Safety of PCI-32765 in Chronic Lymphocytic Leukemia

Completed · Phase 1/Phase 2

Conditions studied: B-cell Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma

In brief

The purpose of this study is to establish the safety and efficacy of orally administered PCI-32765 in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma.

Key facts

Study ID

NCT01105247

Run by

Pharmacyclics LLC.

People needed

133

Starts

2010-05-01

Expected to finish

2013-02-01

Last updated by the study team

2014-03-31

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• FOR TREATMENT-NAIVE GROUP ONLY: Men and women ≥ 65 years of age with confirmed diagnosis of CLL/SLL, who require treatment per NCI or International Working Group guidelines 15-18
• FOR RELAPSED/REFRACTORY GROUP ONLY: Men and women ≥ 18 years of age with a confirmed diagnosis of relapsed/refractory CLL/SLL following previous therapy(ie, failed ≥ 2 previous treatments for CLL/SLL and at least 1 regimen had to have had a purine analog [eg, fludarabine] for subjects with CLL)
• FOR HIGH-RISK RELAPSED/ REFRACTORYGROUP ONLY: Men and women ≥ 18 years of age with a confirmed diagnosis of relapsed/refractory CLL/SLL with suboptimal response to chemoimmunotherapy, defined as progression of disease within 24 months of initiation of a regimen containing at least a nucleoside analogue or bendamustine in combination with a monoclonal antibody or failure to respond to such a regimen. (Note: a minimum of 2 cycles of chemoimmunotherapy required for eligibility)
• ECOG performance status of ≤ 2
• Willing and able to participate in all required evaluations and procedures in this study protocol including swallowing capsules without difficulty

You may not qualify if…

• Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer from which the subject has been disease free for at least 2 years or which will not limit survival to < 2 years
• Any immunotherapy, chemotherapy, radiotherapy, or experimental therapy within 4 weeks before first dose of study drug (corticosteroids for disease-related symptoms allowed but require 1-week washout before study drug administration)
• Central nervous system (CNS) involvement by lymphoma
• Major surgery within 4 weeks before first dose of study drug
• Concomitant use of medicines known to cause QT prolongation or torsades de pointes
• Significant screening electrocardiogram (ECG) abnormalities including left bundle branch block, 2nd degree AV block type II, 3rd degree block, bradycardia, and QTc > 470 msec
• Lactating or pregnant

Where it is running

• Stanford University School of Medicine — Stanford, California, United States
• New York Presbyterian Hosptial Cornell Med Center — New York, New York, United States
• The Ohio State University — Columbus, Ohio, United States
• Willamette Valley Cancer Institute and Research Center — Springfield, Oregon, United States
• Sarah Cannon — Nashville, Tennessee, United States
• MD Anderson Cancer Center — Houston, Texas, United States
• Texas Oncology - Tyler — Tyler, Texas, United States
• University of Vermont and Fletcher Allen Health Care — Burlington, Vermont, United States
• Northwest Cancer Specialists, P.C. — Vancouver, Washington, United States
• Yakima Valley Memorial — Yakima, Washington, United States

Full record on ClinicalTrials.gov

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