Chronic Lymphocytic Leukemia Clinical Trial

HuMax-CD20 in Chronic Lymphocytic Leukemia

Summary

The purpose of this trial is to determine the safety and efficacy of HuMax-CD20 as a treatment for Chronic Lymphocytic Leukemia.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Chronic Lymphocytic Leukemia
Circulating lymphocytes above a specific level
Circulating lymphocytes showing certain markers

Exclusion Criteria:

Previous treatment with rituximab or alemtuzumab within 6 months prior to enrollment in study.
Previous stem cell transplantation.
Received any of the following treatments within 4 weeks prior to entering this trial: A) Anti-cancer therapy, B) Glucocorticoids unless less than 10 mg per day, C) Radiotherapy.
HIV positivity.
Hepatitis B or hepatitis C.
Other cancerous diseases, except certain skin cancers and cervix cancer.
Certain serious medical conditions, including kidney or liver disease, some psychiatric illnesses, and stomach, heart, hormonal, nerve or blood diseases.
Participation in another trial with a different new drug 4 weeks prior to enrollment in study.
Current participation in any other clinical study.
Pregnant or breast-feeding women.
Women of childbearing age who are unable or unwilling to use adequate contraception.

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Study ID:

NCT00093314

Recruitment Status:

Withdrawn

Sponsor:

GlaxoSmithKline

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There is 1 Location for this study

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University of Iowa, Hospitals and Clinics
Iowa City Iowa, 52242, United States

How clear is this clinincal trial information?

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Study ID:

NCT00093314

Recruitment Status:

Withdrawn

Sponsor:


GlaxoSmithKline

How clear is this clinincal trial information?

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