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Iclusig

Iclusig Drug Interactions

ponatinib

Manufacturer:

Patheon

Distributor:

Zuellig

Marketer:

Otsuka (Philippines)
Full Prescribing Info
Drug Interactions
Substances that may increase ponatinib serum concentrations: CYP3A inhibitors: Ponatinib is metabolized by CYP3A4.
Co-administration of a single 15 mg oral dose of Ponatinib (Iclusig) in the presence of ketoconazole (400 mg daily), a strong CYP3A inhibitor, resulted in modest increases in ponatinib systemic exposure, with ponatinib AUC0-∞ and Cmax values that were 78% and 47% higher, respectively, than those seen when ponatinib was administered alone.
Caution should be exercised and a reduction of the starting dose of Ponatinib (Iclusig) to 30 mg should be considered with concurrent use of strong CYP3A inhibitors such as clarithromycin, indinavir, itraconazole, ketoconazole, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin, troleandomycin, voriconazole, and grapefruit juice.
Substances that may decrease ponatinib serum concentrations: CYP3A inducers: Co-administration of a single 45 mg dose of Ponatinib (Iclusig) in the presence of rifampin (600 mg daily), a strong CYP3A inducer, to 19 healthy volunteers, decreased the AUC0-∞ and Cmax of ponatinib by 62% and 42%, respectively, when compared to administration of ponatinib alone.
Co administration of strong CYP3A4 inducers such as carbamazepine, phenobarbital, phenytoin, rifabutin, rifampicin, and St. John's Wort with ponatinib should be avoided, and alternatives to the CYP3A4 inducer should be sought, unless the benefit outweighs the possible risk of ponatinib underexposure.
Substances that may have their serum concentrations altered by ponatinib: Transporter substrates: In vitro, ponatinib is an inhibitor of P-gp and BCRP. Therefore, ponatinib may have the potential to increase plasma concentrations of co-administered substrates of P-gp (e.g., digoxin, dabigatran, colchicine, pravastatin) or BCRP (e.g., methotrexate, rosuvastatin, sulfasalazine) and may increase their therapeutic effect and adverse reactions. Close clinical surveillance is recommended when ponatinib is administered with these medicinal products.
Paediatric population: Interaction studies have only been performed in adults.
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