Skojoy (aflibercept)
Biosimilar
- Region
- 🇪🇺 EU
- Active substance
- aflibercept
- Company
- Amgen Technology (Ireland) UC
- Status
- Application withdrawn
- Therapeutic area
- Wet Macular Degeneration; Macular Edema; Retinal Vein Occlusion; Choroidal Neovascularization
- CHMP opinion
- Thu 30 Jan 2025
- Designations
- Biosimilar
- Application
- EMEA/H/C/006551
- ATC
- S01LA05
- Official record
- www.ema.europa.eu
Indication
Treatment of age-related macular degeneration (AMD) and visual impairment.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Eydenzelt Authorised · Celltrion Healthcare Hungary Kft.
- 🇪🇺 Ahzantive Authorised · Formycon AG
- 🇪🇺 Baiama Authorised · Formycon AG
- 🇪🇺 Afqlir Authorised · Sandoz GmbH
- 🇪🇺 Opuviz Authorised · Samsung Bioepis NL B.V.
- 🇪🇺 Yesafili Authorised · Biosimilar Collaborations Ireland Limited
- 🇪🇺 Pavblu Authorised · Amgen Technology (Ireland) UC
- 🇪🇺 Afiveg Authorised · STADA Arzneimittel AG
- 🇪🇺 Mynzepli Authorised · Advanz Pharma Limited
- 🇪🇺 Eyluxvi Authorised · Biolitec pharma Limited Zweigniederlassung Jena
- 🇪🇺 Vgenfli Authorised · Zaklady FarmaFarmaceutyczne Polpharma S.Aceutyczne Polpharma S.A.
- 🇪🇺 Eiyzey Authorised · Zaklady FarmaFarmaceutyczne Polpharma S.Aceutyczne Polpharma S.A.
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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.