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)
City of Hope, Duarte, California, United States
UC Davis Medical Center, Sacramento, California, United States
The University of Chicago Medical Center, Chicago, Illinois, United States
German CLL Study Group, Cologne, Germany
Mayo Clinic in Arizona, Scottsdale, Arizona, United States
Mayo Clinic in Rochester, Rochester, Minnesota, United States
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
UCSD Moores Cancer Center, La Jolla, California, United States
Memorial Sloan Kettering Basking Ridge, Basking Ridge, New Jersey, United States
Memorial Sloan Kettering Monmouth, Middletown, New Jersey, United States
Memorial Sloan Kettering Bergen, Montvale, New Jersey, United States
Memorial Sloan Kettering Cancer Center, New York, New York, United States
Ohio State University, Columbus, Ohio, United States
Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Medical Center, Columbus, Ohio, United States
Huntsman Cancer Institute, Salt Lake City, Utah, United States
TG Therapeutics Investigational Trial Site, Ashkelon, Israel
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.