This international, multicentre study is evaluating the combination of tovorafenib and vinblastine in children and young adults aged 25 and younger who have recurrent or progressive low-grade glioma (LGG) with specific genetic alterations, including types of CRAF or BRAF mutations and fusions.
The study aims to assess the safety, feasibility and effectiveness of tovorafenib and vinblastine for treating this group of patients. The treatment will be given for up to 24 months.
VICTORY is an international multicentre pilot study to investigate the safety and efficacy of Vinblastine with Tovorafenib in paediatric and young adult patients with recurrent or progressive RAF altered (non-NF1) LGG. The study will occur in two phases; Phase A focuses on dose finding and feasibility, while Phase B assesses overall efficacy. The primary objective is to determine the maximum tolerated dose (MTD/RP2D) of combination of vinblastine + tovorafenib, and to determine overall response rate of CR, PR and MR in patients with LGG treated with combination of vinblastine + tovorafenib by RANO-LGG criteria.