RYTELO

This brand name is authorized in United States.

Active ingredients

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

1
UNII F60NE4XB53 - IMETELSTAT
 

Imetelstat is an oligonucleotide telomerase inhibitor that binds to the template region of the RNA component of human telomerase (hTR), which prevents telomere binding. Telomerase activity and human telomerase reverse transcriptase (hTERT) RNA expression are known to be significantly increased in MDS and malignant stem and progenitor cells. Imetelstat treatment leads to reduction of telomere length, inhibition of malignant stem and progenitor cell proliferation and induction of apoptotic cell death leading to reduction of malignant clones.

 
Read more about Imetelstat

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 RYTELO Powder for concentrate for solution for infusion MPI, EU: SmPC European Medicines Agency (EU)
 RYTELO Solution for injection MPI, US: SPL/PLR FDA, National Drug Code (US)

Medicine classification

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

ATC Group Classification
L01XX80 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01X Other antineoplastic agents → L01XX Other antineoplastic agents
Discover more medicines within L01XX80

Authorization and marketing

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

Country Identification scheme Identifier(s)
US FDA, National Drug Code 82959-111, 82959-112

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