Acute Myeloid Leukemia Clinical Trial

Brentuximab Vedotin in Patients With CD30-positive Nonlymphomatous Malignancies

Summary

This is an open-label, multicenter, phase 2 clinical trial to evaluate the antitumor activity of brentuximab vedotin as a single agent in patients with CD30-positive nonlymphomatous malignancies.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically-confirmed by central review CD30-positive nonlymphomatous malignancy
Have failed, refused, or have been deemed ineligible for standard therapy
Measurable disease
Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1 or a Karnofsky or Lansky Performance Status score greater than or equal to 70

Exclusion Criteria:

Primary diagnosis of lymphoma or central nervous system (CNS) malignancy
History of another primary invasive malignancy that has not been definitively treated or in remission for at least 3 years
Evidence of active cerebral/meningeal disease

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 2

Estimated Enrollment:

84

Study ID:

NCT01461538

Recruitment Status:

Completed

Sponsor:

Seagen Inc.

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There are 28 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
Rocky Mountain Cancer Centers - Aurora
Aurora Colorado, 80012, United States
Mayo Clinic Cancer Center
Jacksonville Florida, 32224, United States
Ocala Oncology Center
Ocala Florida, 34471, United States
Indiana University Simon Cancer Center
Indianapolis Indiana, 46202, United States
Dana-Farber Cancer Institute
Boston Massachusetts, 02215, United States
Minnesota Oncology Hematology P.A.
Minneapolis Minnesota, 55404, United States
New York Oncology Hematology, P.C.
Albany New York, 12206, United States
University Hospitals Case Medical Center
Cleveland Ohio, 44106, United States
Willamette Valley Cancer and Research / USOR
Eugene Oregon, 97401, United States
Northwest Cancer Specialists, P.C.
Tulatin Oregon, 97062, United States
St. Francis Hospital
Greenville South Carolina, 29605, United States
Texas Oncology - Bedford
Bedford Texas, 76022, United States
Texas Oncology - Medical City Dallas
Dallas Texas, 75230, United States
Texas Oncology - Dallas Presbyterian
Dallas Texas, 75231, United States
Texas Oncology Denton South
Denton Texas, 76210, United States
Texas Oncology - Fort Worth 12th Avenue
Fort Worth Texas, 76104, United States
MD Anderson Cancer Center / University of Texas
Houston Texas, 77030, United States
MD Anderson Cancer Center Leukemia Group
Houston Texas, 77030, United States
Texas Oncology - Central Austin Cancer Center
Round Rock Texas, 78731, United States
Cancer Centers of South Texas - HOAST
San Antonio Texas, 78229, United States
Texas Oncology - Waco
Waco Texas, 76712, United States
Oncology and Hematology Assoc of SW VA DBA Blue Ridge Cancer Care
Blacksburg Virginia, 24060, United States
Virginia Cancer Specialists, PC
Fairfax Virginia, 22031, United States
Puget Sound Cancer Centers
Edmonds Washington, 98026, United States
Cancer Care Northwest
Spokane Valley Washington, 99216, United States
Yakima Valley Memorial Hospital / North Star Lodge
Yakima Washington, 98902, United States

How clear is this clinincal trial information?

Study is for people with:

Acute Myeloid Leukemia

Phase:

Phase 2

Estimated Enrollment:

84

Study ID:

NCT01461538

Recruitment Status:

Completed

Sponsor:


Seagen Inc.

How clear is this clinincal trial information?

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