Study of the Bruton's Tyrosine Kinase Inhibitor in Subjects With Relapsed or Relapsed and Refractory Multiple Myeloma
Study Identifier
PCYC-1111-CA
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete
Results Available
Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English
Study Details
Medical Condition
Study Drug
Phase
Phase 2
Sex
Female & Male
Age
18+ years
Protocol Summary
The primary objective of this study is to determine the efficacy of PCI-32765, both as a single agent and in combination with dexamethasone, in subjects with relapsed or relapsed and refractory Multiple Myeloma (MM)
Study Locations
Location
Status
Location
SITE-13
La Jolla, California, United States, 92093
Status
Not applicable
Location
SITE-5
Baltimore, Maryland, United States, 21287
Status
Not applicable
Location
SITE-4
Boston, Massachusetts, United States, 02215
Status
Not applicable
Location
SITE-8
Ann Arbor, Michigan, United States, 48109
Status
Not applicable
Location
SITE-2
St Louis, Missouri, United States, 63110
Status
Not applicable
Location
SITE-6
Hackensack, New Jersey, United States, 07601
Status
Not applicable
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