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Sam Chun Dang Pharm

Biosimilar developer, South Korea. 1 development product across 1 molecule: aflibercept.

First approval in the Atlas: Aug 2025, Eiyzey, aflibercept (EMA)
FDAproducts approved0
EMAproducts approved1
MHRAproducts approved1
PMDAproducts approved1
HCproducts approved0
CDSCOproducts approved0
EDEproducts registered0

Portfolio by market

MoleculeProductFDAEMAMHRAPMDAHCCDSCOEDEMarkets
AfliberceptEiyzey / Vgenfli SCD411·Aug 2025MHRASep 2025···3/7

Month shown is the first approval or registration of that product in that market.

In development

ClinicalTrials.gov lists one comparative trial sponsored by Sam Chun Dang Pharm for one molecule: aflibercept. All of these candidates already have at least one approval in the seven markets.

MoleculeCandidateDeveloper or sponsorReference productPhaseDesignRegistry statusStartedPrimary completionIn the AtlasRegistry record
AfliberceptSCD411Sam Chun Dang PharmEyleaPhase 3Comparative efficacyCompletedAug 2020Sep 2022Eiyzey / VgenfliNCT04480463

Registry data from ClinicalTrials.gov, entered by the sponsors and not verified by any regulator. Status and dates are as posted; sponsors often update them late. Trials registered only on other registries, such as India's CTRI or China's ChiCTR, are not included. Checked 12 Sep 2026.

Companies on the same molecules

Developers whose portfolios overlap most with Sam Chun Dang Pharm, by number of shared molecules. Overlap is the clearest sign of who competes with whom for the same tenders and licensing partners.

Chronology

Compare Sam Chun Dang Pharm with other developers on the comparison page.

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Data current to September 2026.