Elocta (efmoroctocog alfa)
- Region
- 🇪🇺 EU
- Active substance
- efmoroctocog alfa
- Company
- Swedish Orphan Biovitrum AB (publ)
- Status
- Authorised
- Therapeutic area
- Hemophilia A
- CHMP opinion
- Wed 23 Sep 2015
- EU approval
- Wed 18 Nov 2015
- Application
- EMEA/H/C/003964
- ATC
- B02BD02
- Official record
- www.ema.europa.eu
Indication
Treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency). Elocta can be used for all age groups.
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.