Chronic Lymphocytic Leukemia Clinical Trial

Study of Weekly Motexafin Gadolinium (MGd) for Patients With Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Summary

The primary purpose of this study is to evaluate the safety, toxicities, dosage and response rate for an investigational drug, motexafin gadolinium, administered to patients with leukemia-cll/" >chronic lymphocytic leukemia or small lymphocytic lymphoma. The secondary purpose of this study is to evaluate the clinical benefit rate, the time it takes for a patient's chronic lymphocytic leukemia or small lymphocytic lymphoma to worsen, the duration of response and the time during which patients survive without chronic lymphocytic leukemia or small lymphocytic lymphoma worsening. Additionally, the patient's response to motexafin gadolinium will be compared to the response of the patient's cells in a laboratory to motexafin gadolinium.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

≥ 18 years old

CLL as defined by the NCI 96 criteria (exception; patients may have bright surface immunoglobulin staining if negative for t[11;14] translocation or cyclin D1) or SLL as defined by WHO classification criteria and is refractory or relapsed as defined by one of the following:

Refractory disease: progressive disease while on therapy
Relapsed disease: progressive disease after at least one treatment course of therapy with disease response or stabilization
ECOG performance status score of 0, 1, or 2
Willing and able to provide written informed consent

Exclusion Criteria:

Laboratory values of:

Platelet count < 30,000/µL
AST or ALT > 2 x ULN (upper limit of normal)
Total bilirubin > 2 x ULN
Creatinine > 2 mg/dL
Chemotherapy, radiation therapy, immunotherapy, systemic corticosteroids (> 10 mg oral prednisone or equivalent), or systemic biologic anticancer therapy within 21 days before beginning study treatment
Major surgery or hospitalization for a serious illness within the last 3 months
Greater than three prior regimens (where a regimen is defined as a treatment for CLL/SLL given initially or after disease progression)
Prior malignancy requiring current or prior treatment within the past 5 years, except for cervical neoplasia in situ and non-melanomatous skin cancer
Uncontrolled hypertension

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Estimated Enrollment:

35

Study ID:

NCT00290004

Recruitment Status:

Completed

Sponsor:

Pharmacyclics LLC.

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There are 4 Locations for this study

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USC Norris Cancer Hospital
Los Angeles California, 90033, United States
Scripps Cancer Center
San Diego California, 92121, United States
Northwestern University
Chicago Illinois, 60611, United States
The Mayo Clinic
Rochester Minnesota, 55905, United States

How clear is this clinincal trial information?

Study is for people with:

Chronic Lymphocytic Leukemia

Phase:

Phase 1

Estimated Enrollment:

35

Study ID:

NCT00290004

Recruitment Status:

Completed

Sponsor:


Pharmacyclics LLC.

How clear is this clinincal trial information?

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