Ibrutinib is a small molecule that acts as an irreversible potent inhibitor of Burton's tyrosine kinase. It is designated as a targeted covalent drug and presented as a promising activity in B-cell malignancies in clinical trials. Ibrutinib was developed by Pharmacyclics Inc and was first approved by the FDA in November 2013 for the treatment of mantle cell ...
Ibrutinib is indicated for the treatment of the following conditions.
Chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL)
Waldenström's macroglobulinemia
Chronic graft-versus-host disease (cGVHD)
Mantle cell lymphoma (MCL)
Marginal zone lymphoma (MZL)
Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States
M D Anderson Cancer Center, Houston, Texas, United States
M D Anderson Cancer Center, Houston, Texas, United States
Stanford University Hospitals and Clinics, Stanford, California, United States
Hackensack University Medical Center, Hackensack, New Jersey, United States
University Hospital of Salzburg St Johanns Spital, Salzburg, Austria
The West Clinic, Memphis, Tennessee, United States
Site-0343, Hackensack, New Jersey, United States
Site-0397, Birmingham, Alabama, United States
Site-0047, Duarte, California, United States
Kantonsspital Aarau, Aarau, Switzerland
European Institute of Oncology, Milano, Italy
Kantonsspital - St. Gallen, St. Gallen, Switzerland
Virginia Oncology Associates, Norfolk, Virginia, United States
West Clinic, Germantown, Tennessee, United States
Northwest Cancer Specialists, PC, Vancouver, Washington, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.