US protection ending in 2030: Injuries
As of the edition of 20 October 2026, 9 drugs have US protection that ends in 2030 in injuries; 7 of them have at least one company on route B because of it.
Sources: FDA Orange Book and Purple Book, other approval registers.
9 drugs
| Drug | US protection | Status | Holder | Target | Route B rows |
|---|---|---|---|---|---|
| Aflibercept | Ends 2030 (orphan exclusivity) | Marketed | Regeneron | PGF, VEGFA | 4 |
| Birch triterpenes | Ends 2030 (exclusivity) | Marketed | Chiesi Farmaceutici | 0 | |
| Cemiplimab | Ends 2030 (computed from the first US licence) | Marketed | Regeneron | PDCD1 | 2 |
| Cenegermin | Ends 2030 (computed from the first US licence) | Marketed | Dompé Farmaceutici | NTRK1, NTRK2, NTRK3 | 3 |
| Erenumab | Ends 2030 (computed from the first US licence) | Marketed | Amgen | CALCRL | 1 |
| Fremanezumab | Ends 2030 (computed from the first US licence) | Marketed | Teva | CALCA, CALCB | 4 |
| Lanadelumab | Ends 2030 (computed from the first US licence) | Marketed | Takeda | KLKB1 | 1 |
| Omadacycline | Ends 2030 (patent) | Marketed | Transcept Pharmaceuticals | 0 | |
| Sildenafil | Ends 2030 (exclusivity) | Marketed | Viatris | PDE5A | 3 |
Listed by name. A route B row is one company at one target; for a drug with one target that is the number of companies. US protection is the US only, and it is not the date generics or biosimilars can enter.
Which companies are on route B in 2030 in injuries
In the product7 of these 9 drugs have at least one company on route B. Which companies, and their scores, are in the product.
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