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
  • Blood Cancer - Chronic Lymphocytic Leukemia (CLL)
  • Blood Cancer - Small Lymphocytic Lymphoma (SLL)
  • Study Drug
  • PCI-32765
  • 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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