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.
Helping children in sub-Saharan Africa with endemic Burkitt Lymphoma get diagnosed earlier.
Looking at molecular makeup and MRIs to characterise infant ependymoma.
Creating antibodies in the lab to treat diffuse midline gliomas and testing their effectiveness.
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.
Developing better models of rhabdomyosarcoma to test available treatments.
Developing more effective treatments for patients who have a low chance of survival, while reducing treatment and side effects for other patients.