Hodgkin Disease Registry

What we are studying

This study is a registry (a collection of information to help study Hodgkin disease) and collection study designed to allow us to better understand why some people get Hodgkin Disease, how different people respond to therapy and how to look for problems caused by the treatment. The goal of this study is to collect and distribute samples obtained from subjects with Hodgkin Disease.

Who is Eligible

  • Genders:
    • Men
    • Women
  • Races:
    • White
    • African American
    • Asian
    • American Indian or Alaska Native
    • Native Hawaiian or Pacific Islander
    • Other
  • All Ethnicities
  • All Ages up to 22

Eligibility Criteria

  • Newly diagnosed untreated Hodgkin Disease

What is involved

  • You are going to have a biopsy (or surgery) to see if you have cancer.
  • Your doctor will remove some tissue to make the diagnosis of your disease. This is not research. The results of these tests will be given to you by your study doctor and will be used to plan your care.



Contact Information

Study Coordinator
Graham Keyes
[email protected]

Disclaimer: The information on this website is for general informational purposes only and SHOULD NOT be relied upon as a substitute for sound professional medical advice, evaluation or care from your physician or other qualified health care provider.