Biosimilar trastuzumab co-developed by Biocon receives approval in the EU

Biocon

19 December 2018 - Ogivri, a biosimilar Trastuzumab jointly developed by Biocon and Mylan, has been approved in the EU. 

The European Commission has granted Marketing Authorization for Ogivri to our partner Mylan.

The European Medicines Agency's CHMP previously issued a positive opinion recommending approval of Ogivri as a biosimilar to Roche's Herceptin (Trastuzumab) on 18 October 2018.

Ogivri is indicated for the treatment of patients with HER2 positive early breast cancer, metastatic breast cancer and metastatic gastric cancer. Under supervision of the relevant healthcare professional it can be prescribed as either monotherapy or in combination with other medicines dependent on the relevant diagnosis.

Read Biocon press release

Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , Europe , Biosimilar