ZOKINVY

This brand name is authorized in United States. It is also authorized in Austria, Croatia, Estonia, France, Ireland, Israel, Italy, Lithuania.

Active ingredients

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

1
UNII IOW153004F - LONAFARNIB
 

Lonafarnib is a disease modifying agent that prevents farnesylation, thereby reducing the accumulation of aberrant progerin and progerin-like proteins in the cell’s inner nuclear membrane. This results in maintaining cell integrity and normal function.

 
Read more about Lonafarnib

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ZOKINVY Hard capsule MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

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

ATC Group Classification
A16AX20 A Alimentary tract and metabolism → A16 Other alimentary tract and metabolism products → A16A Other alimentary tract and metabolism products → A16AX Various alimentary tract and metabolism products
Discover more medicines within A16AX20

Authorization and marketing

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

Country Identification scheme Identifier(s)
EE Ravimiamet 3046788, 3046799
FR Base de données publique des médicaments 61837140, 66601425
IL מִשְׂרַד הַבְּרִיאוּת 9043, 9044
IT Agenzia del Farmaco 050224017, 050224029
LT Valstybinė vaistų kontrolės tarnyba 1095122, 1095123
US FDA, National Drug Code 73079-050, 73079-075

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