Researchers Studying Oral Medication Combination After Radiation Therapy to Treat Patients With Newly Diagnosed High-Grade Glioma
Phase: Recruiting
First Posted: February
Condition(s): High-Grade Glioma
NCT Number: NCT03919071 Other Study ID Number(s): ACNS1723
What Is the Purpose of This Study?
To study how well the combination of dabrafenib and trametinib works after radiation therapy in children and young adults with high-grade glioma who have a genetic change called BRAF V600 mutation.
Who Can Take Part in This Study?
People who may be eligible for this study:
- Have newly diagnosed high-grade glioma (HGG) with BRAF V600 mutation, excluding metastatic disease.
- Patients can have BRAF V600 mutations with or without H3 K27M mutation (stratum 1 and 2 enroll patients without H3 K27M mutations and stratum 3 enrolls patients with H3 K27M mutations.
- Are 12 months to 21 years old.
For a full list of eligibility requirements, visit https://clinicaltrials.gov/study/NCT03919071
What Will Happen During This Study?
- Patients have local radiation 5 days a week for 6-7 weeks.
- Four weeks after radiation, patients will take two oral medications for 28 days in a row.