
Alecnib150 mg
Everest Pharmaceuticals Ltd.
Alectinib is a targeted anticancer medicine (ALK tyrosine kinase inhibitor) approved for: Metastatic ALK-positive non-small cell lung cancer (NSCLC): Treatment of adult patients with anaplastic…
Alectinib is a targeted anticancer medicine (ALK tyrosine kinase inhibitor) approved for:
Alectinib also has demonstrated CNS-penetrant activity and is used, per guideline recommendations (e.g., NCCN), for patients with brain metastases from ALK-positive NSCLC. Alectinib must only be started after confirmation of ALK-positive status by a validated diagnostic test, and treatment should be initiated and supervised by a physician experienced in the use of anticancer therapies (oncologist).
| Indication | Recommended Dose |
|---|---|
| ALK-positive metastatic NSCLC | 600 mg orally twice daily (1200 mg/day) with food, until disease progression or unacceptable toxicity. |
| Adjuvant treatment after tumor resection (ALK-positive NSCLC) | 600 mg orally twice daily with food, for a total of 2 years or until disease recurrence or unacceptable toxicity, whichever occurs first. |
| Severe hepatic impairment (Child-Pugh C) | Reduce dose to 450 mg orally twice daily with food. |
Capsules should be swallowed whole and not opened or dissolved. If a dose is missed or vomiting occurs after a dose, the next dose should be taken at the regular scheduled time. See Precautions and Warnings and Use in Special Populations for dose modifications required for adverse reactions.
Common side effects (occurring in ≥20% of patients) associated with Alectinib include:
Less common but serious adverse effects include hepatotoxicity, interstitial lung disease/pneumonitis, bradycardia, severe myalgia with CPK elevation (rhabdomyolysis), hemolytic anemia, and gastrointestinal perforation. See Precautions and Warnings for details on monitoring for these serious effects.
Alectinib is contraindicated in patients with known hypersensitivity to Alectinib or to any component of the formulation.
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