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CuraTeQ Biologics

Biosimilar developer, India. 4 development products across 4 molecules: bevacizumab, filgrastim, pegfilgrastim, trastuzumab.

First approval in the Atlas: Mar 2024, CuraTeQ Biologics Private (INN only), trastuzumab (CDSCO)
FDAproducts approved0
EMAproducts approved3
MHRAproducts approved3
PMDAproducts approved0
HCproducts approved0
CDSCOproducts approved2
EDEproducts registered0

About CuraTeQ Biologics

CuraTeQ is the biologics arm of Aurobindo. It received its first European approval, for filgrastim, in February 2025, and followed within months with pegfilgrastim and trastuzumab, with a second pegfilgrastim name given a positive opinion in 2026. In India it holds permissions for trastuzumab and bevacizumab. It is the newest Indian company to reach Europe.

Portfolio by market

MoleculeProductFDAEMAMHRAPMDAHCCDSCOEDEMarkets
BevacizumabCuraTeQ bevacizumab·····May 2026·1/7
FilgrastimZefylti·Feb 2025MHRA····2/7
PegfilgrastimDyrupeg / Cavoley·Mar 2025MHRA····2/7
TrastuzumabDazublys / CuraTeQ trastuzumab·Jun 2025MHRA··Mar 2024·3/7

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

Companies on the same molecules

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

Chronology

Compare CuraTeQ Biologics with other developers on the comparison page.

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Data current to September 2026.