Advanced non-small cell lung cancer with a BRAF V600E mutation

Active Ingredient: Encorafenib

Indication for Encorafenib

Population group: only adults (18 years old or older)
Therapeutic intent: Curative procedure

Encorafenib in combination with binimetinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a BRAF V600E mutation.

For this indication, competent medicine agencies globally authorize below treatments:

450 mg once daily

For:

Dosage regimens

Oral, 450 milligrams encorafenib, once daily.

Detailed description

The recommended dose of encorafenib is 450 mg once daily, when used in combination with binimetinib.

Duration of treatment

Treatment should continue until the patient no longer derives benefit or the development of unacceptable toxicity.

Missed doses

If a dose of encorafenib is missed, the patient should only take the missed dose if it is more than 12 hours until the next scheduled dose.

Vomiting

In case of vomiting after administration of encorafenib, the patient should not take an additional dose and should take the next scheduled dose.

Dosage considerations

They may be taken with or without food. The concomitant administration of encorafenib with grapefruit juice should be avoided.

Active ingredient

Encorafenib

Encorafenib is a potent and highly selective ATP-competitive small molecule RAF kinase inhibitor. Encorafenib suppresses the RAF/MEK/ERK pathway in tumour cells expressing several mutated forms of BRAF kinase (V600E, D and K). Specifically, encorafenib inhibits in vitro and in vivo BRAFV600E,DandK mutant melanoma cell growth.

Read more about Encorafenib

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