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A Multi-Center Open-Label Study of the Bruton's Tyrosine Kinase (BTK) Inhibitor, Ibrutinib, in Combination With MEDI4736, in Subjects With Relapsed or Refractory Lymphomas
The purpose of this study is to evaluate the efficacy, safety and tolerability of the combination treatment of ibrutinib and MEDI4736 in subjects with relapsed or refractory lymphomas.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Site-0397
Birmingham, Alabama, United States
Site-0047
Duarte, California, United States
Site-0038
Stanford, California, United States
Site-0388
Miami, Florida, United States
Site-0126
Chicago, Illinois, United States
Site-0020/0173
Boston, Massachusetts, United States
Site-0729
Ann Arbor, Michigan, United States
Site-0130
Detroit, Michigan, United States
Site-0343
Hackensack, New Jersey, United States
Site-0402
Philadelphia, Pennsylvania, United States
Start Date
May 1, 2015
Primary Completion Date
November 1, 2017
Completion Date
November 1, 2017
Last Updated
June 27, 2019
61
ACTUAL participants
Ibrutinib
DRUG
MEDI4736
DRUG
Lead Sponsor
Pharmacyclics LLC.
Collaborators
NCT06337318
NCT05139017
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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