Clinical and Pathologic Studies in Non-Hodgkin's Lymphoma Patients Receiving Antibody Treatment

Sponsor
Stanford University (Other)
Overall Status
Completed
CT.gov ID
NCT00398372
Collaborator
Amgen (Industry), National Institutes of Health (NIH) (NIH)
500
1
106
4.7

Study Details

Study Description

Brief Summary

To characterize the molecular and cell biology of the tumor cells in lymphoma. The mechanism of monoclonal antibody treatment by rituximab or epratuzumab will also be examined.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Official Title:
Le20: Clinical and Pathologic Studies in Non-Hodgkin's Lymphoma Patients Receiving Antibody Treatment
Study Start Date :
Nov 1, 2000
Actual Primary Completion Date :
Jun 1, 2007
Actual Study Completion Date :
Sep 1, 2009

Outcome Measures

Primary Outcome Measures

  1. To characterize the molecular and cell biology of the tumor cells in lymphoma. [6 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria:Non-Hodgkin's Lymphoma Patients Receiving Antibody Treatment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Stanford University School of Medicine Stanford California United States 94305

Sponsors and Collaborators

  • Stanford University
  • Amgen
  • National Institutes of Health (NIH)

Investigators

  • Principal Investigator: Wen-Kai Weng, Stanford University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00398372
Other Study ID Numbers:
  • LYMNHL0031
  • 200114861
  • 77550
  • CA09287
  • CA111827
  • LYMNHL0031
First Posted:
Nov 10, 2006
Last Update Posted:
Jun 2, 2011
Last Verified:
Jul 1, 2010

Study Results

No Results Posted as of Jun 2, 2011