Six More Biosimilars Lined Up For Approval By EMA

Three Ustekinumab Biosimilars And Three Other mAbs Receive CHMP Endorsement

Six biosimilars have received positive opinions from the European Medicines Agency’s Committee for Medicinal Products for Human Use at its July meeting.

Six hands with thumbs up
Six biosimilars have just received CHMP positive opinions • Source: Shutterstock

A slew of new biosimilars are lining up for approval in Europe, after the European Medicines Agency’s Committee for Medicinal Products for Human Use handed out positive opinions for six biosimilars at its July meeting.

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Accord’s Denosumab Biosimilars Get Thumbs-Up From EMA

 
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Accord received positive opinions for its Prolia and Xgeva biosimilars at the latest meeting of the EMA’s CHMP. Meanwhile, Celltrion picked up a nod for another Stelara biosimilar, while Rechon Life Science withdrew an application for human insulin.

Celltrion Plans Multiple US Biosimilar Launches In An ‘Exciting And Momentous’ Year

 
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With Celltrion having just received approval for its US Actemra (tocilizumab) biosimilar and having just launched its ustekinumab rival to Stelara – and with the introduction of the Korean developer’s denosumab rivals to Prolia and Xgeva just around the corner – 2025 is set to be a busy year, Celltrion USA chief commercial officer Thomas Nusbickel tells Generics Bulletin.

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Dr Reddy’s Bags Rights To Two More Biosimilars In Deal With Bio-Thera

 
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India’s Dr Reddy’s and China’s Bio-Thera have struck a deal covering ustekinumab and golimumab biosimilars in multiple markets in south-east Asia.