This brand name is authorized in Austria, Estonia, Finland, France, Croatia, Ireland, Israel, Italy, Lithuania, Poland, Romania, Turkey, United Kingdom, United States
The drug TRODELVY contains one active pharmaceutical ingredient (API):
1
Sacituzumab govitecan
UNII M9BYU8XDQ6 - SACITUZUMAB GOVITECAN
|
Sacituzumab govitecan binds to Trop-2-expressing cancer cells and is internalised with the subsequent release of SN-38 from a hydrolysable linker. SN-38 interacts with topoisomerase I and prevents re-ligation of topoisomerase I-induced single strand breaks. The resulting DNA damage leads to apoptosis and cell death. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
TRODELVY Powder for solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC | |
TRODELVY Powder for solution for infusion | FDA, National Drug Code (US) | MPI, US: SPL/PLR |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
L01FX17 | L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01F Monoclonal antibodies and antibody drug conjugates → L01FX Other monoclonal antibodies | |
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): 1867800 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 159417 |
Country: FR | Base de données publique des médicaments | Identifier(s): 67719704 |
Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 9256 |
Country: IT | Agenzia del Farmaco | Identifier(s): 049780012 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1093692 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100460464 |
Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W68365001 |
Country: TR | İlaç ve Tıbbi Cihaz Kurumu | Identifier(s): 8698760790310 |
Country: US | FDA, National Drug Code | Identifier(s): 55135-132 |
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