Acalabrutinib is an oral medicine. Current U.S. CALQUENCE capsule labeling recommends 100 mg approximately every 12 hours for the approved indications, although the exact regimen can require modification because of drug interactions or adverse reactions.

General administration

Patients prescribed acalabrutinib should:

The current U.S. capsule label specifically instructs patients to swallow capsules whole and states that CALQUENCE may be taken with or without food.

Missed dose

For current U.S. capsule labeling, if a dose is missed by more than three hours, the missed dose should be skipped and the next dose taken at its regularly scheduled time. Extra capsules should not be taken to replace the missed dose.

Drug interactions

Acalabrutinib exposure is affected by CYP3A-modifying medicines. Strong CYP3A inhibitors and strong CYP3A inducers should generally be avoided under U.S. labeling; certain moderate inhibitors require dosage modification.

Patients should tell their healthcare professional about prescription medicines, over-the-counter medicines, supplements and herbal products before treatment.

Monitoring

Treatment may require monitoring of:

The precise monitoring schedule depends on the patient’s condition and treatment regimen.

Storage

Storage requirements should be taken from the actual Acaluxen packaging and official product documentation. Acaluxen-specific storage instructions are Everest Pharmaceuticals Ltd.