VITRAKVI

This brand name is authorized in Austria, Brazil, Canada, Estonia, Finland, France, Hong Kong, Ireland, Israel, Japan, Lithuania, Netherlands, Poland, Turkey, United Kingdom, United States

Active ingredients

The drug VITRAKVI contains one active pharmaceutical ingredient (API):

1 Larotrectinib
UNII PF9462I9HX - LAROTRECTINIB

Larotrectinib is an adenosine triphosphate (ATP)-competitive and selective tropomyosin receptor kinase (TRK) inhibitor. The TRK family of proteins, TRKA, TRKB, and TRKC, is encoded by NTRK1, NTRK2 and NTRK3 genes. Larotrectinib was rationally designed to avoid activity with off-target kinases. It is indicated for the treatment of adult and paediatric patients with solid tumours that display a Neurotrophic Tyrosine Receptor Kinase (NTRK) gene fusion.

Read about Larotrectinib

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
VITRAKVI Hard capsule European Medicines Agency (EU) MPI, EU: SmPC
VITRAKVI Oral solution European Medicines Agency (EU) MPI, EU: SmPC
VITRAKVI Capsule / Oral solution FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
L01EX12 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01EX Other protein kinase inhibitors
Discover more medicines within L01EX12

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 538920030030007, 538920030030107, 538920040030407
Country: CA Health Products and Food Branch Identifier(s): 02490315, 02490323, 02490331
Country: EE Ravimiamet Identifier(s): 1801145, 1801156, 1801167
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 167776, 429452, 499084
Country: FR Base de données publique des médicaments Identifier(s): 64373909, 65942815, 67022406
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 377474, 392356, 392359
Country: HK Department of Health Drug Office Identifier(s): 66491, 66492, 66493
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8549, 8737
Country: JP 医薬品医療機器総合機構 Identifier(s): 4291071M1029, 4291071M2025, 4291071S1028
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1088495, 1088496, 1088497, 1092623
Country: NL Z-Index G-Standaard, PRK Identifier(s): 206156, 206164, 206172
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100426670, 100426718, 100426760
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699546156382, 8699546156399, 8699546650040
Country: US FDA, National Drug Code Identifier(s): 50419-390, 50419-391, 50419-392, 71777-390, 71777-391, 71777-392

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