Using existing drugs in a new way to treat high-risk acute lymphoblastic leukaemia
Finding drugs which target genes that drive high-risk acute lymphoblastic leukaemia.
We have been funding expert research since 2016, aiming to ensure that every child and young person has a safe and effective treatment for their cancer, and that they can live long and happy lives post-treatment.
Finding drugs which target genes that drive high-risk acute lymphoblastic leukaemia.
Creating antibodies in the lab to treat diffuse midline gliomas and testing their effectiveness.
Helping children in sub-Saharan Africa with endemic Burkitt Lymphoma get diagnosed earlier.
Understanding how proteins act inside acute myeloid leukaemia cells, to find new drug targets.
Assessing whether blocking a protein's activity could improve survival and reduce side effects.
Developing a living systematic review of studies into new treatments for relapsed and refractory rhabdomyosarcoma.
Looking into whether survivors of childhood cancer are at risk of severe infections.
Finding which regulatory regions of the genome are causing leukaemia by acting on the wrong gene
Developing more effective treatments for patients who have a low chance of survival, while reducing treatment and side effects for other patients.