This brand name is authorized in Austria, Estonia, Spain, France, Hong Kong, Croatia, Ireland, Israel, Italy, Japan, Lithuania, Poland, United States
The drug LUTATHERA contains one active pharmaceutical ingredient (API):
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Lutetium ¹⁷⁷Lu oxodotreotide
UNII AE221IM3BB - LUTETIUM OXODOTREOTIDE LU-177
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Lutetium (177Lu) oxodotreotide has a high affinity for subtype 2 somatostatin receptors (sst2). It binds to malignant cells which overexpress sst2 receptors. Lutetium-177 (177Lu) is a βemitting radionuclide with a maximum penetration range in tissue of 2.2 mm (mean penetration range of 0.67 mm), which is sufficient to kill targeted tumour cells with a limited effect on neighbouring normal cells. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| LUTATHERA Solution for infusion | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| V10XX04 | V Various → V10 Therapeutic radiopharmaceuticals → V10X Other therapeutic radiopharmaceuticals → V10XX Various therapeutic radiopharmaceuticals | |
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): 1617184 |
| Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 1171226001 |
| Country: FR | Base de données publique des médicaments | Identifier(s): 60823764 |
| Country: HK | Department of Health Drug Office | Identifier(s): 66645, 66646 |
| Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 8801 |
| Country: IT | Agenzia del Farmaco | Identifier(s): 045677010 |
| Country: JP | 医薬品医療機器総合機構 | Identifier(s): 4291458A1020 |
| Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1084163 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100396207 |
| Country: US | FDA, National Drug Code | Identifier(s): 69488-003 |
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