Ballicules › Drugs › Ceritinib
Pronunciation: se-RI-ti-nib (zye-KAY-dee-a)
Mechanism of action: Ceritinib ballicule
What it is ALK tyrosine kinase inhibitor; ALK-positive lung cancer after crizotinib.
Why this one It overcomes several crizotinib resistance mutations.
What limits it Severe GI toxicity — diarrhea, nausea, vomiting — in most patients, reduced by taking it with food. Hepatotoxicity; CYP3A4-dependent.
Molecular structure: Ceritinib
FDA-approved for
ALK-positive non-small cell lung cancer (2014)
FDA label
Read the full label on DailyMed ↗
FDA dosing Population Start Target Max
ALK-positive metastatic NSCLC Adult 450 mg QD with food 450 mg QD with food
Renal Undefined
Hepatic Severe (Child-Pugh C): reduce dose ~1/3; no adjustment for mild/moderate
Instructions Take once daily with food If a dose is missed, make it up unless next dose is within 12 h If vomiting occurs, do not re-dose; continue next scheduled dose Dose reductions in 150 mg steps (450 -> 300 -> 150) for toxicity Unavoidable strong CYP3A inhibitor: reduce dose ~1/3
Available strengths
Cautions GI adverse reactions (diarrhea, nausea, vomiting) Hepatotoxicity (monitor LFTs at least monthly) Interstitial lung disease/pneumonitis QT interval prolongation Hyperglycemia Bradycardia Pancreatitis Embryo-fetal toxicity
Adverse reactions Diarrhea Nausea Abdominal pain Vomiting Fatigue
Pregnancy Can cause fetal harm (animal data and mechanism of action); avoid in pregnancy
Lactation No data; do not breastfeed during treatment and for 2 weeks after
Cost Ceritinib (ZYKADIA)
Strength #/mo generic $/mo CostPlus 150 mg tab 30 qd not offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Ceritinib is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.
Generic entry 2032 est.
Principal risk Severe GI toxicity; take with food
Classes and tags
Clinical profile
Therapeutic safety burden 3 / 4
Overdose danger 2 / 4
Weight-gain liability 0 / 4
Sedation liability 0 / 4
QT / Torsades 2 / 4
Direct muscarinic antagonism 0 / 4
Embryofetal risk 3 / 4
Legacy pregnancy category D
Defining liability Myelosuppression and agent-specific hepatic, cardiac, pulmonary, neurologic or reproductive toxicity require oncology monitoring.
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