Created in 2011 by a group of physicians and researchers, the International DIPG Registry collects information about DIPG patients and their tumors in order to help researchers ultimately find better treatments for them.

Medical Professionals

Learn more about DIPG, request a consultation, or contribute to our knowledge about the disease by referring a patient to the registry.

Enroll a Patient in the Registry (http://dipgregistry NULL.org/medical-professionals/enrollment/)

  • Request a Consultation (http://dipgregistry NULL.org/medical-professionals/consultation/)
  • Active Clinical Trials (http://dipgregistry NULL.org/medical-professionals/active-clinical-trials/)
  • Registry Research (http://dipgregistry NULL.org/registry-research/)

Patients & Families

Learn more about DIPG, including symptoms, current treatment approaches, and ongoing research. Request a second opinion or
learn about enrolling in the registry.

Get a Second Opinion (http://dipgregistry NULL.org/patients-families/second-opinion/)

  • Learn About DIPG (http://dipgregistry NULL.org/patients-families/basic-facts/)
  • Enroll in the Registry (http://dipgregistry NULL.org/patients-families/enrollment/)
  • Active Clinical Trials (http://dipgregistry NULL.org/patients-families/active-clinical-trials/)