Safety of PCI-32765 in Chronic Lymphocytic Leukemia
Study Identifier
PCYC-1102-CA
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Complete
Study Details
Medical Condition
Study Drug
Phase
Phase 1/Phase 2
Sex
Female & Male
Age
18+ years
Protocol Summary
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.
Study Locations
Location
Status
Location
Stanford University School of Medicine
Stanford, California, United States, 94305
Status
Not applicable
Location
New York Presbyterian Hosptial Cornell Med Center
New York, New York, United States, 10065
Status
Not applicable
Location
The Ohio State University
Columbus, Ohio, United States, 43210
Status
Not applicable
Location
Willamette Valley Cancer Institute and Research Center
Springfield, Oregon, United States, 97477
Status
Not applicable
Location
Sarah Cannon
Nashville, Tennessee, United States, 37203
Status
Not applicable
Location
MD Anderson Cancer Center
Houston, Texas, United States, 77030
Status
Not applicable
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