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

This study has been withdrawn prior to enrollment.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00477425
First Posted: May 23, 2007
Last Update Posted: May 15, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Genentech, Inc.
  Purpose
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
Carcinoma

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

Resource links provided by NLM:


Further study details as provided by Genentech, Inc.:

Enrollment: 0
Actual Study Start Date: June 2007
Study Completion Date: June 2007
Primary Completion Date: June 2007 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00477425


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

ClinicalTrials.gov Identifier: NCT00477425     History of Changes
Other Study ID Numbers: AVF4223g
First Submitted: May 21, 2007
First Posted: May 23, 2007
Last Update Posted: May 15, 2017
Last Verified: May 2017

Keywords provided by Genentech, Inc.:
Avastin

Additional relevant MeSH terms:
Bevacizumab
Angiogenesis Inhibitors
Angiogenesis Modulating Agents
Growth Substances
Physiological Effects of Drugs
Growth Inhibitors
Antineoplastic Agents