Cenegermin
As of the edition of 20 October 2026, Cenegermin is a protein: marketed, first approved in 2017 (EU); acts on NTRK1, NTRK2 and NTRK3; US protection ends in 2030.
Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.
The drug
- Status
- Marketed; latest approval 2018
- Kind
- Protein
- Brand name
- Oxervate
- First approved
- 6 July 2017 (EU)
- Approvals on record
- 2 in 2 regions
- Holder of the most recent approval
- Dompé Farmaceutici; 2 holders in all
- Registered trials
- 24, 2 stopped early
- Disease areas
- Eye; Nervous system; Infections; Inherited and neonatal; Heart and blood vessels; Immune system
US protection
US protection ends in 2030.
US protection ends in 2030, 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 Dompé Farmaceutici. 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.
Companies that need a new molecule because of this drug
3 company-target rows on route B because of this drug.
Companies on route B for this drug
In the product3 company-target rows are on route B because of Cenegermin.
Targets
Registered trials
| Phase | Trials | Completed | Active | Stopped early |
|---|---|---|---|---|
| Phase not stated | 5 | 4 | 0 | 0 |
| Phase 1 | 5 | 3 | 0 | 1 |
| Phase 2 | 8 | 8 | 0 | 0 |
| Phase 3 | 4 | 2 | 2 | 0 |
| Phase 4 | 2 | 1 | 0 | 1 |
| All trials | 24 |
Who has held its approvals
| Company | Role | Years |
|---|---|---|
| Dompé Farmaceutici | Applicant and Lead sponsor of trials | 2012 to now |
| Dompe' Farmaceutici | Applicant | 2017 to now |