EirGenix

Biosimilar developer, Taiwan. 1 development product across 1 molecule: trastuzumab.

First approval in the Atlas: Nov 2023, Herwenda, trastuzumab (EMA)
FDAproducts approved0
EMAproducts approved1
MHRAproducts approved0
PMDAproducts approved0
HCproducts approved0
CDSCOproducts approved0
EDEproducts registered0

Portfolio by market

MoleculeProductFDAEMAMHRAPMDAHCCDSCOEDEMarkets
TrastuzumabHerwenda EG12014·Nov 2023·····1/7

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

In development

ClinicalTrials.gov lists one comparative trial sponsored by EirGenix for one molecule: pertuzumab. Candidates without an approval yet in the seven markets: EG1206A.

MoleculeCandidateDeveloper or sponsorReference productPhaseDesignRegistry statusStartedPrimary completionIn the AtlasRegistry record
PertuzumabEG1206AEirGenixPerjetaPhase 1Comparative PKCompletedMay 2022Jan 2023no approval in the seven marketsNCT05471648

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 EirGenix, by number of shared molecules. Overlap is the clearest sign of who competes with whom for the same tenders and licensing partners.

Chronology

Compare EirGenix with other developers on the comparison page.

Considering a partner, a licence or a new market for a biosimilar portfolio? EvySaif's regulatory strategy and value dossier work covers the regulatory and market-access side of that decision.

Planning your biosimilar strategy?

EvySaif can help assess your regulatory pathway, clinical evidence requirements and market-entry strategy across India, UAE and other target markets.

Talk to a biosimilar regulatory consultant
Data current to September 2026.