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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00142155
Other study ID # 02-075
Secondary ID
Status Completed
Phase N/A
First received September 1, 2005
Last updated June 23, 2011
Start date January 2002
Est. completion date March 2007

Study information

Verified date June 2011
Source Dana-Farber Cancer Institute
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if the type of Fc gamma RIIIa receptor that a particular patient's immune cells possess influences how they respond to rituximab and other monoclonal antibodies.


Description:

- A medical data collection survey sheet will be filled out by the patient or doctor with medical information pertaining to how the patient responded to rituximab and other monoclonal antibodies for use in this study.

- Blood work will be performed to analyze the blood by molecular technology to find the kind of Fc gamna RIIIa receptor the patient possess and correlate these findings with the outcome of treatment with rituximab or other monoclonal antibodies.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date March 2007
Est. primary completion date March 2007
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 90 Years
Eligibility Inclusion Criteria:

- Patients treated with rituximab or other monoclonal antibodies for Waldenstrom's macroglobulinemia

Study Design

N/A


Intervention

Drug:
Rituximab

monoclonal antibodies


Locations

Country Name City State
United States Dana-Farber Cancer Institute Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Dana-Farber Cancer Institute

Country where clinical trial is conducted

United States, 

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