Non Hodgkin Lymphoma Clinical Trial

A Study of Brentuximab Vedotin in Relapsed or Refractory Non-Hodgkin Lymphoma

Summary

This is an 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) (Part A). The study will also evaluate the safety and efficacy of brentuximab vedotin in combination with rituximab in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) (Part B) as well as further evaluate correlation of CD30 expression and response in DLBCL (Part C).

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically-confirmed NHL (DLBCL only for Parts B and C)
Relapsed or refractory disease following at least 1 prior systemic therapy
Measurable disease of at least 1.5 cm as documented by CT
Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 2

Exclusion Criteria:

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 (for patients receiving brentuximab vedotin only) or corticosteroids as monotherapy
Known cerebral/meningeal disease

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

176

Study ID:

NCT01421667

Recruitment Status:

Completed

Sponsor:

Seagen Inc.

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There are 34 Locations for this study

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University of Alabama at Birmingham
Birmingham Alabama, 35294, United States
City of Hope
Duarte California, 91010, United States
PMK Medical Group Inc., DBA Ventura County Hematology Oncology Specialists
Oxnard California, 93030, United States
Stanford Cancer Center
Stanford California, 94305, United States
Rocky Mountain Cancer Centers - Aurora
Aurora Colorado, 80012, United States
Colorado Blood Cancer Institute
Denver Colorado, 80218, United States
Cancer Specialists of North Florida - St. Augustine
St. Augustine Florida, 32086, United States
Emory Winship Cancer Institute
Atlanta Georgia, 30322, United States
Northwestern University
Chicago Illinois, 60611, United States
University of Chicago
Chicago Illinois, 60637, United States
Dana-Farber Cancer Institute
Boston Massachusetts, 02215, United States
Minnesota Oncology Hematology P.A.
Minneapolis Minnesota, 55404, United States
Washington University School of Medicine
St. Louis Missouri, 63110, United States
Comprehensive Cancer Centers of Nevada
Las Vegas Nevada, 89169, United States
Hackensack University Medical Center
Hackensack New Jersey, 07601, United States
New York Oncology Hematology, P.C.
Albany New York, 12206, United States
NYU Clinical Cancer Center
New York New York, 10016, United States
Columbia University Medical Center
New York New York, 10019, United States
Memorial Sloan Kettering Cancer Center
New York New York, 10021, United States
Cleveland Clinic, The
Cleveland Ohio, 44195, United States
Willamette Valley Cancer and Research / USOR
Eugene Oregon, 97401, United States
Medical University of South Carolina
Charleston South Carolina, 29425, United States
St. Francis Hospital
Greenville South Carolina, 29605, United States
Texas Oncology - Medical City Dallas
Dallas Texas, 75230, United States
Charles A. Sammons Cancer Center
Dallas Texas, 75246, United States
Texas Oncology-Southwest Fort Worth
Fort Worth Texas, 76132, United States
MD Anderson Cancer Center / University of Texas
Houston Texas, 77030, United States
Texas Oncology - Seton Williamson
Round Rock Texas, 78665, United States
Texas Oncology - Tyler
Tyler Texas, 75702, United States
Virginia Cancer Specialists, PC
Fairfax Virginia, 22031, United States
Swedish Cancer Institute Medical Oncology
Edmonds Washington, 98026, United States
Seattle Cancer Care Alliance / University of Washington Medical Center
Seattle Washington, 98109, United States
Northwest Cancer Specialists, P.C.
Vancouver Washington, 98684, United States
British Columbia Cancer Agency - Vancouver Centre
Vancouver British Columbia, V5Z 4, Canada

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

176

Study ID:

NCT01421667

Recruitment Status:

Completed

Sponsor:


Seagen Inc.

How clear is this clinincal trial information?

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