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Update on CALAVI phase II trials for Calquence in patients hospitalised with respiratory symptoms of COVID-19.- AstraZeneca
The CALAVI Phase II trials for Calquence (acalabrutinib) in patients hospitalised with respiratory symptoms of COVID-19 did not meet the primary efficacy endpoint. The addition of Calquence to best supportive care (BSC) did not increase the proportion of patients who remained alive and free of respiratory failure. No new safety signal for Calquence was observed in the trials.
The CALAVI programme comprised two Phase II trials investigating acalabrutinib plus BSC versus BSC alone in hospitalised patients with COVID-19 disease. The safety and tolerability profiles for Calquence in the CALAVI Phase II trials were consistent with previous trials. The data will be presented in due course. Results from the CALAVI Phase II trials do not impact approved indications or pending approvals for Calquence in patients with blood cancers.
Condition: Coronavirus/COVID-19 Infection
Type: drug