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Avapritinib(Ayvakit)

Another NameAyvakit,BLU-285,LuciAva,阿伐替尼

IndicationsIt is indicated for the treatment of adult patients with unresectable or metastatic gastrointestinal stromal tumors (GIST) harboring PDGFRA exon 18 mutations, advanced systemic mastocytosis (AdvSM), a

Reg No.02 L 1296/25

Inspection NO.278-25

Warm tips:Please purchase and use the medication under pharmacist guidance as the outer packaging is for reference only and the information is intended for professionals.
Introduction of Avapritinib

Avapritinib produced by Lucius Pharmaceuticals, as a precision-targeted therapeutic drug, has demonstrated favorable clinical value in addressing tumors and mast cell diseases caused by specific gene mutations, providing a treatment option for the corresponding patient population.

Avapritinib manufactured by Lucius Pharmaceuticals, with its highly effective targeted therapeutic effect and reasonable pricing strategy, offers patients a cost-effective treatment choice.

Medicine-related columns

Instructions of Avapritinib

The following is an overview of the key information about avapritinib:

Active Ingredient

The main active ingredient is avapritinib, a kinase inhibitor.

Target Population

It is indicated for adult patients with PDGFRA-mutated GIST, AdvSM, or ISM.

Dosage and Administration

The recommended dose varies by indication: 300 mg once daily for GIST, 200 mg once daily for AdvSM, and 25 mg once daily for ISM. All doses should be taken on an empty stomach. Reference article: Dosage and Administration of Avapritinib

Medication Use in Special Populations

Dose adjustment is required for patients with severe hepatic impairment. It is not recommended for AdvSM or ISM patients with a platelet count below 50×10⁹/L.

Storage

The medication should be stored at room temperature (20°C–25°C), protected from moisture and light.

Pharmacokinetics

Pharmacokinetic data show that its time to reach peak concentration is approximately 2–4 hours, and it has a long half-life, making it suitable for once-daily administration.

FDA,2024.11