SCCA Lymphoma Clinical Trials
Brentuximab Vedotin for Non-Hodgkin Lymphoma (UW11026)
A phase 2 study of brentuximab vedotin in relapsed or refractory CD30-positive non-Hodgkin lymphoma (NHL)
| Status | Conditions | Phase | Study ID |
| Recruiting | Non-Hodgkin's Lymphoma | Phase II |
UW11026 NCT01421667 |
Summary
This is a single-arm, open-label, multicenter, phase 2 clinical trial to evaluate the efficacy and safety of brentuximab vedotin as a single agent in patients with CD30-positive non-Hodgkin lymphoma (NHL).
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Eligibility Criteria (must meet the following to participate in this study)
- Histologically-confirmed CD30-positive NHL
- Relapsed or refractory disease following at least 1 prior systemic therapy
- Measurable disease of at least 1.5 cm as documented by CT
- ECOG performance status less than or equal to 2
Exclusions (conditions that would prevent participation in this study)
- History of another primary invasive malignancy that has not been in remission for at least 3 years
- Current diagnosis of systemic or cutaneous anaplastic large cell lymphoma or mycosis fungoides
- B cell lymphoma previously treated with only single-agent rituximab or corticosteroids as monotherapy
- Known cerebral/meningeal disease
Last Updated
November 07, 2012See this trial at ClinicalTrials.gov
Access protocol and consent forms at Fred Hutchinson Cancer Research Center
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- Talk to your health care providers first before making decisions about your health care.
- Whether you are eligible for a research study depends on many things. There are specific requirements to be in research studies. These requirements are different for each study.
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