Indication
Details coming soon
Details coming soon
| Clinical Information | Administration Information |
|---|---|
|
Indication: Mantle Cell Lymphoma Condition: Patients who have received greater than or equal to 1 prior therapy |
Dose: by mouth – 100 mg Frequency: every twelve hours Note: Continue until disease progression or unacceptable toxicity |
|
Indication: Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma Condition: Monotherapy |
Dose: by mouth – 100 mg Frequency: every twelve hours Note: Continue until disease progression or unacceptable toxicity |
| Clinical Information | Administration Information |
|---|---|
|
Age: Pediatric |
Dose: No approved dosage available Note: No approved pediatric dosage available |
| Clinical Information | Administration Information |
|---|---|
|
Condition: Renal impairment Mild-to-moderate (eGFR greater than 30 mL/min/1.73m²) |
Dose: Tablet – No clinically relevant pharmacokinetics difference observed Note: No dosage adjustment required |
|
Condition: Renal impairment Severe (eGFR less than 30 mL/min/1.73m²) or patients on dialysis |
Dose: Tablet – Acalabrutinib pharmacokinetics has not been evaluated Note: Evaluation not available for severe impairment or dialysis patients |
| Drug Name | Risk Factors |
|---|---|
|
CYP3A inhibitors
|
Expected to increase acalabrutinib systemic exposure
|
|
CYP3A inducers
|
Expected to decrease acalabrutinib systemic exposure
|
| Disease Name | Risk Factors |
|---|---|
|
No specific contraindications listed
|
Monitor for general drug reactions
|
Details coming soon
Clinical & regulatory information on this page is compiled from the following government sources:
DISCLAIMER: This drug information content is provided for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Patients should always consult their physician with any questions regarding a medical condition and to obtain medical advice and treatment.