Chronic Lymphocytic Leukemia Clinical Trial

Phase I and II Study of Auranofin in Chronic Lymphocytic Leukemia (CLL)

Summary

The purpose of this study is to evaluate the safety and effectiveness of auranofin to treat patients with leukemia-cll/" >chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), or prolymphocytic lymphoma (PLL).

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

histologically confirmed B-cell chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), prolymphocytic leukemia arising from CLL/SLL or Richter's transformation according to WHO criteria who require therapy based on the 2008 revised IWCLL criteria.
Relapsed or refractory disease after receiving at least 1 prior therapy for CLL
At least 18 years old; ECOG status of 1 or less; life expectancy 2 months or greater
Adequate organ and marrow function (total bilirubin less than 1.5x IULN; ALT less than 2x IULN; serum creatinine less than 1.5x ULN)

Exclusion Criteria:

have had chemotherapy, radiotherapy or immunotherapy within 4 weeks prior to entering study
have not recovered from AEs due to agents administered more than 4 weeks prior
receiving any other investigational agent
known second malignancy that limits survival to less than 2 years
known HIV positive
uncontrolled intercurrent illness
pregnant or breastfeeding

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 2

Estimated Enrollment:

15

Study ID:

NCT01419691

Recruitment Status:

Completed

Sponsor:

University of Kansas Medical Center

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There is 1 Location for this study

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University of Kansas Cancer Center
Westwood Kansas, 66205, United States

How clear is this clinincal trial information?

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 2

Estimated Enrollment:

15

Study ID:

NCT01419691

Recruitment Status:

Completed

Sponsor:


University of Kansas Medical Center

How clear is this clinincal trial information?

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