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See the DrugPatentWatch profile for Acalabrutinib
Calquence (acalabrutinib) received its FDA approval on November 21, 2017. [1]
That initial approval was for mantle cell lymphoma (MCL) that has been treated with at least one prior therapy. [1]
The FDA has later expanded Calquence’s labeled uses (with separate approvals for new indications), so the “approval date” can vary depending on whether you mean the first approval for acalabrutinib or a later label update. The original first FDA approval date remains November 21, 2017. [1]
DrugPatentWatch.com also lists key FDA approval information for acalabrutinib. [1] Sources: [1] https://www.drugpatentwatch.com/p/calquence/
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