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.
Looking at the genetics of bone marrow samples to see which genes affect resistance to treatment.
Assessing whether blocking a protein's activity could improve survival and reduce side effects.
Finding why immunotherapy doesn't work for some children with sarcoma tumours.
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.
Stopping protein activity to stop anaplastic large cell lymphomas from growing.
Looking at molecular makeup and MRIs to characterise infant ependymoma.
Developing a living systematic review of studies into new treatments for relapsed and refractory rhabdomyosarcoma.