OMJJARA

This brand name is authorized in Austria, Estonia, France, Croatia, Ireland, Lithuania

Active ingredients

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

1 Momelotinib
UNII 6O01GMS00P - MOMELOTINIB

Momelotinib and its major human circulating metabolite (M21), are inhibitors of wild type Janus Kinase 1 and 2 (JAK1/JAK2) and mutant JAK2V617F, which contribute to signalling of a number of cytokines and growth factors that are important for haematopoiesis and immune function. Momelotinib inhibits cytokine-induced STAT3 phosphorylation in whole blood from patients with myelofibrosis and inhibits hepcidin. Additionally, momelotinib and M21 are direct inhibitors of ACVR1, which further down regulates liver hepcidin expression resulting in increased iron availability and red blood cell production.

Read about Momelotinib

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
OMJJARA Film-coated tablet European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
L01EJ04 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01E Protein kinase inhibitors → L01EJ Janus-associated kinase (JAK) inhibitors
Discover more medicines within L01EJ04

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 3066117, 3066128, 3066139
Country: FR Base de données publique des médicaments Identifier(s): 65429862, 67024001, 68004140
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1098740, 1098741, 1098742

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