For many years, people living with brain tumours have faced inequalities in research and treatment. Compared with more common cancers, research investment is limited, clinical trials are harder to access and new treatments can take longer to reach patients. This law represents a significant step towards closing that gap.
The Rare Cancers Bill is designed to transform how rare cancers are supported in the UK including:
One of the biggest challenges for rare cancer patients has been finding and joining relevant research studies. This legislation will help make patient data more accessible for research purposes and improve the way eligible patients are identified and contacted about trials.
The new law will make it the Government’s duty to promote and facilitate research into rare cancers, including many types of brain tumours.
Appointment of a National Specialty Lead for Rare Cancers, a dedicated role within the National Institute for Health and Care Research (NIHR), responsible for accelerating research and improving access into clinical trails.
“Orphan drugs” are drugs designed to treat rare conditions, but historically they were perceived as non-commercially viable. The new law will set out a formal review of the UK’s regulatory framework for orphan drugs, to enable innovative treatments to be developed and approved for use.
The Bill’s passage is a testament to years of campaigning by charities, patients, clinicians, and advocates who have worked to raise awareness of the unique challenges faced by individuals impacted by a brain tumour. While this is a huge step forward, legislation is only the start. Progress will depend on how this law is put into action, how research funding and implementation follow through and how quickly patients can see improvements in trial access and treatment options.
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