Researchers Studying Oral Medicine During and After Radiation to Treat Newly Diagnosed DIPG and HGG

Phase: Recruiting

First Posted: January

Condition(s): Diffuse Intrinsic Pontine Glioma (DIPG), High-Grade Gliomas (HGG)

NCT Number: NCT01407744 Other Study ID Number(s): ACNS1821

What Is the Purpose of This Study?

To test the safety, side effects, and best dose of an oral medicine given in combination with standard radiation therapy to treat children and young adults with newly diagnosed diffuse intrinsic pontine glioma (DIPG) or high-grade glioma (HGG) with a genetic change called H3 K27M mutation.

Who Can Take Part in This Study?

People who may be eligible for this study:

  • Are newly diagnosed with diffuse intrinsic pontine glioma (DIPG) or high-grade glioma (HGG) with a genetic change called H3 K27M mutation.
  • Are 1 to 21 years old.

For a full list of eligibility requirements, visit https://www.clinicaltrials.gov/study/NCT01407744

What Will Happen During This Study?

  • An oral medicine will be given once weekly for 8 weeks concurrently with radiation therapy for the first 5-7 weeks.
  • Patients will take medicine for up to 24 cycles. Each cycle lasts 4 weeks.

Principal Investigator

Mark A. Ranalli
MD

Hematology & Oncology

Discover More Research
Explore additional studies relating to neuro-oncology