Rayoqta (abicipar pegol)
- Region
- 🇪🇺 EU
- Active substance
- abicipar pegol
- Company
- Allergan Pharmaceuticals International Limited
- Status
- Application withdrawn
- Therapeutic area
- Macular Degeneration
- Application
- EMEA/H/C/005103
- ATC
- S01LA
- Official record
- www.ema.europa.eu
Indication
Abicipar Pegol Allergan is indicated in adults for the treatment of neovascular (wet) age-related macular degeneration (AMD).
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.