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
- 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
Additional relevant MeSH terms: