Voretigene neparvovec
As of the edition of 20 October 2026, Voretigene neparvovec is a gene: marketed, first approved in 2017 (US); US protection ends in 2029.
Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.
The drug
- Status
- Marketed; latest approval 2020
- Kind
- Gene
- Brand name
- Luxturna
- First approved
- 19 December 2017 (US)
- Approvals on record
- 3 in 3 regions
- Holder of the most recent approval
- Novartis; 3 holders in all
- Registered trials
- 5, 0 stopped early
- Disease areas
- Eye; Inherited and neonatal
US protection
US protection ends in 2029.
US protection ends in 2029, computed as 12 years from the first US licence because FDA publishes no date for this product. The application that gives this date is held by Roche. The date is computed, not published.
This is the US only, and it is not the date generics or biosimilars can enter.
The exact date and the listings behind it
In the product2 listings count towards this date. The exact date and each listing are in the product.
See the exact date and the 2 listings behind itRequest access. Nothing is shown until you do.
Registered trials
| Phase | Trials | Completed | Active | Stopped early |
|---|---|---|---|---|
| Phase not stated | 2 | 1 | 1 | 0 |
| Phase 1 | 1 | 1 | 0 | 0 |
| Phase 2 | 1 | 0 | 1 | 0 |
| Phase 3 | 1 | 0 | 1 | 0 |
| All trials | 5 |