CuraTeQ Biologics receives UK MHRA approval for Dazublys?

CuraTeQ Biologics s.r.o., a wholly owned step-down subsidiary of Aurobindo Pharma, has obtained marketing authorisation from UK's Medicines and Healthcare products Regulatory Agency (MHRA) for Dazublys?, its trastuzumab biosimilar version.

Earlier in July 2025, Dazublys? has received the marketing authorisation in the European Union from the European Commission (EC).

This is CuraTeQ's fourth biosimilar to be approved by MHRA after the approval of Bevqolva? in December 2024 and Zefylti? in May 2025 and Dyrupeg? in June 2025.

Dazublys?, Zefylti?, and Dyrupeg? are also approved in the European Union.

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