The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: Cardiac Safety Study of Brentuximab Vedotin (SGN-35)
Official Title: An Intensive QT/QTc Study to Investigate the Effects of SGN-35 (Brentuximab Vedotin) on Cardiac Ventricular Repolarization in Patients With CD30-Positive Malignancies
Study ID: NCT01026233
Brief Summary: The purpose of this study is to evaluate cardiac safety of brentuximab vedotin (SGN-35) in patients with CD30-positive cancers. The study will assess electrical activity of the heart before and after brentuximab vedotin administration. Patients who have stable or improving disease may receive up to 1 year of brentuximab vedotin treatment.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Alabama at Birmingham, Birmingham, Alabama, United States
City of Hope National Medical Center, Duarte, California, United States
Stanford Cancer Center, Stanford, California, United States
University of Miami Hospital and Clinics, Miller School of Medicine, Miami, Florida, United States
Cardinal Bernardin Cancer Center / Loyola University Medical Center, Maywood, Illinois, United States
New York University Cancer Institute, New York, New York, United States
Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States
Baylor University Medical Center, Dallas, Texas, United States
University Hospital of Cologne, Koln, , Germany
Name: Naomi Hunder, MD
Affiliation: Seagen Inc.
Role: STUDY_DIRECTOR