AstraZeneca (LSE: AZN) and its hematology subsidiary Acerta Pharma have presented new, long-term follow-up results for Calquence (acalabrutinib) at the annual meeting of the American Society of Hematology.
The new data from the Phase II ACE-LY-004 trial in relapsed or refractory MCL showed sustained and clinically-meaningful responses to Calquence with a median follow-up of 26 months.
Initial data from this trial served as the basis for the accelerated approval of Calquence by the US Food and Drug Administration in October 2017.
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