Phase II open-label global study to evaluate the effect of dabrafenib in combination with trametinib in children and adolescent patients with BRAF V600 mutation positive Low Grade Glioma (LGG) or relapsed or refractory High Grade Glioma (HGG)
Study on Investigational Medications for Glioma with BRAF V600 Mutation
Brief description of study.
Detailed description of study
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Zanthiastrocytoma,Rosette-forming Glioneurona Tumor,Glioma,Astrocytoma,Iponeurocytoma,Gangliocytoma,High Grade Glioma,Glioblastoma,BRAF mutation,Papillary Glioneuronal Tumor,Oligodenroglioma,Low Grade Glioma,Neurocytoma
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Age: 1 years - 17 years
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Gender: All
Inclusion Criteria
Diagnosis of BRAF V600 mutant High Grade glioma that has relapsed, progressed or failed to respond to frontline therapy
Diagnosis of BRAF V600 mutant Low Grade glioma with progressive disease following surgical excision, or non-surgical candidates with necessity to begin first systemic treatment because of a risk of neurological impairment with progression.
Confirmed measurable disease
Exclusion Criteria
Previous treatment with dabrafenib, trametinib, other RAF inhibitor, other MEK or ERK inhibitor
HGG patient: Cancer treatment within the past 3 weeks.
LGG patient: Any systemic therapy or radiotherapy prior to enrollment
LGG patients: history of allergic reaction or contraindications to the use of carboplatin or vincristine
Stem cell transplant within the past 3 months
History of heart disease
Pregnant or lactating females
This study investigates the use of investigational medications in children and adolescents with a specific type of brain tumor called glioma. Glioma is a type of tumor that occurs in the brain and spinal cord. The study focuses on patients who have a BRAF V600 mutation, which is a change in the gene that can affect cell growth. The study is looking at two types of glioma: low grade glioma (LGG) and high grade glioma (HGG) that has come back or is not responding to treatment.
Participants in the study will receive either the investigational medications or a placebo. A placebo is an inactive substance that looks like the investigational medicine but does not contain any medicine. The study will assess the safety and effects of these treatments on the tumors.
- Who can participate: Children and adolescents with glioma and a BRAF V600 mutation can participate. They must have relapsed or unresponsive tumors or progressive disease, without prior similar treatments or recent cancer therapies.
- Study details: Participants will receive either the investigational medications or a placebo. The study will monitor the safety and effects of these treatments on the tumors.