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Hodgkin Lymphoma Molecular Profiling and Clinical Outcomes in U.S. Community Oncology Practices - CA209-655

Updated: 15 April, 2019   |

Print Friendly Summary

Print this page and the trial guide to help you talk with your doctor.
Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.

Trial Details

  • Gender(s)

  • 18+

    Age Range

  • 1


  • Recruiting

Treatment Options

Study Arms
Population with Condition

Key Eligibility Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit Inclusion Criteria: - Histologically confirmed diagnosis of Classical Hodgkin Lymphoma (cHL) - Patients who are treatment-naïve, or are within ± 2 weeks beginning any line of therapy at time of enrollment - Patients must be within ± 2 weeks of Day 1 of the first cycle of any line of therapy to enroll; a cycle is practice-defined for chemotherapy, targeted therapy, or immunotherapy-based regimens. - Any Eastern Cooperative Oncology Group (ECOG) or Karnofsky performance status (PS) - Patients must have available medical records for the date of diagnosis of cHL and available medical records documenting any prior treatment and treatment dates for the Hodgkin lymphoma, including chemotherapy, radiation, surgery and other anti-cancer therapy received. - Patients must consent for use of their FFPE tissue blocks for exploratory analyses Exclusion Criteria: - Patients on supportive care only and not receiving anti-cancer therapy are not eligible to enroll - Patients with unknown date of diagnosis of cHL - Patients whose prior cHL therapy, and dates of therapy (eg, surgery, radiation, or drug therapy) are unknown - Any other non-HL (non-Hodgkin Lymphoma) active malignancy for which the patient is receiving treatment - Patients participating in a clinical study that does not allow enrollment into a non-interventional study - Patients enrolled who go on to receive only supportive, palliative, hospice, or end-of-life care remain on study and should not be discontinued from follow-up. Other protocol defined inclusion/exclusion criteria could apply

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