS App and join our ever-growing UK-wide register Be Part of Research."
There are many different types of research users of the NHS App can sign up to, including studies that test new treatments via interviews or surveys. A study might take place in a hospital, GP practice, or other health and social care locations in the community but some studies can also be done at home, online or by telephone.
For example, dentist and former football manager Dean Mooney, whose life has changed dramatically since his amyotrophic lateral sclerosis (ALS) diagnosis, has appealed to others who have the disease to join him in a new brain imaging study to help the race to find new treatments. Dean has worked with the University of Exeter’s world-leading Neurodegeneration Imaging Group, led by Professor Marios Politis, that is appealing for people who have MND to get in touch, and take part in a year-long study.
Since the government cut red tape in December to speed up £50 million into MND research across the UK, immediate investment of £29.5 million was injected through specialist research centres so NHS patients could benefit from cutting-edge treatment and medicines. There are more clinical trials than ever before, delivering promising developments, such as research from NIHR’s Sheffield Biomedical Research Centre into the drug Tofersen, with findings suggesting it may slow progression of the disease for some people living with MND.
There have also been applications proposing a collaboration between researchers to establish a clinical trial in new medicines and building infrastructure to support MND research activity in laboratories. In addition, discussions are underway with the sector to develop a proposal for an additional £2 million to focus on analysing existing data on the condition to explore the underlying causes of MND and help develop breakthrough new treatments as part of the MND Collaborative Partnership.
CEO of the NIHR Professor Lucy Chappell said: "We are working hard to accelerate progress in motor neurone disease research. The charities and campaigners have done so much to focus attention and government is committed to delivering resources. This roundtable is a great opportunity to bring patient groups, world-leading experts, and government research funders together. We need to work together to ensure that high quality research is funded, so breakthroughs can reach patients as quickly as possible.
"MND patients have shown the value to us all of taking part in research and I am excited that we are now making it even easier for people in England to register their interest in research via the NHS App and Be Part of Research."
The remainder of the £50 million MND funding is available for researchers to access via the National Institute for Health and Care Research (NIHR) and Medical Research Council (MRC) who are working together to ensure proposals are referred to the most appropriate scheme for consideration at the early idea stage.
