Personalized Reduction of Chemotherapy Intensity Through ctDNA Evaluation for the Treatment of Patients With Advanced Hodgkin Lymphoma

Abroad (travel likely)RecruitingPHASE2

Conditions

Advanced Hodgkin Lymphoma · Classic Hodgkin Lymphoma · Lugano Classification Stage III Hodgkin Lymphoma AJCC v8 · Lugano Classification Stage IV Hodgkin Lymphoma AJCC v8

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations
  • City of Hope, Irvine, California, United States

    Contact: Principal Investigator (Azra Borogovac, MD)
  • Stanford Cancer Institute Palo Alto, Palo Alto, California, United States

    Contact: Principal Investigator (Joseph Schroers-Martin, MD)
  • Dana-Farber Cancer Institute, Boston, Massachusetts, United States

    Contact: Principal Investigator (Reid Merryman, MD)
  • Washington University in St. Louis, St Louis, Missouri, United States

    Contact: Principal Investigator (David Russler-Germain, MD)
  • Memorial Sloan Kettering Cancer Center, New York, New York, United States

    Contact: Principal Investigator (Alison Moskowitz, MD)
  • Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington, United States

    Contact: Study coordinator (Hongyan Du, Ph.D.) · hongydu@fredhutch.org · 206-606-1221
    Contact: Principal Investigator (Ryan Lynch, MD)
Study leads
  • Ryan Lynch, MD

    Principal Investigator

    Fred Hutch/University of Washington Cancer Consortium