Alprolix (eftrenonacog alfa)
Orphan
- Region
- 🇪🇺 EU
- Active substance
- eftrenonacog alfa
- Company
- Swedish Orphan Biovitrum AB (publ)
- Status
- Authorised
- Therapeutic area
- Hemophilia B
- EU approval
- Thu 12 May 2016
- Designations
- Orphan
- Application
- EMEA/H/C/004142
- ATC
- B02BD04
- Official record
- www.ema.europa.eu
Indication
Treatment and prophylaxis of bleeding in patients with haemophilia B (congenital factor IX deficiency).
Regulatory milestones
No milestones recorded in the last year.
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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.