A Study to Evaluate Corrected QT Interval From Clinical Studies Conducted With Bevacizumab

This study has been withdrawn prior to enrollment.
Information provided by:
Genentech, Inc.
ClinicalTrials.gov Identifier:
First received: May 21, 2007
Last updated: December 1, 2010
Last verified: December 2010
This is a supplemental study designed to evaluate the effect of bevacizumab on QTc interval in cancer patients. Patients who have consented to participate in selected randomized controlled bevacizumab clinical trials will be invited to participate in this study.

Condition Phase
Phase 4

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Evaluation of Corrected QT Interval From Clinical Studies Conducted With Bevacizumab

Further study details as provided by Genentech, Inc.:

Estimated Enrollment: 150
Study Start Date: June 2007

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Signed Informed Consent Form
  • Enrollment in one of a list of certain randomized, controlled bevacizumab trials

Exclusion Criteria:

  • Implantable pacemaker or automatic implantable cardioverter defibrillator (AICD)
  • Congenital long QT syndrome
  • Family history of long QT syndrome
  • Clinically significant bradycardia (defined as < 50 beats/minute)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00477425

Sponsors and Collaborators
Genentech, Inc.
Study Director: Jane Huang, M.D. Genentech, Inc.
  More Information

ClinicalTrials.gov Identifier: NCT00477425     History of Changes
Other Study ID Numbers: AVF4223g 
Study First Received: May 21, 2007
Last Updated: December 1, 2010
Health Authority: United States: Food and Drug Administration

Keywords provided by Genentech, Inc.:

ClinicalTrials.gov processed this record on May 24, 2016