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An expert panel hosted by
Customizing first-line BTK inhibitors for CLL
with Gilles Salles, Paolo Ghia, and Francesc Bosch
Wednesday, October 23, 2024
18:30-19:30 BST
This independent educational activity is supported by Pharmacyclics LLC, an AbbVie Company and Janssen Biotech. All content is developed independently by the faculty. The funder is allowed no influence on the content of this activity.
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On 23 July, 2020, acalabrutinib received a positive opinion by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA), recommending the granting of marketing authorisation for the treatment of adult patients with chronic lymphocytic leukemia (CLL).1
Acalabrutinib, a next-generation selective inhibitor of Bruton’s tyrosine kinase (BTK), was approved in the US for the treatment of adult patients with CLL and for adult patients with mantle cell lymphoma (MCL) who have received at least one prior therapy.2
The positive opinion was based on the results from two randomised, multicenter, open-label, phase III clinical trials:2
The CHMP recommendation is for1,2
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