This brand name is authorized in Austria, Brazil, Estonia, Spain, France, Croatia, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, United Kingdom
The drug LUXTURNA contains one active pharmaceutical ingredient (API):
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1
Voretigene neparvovec
UNII 2SPI046IKD - VORETIGENE NEPARVOVEC
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Voretigene neparvovec results to transduction of retinal pigment epithelial cells with a cDNA encoding normal human RPE65 protein (gene augmentation therapy), providing the potential to restore the visual cycle in patients with vision loss due to inherited retinal dystrophy. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| LUXTURNA Concentrate and solvent for solution for injection | 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 |
|---|---|---|
| S01XA27 | S Sensory organs → S01 Ophthalmologicals → S01X Other ophthalmologicals → S01XA Other ophthalmologicals | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 526520120098907 |
| Country: EE | Ravimiamet | Identifier(s): 1783649 |
| Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 1181331001 |
| Country: FR | Base de données publique des médicaments | Identifier(s): 69302990 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 379821 |
| Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 8480 |
| Country: IT | Agenzia del Farmaco | Identifier(s): 047423013 |
| Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1086767 |
| Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 199362 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100416513 |
| Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W68641001 |
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