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Biocon, Mylan get European Commission approval to market biosimilar insulin glargine


Biocon, Mylan get European Commission approval to market biosimilar insulin glargine

New Delhi: Biotechnology major Biocon and Mylan said their co-developed biosimilar insulin glargine has received marketing authorization approval from the European Commission (EC).

Semglee 100 units/mL 3 mL prefilled disposable pen for people with diabetes, is the first biosimilar from Biocon and Mylan’s joint portfolio to be approved in Europe, the companies said in a statement.

The Therapeutic Goods Administration (TGA) Australia has also approved the biosimilar product for people with diabetes in Australia, it added.

“We are excited to be able to bring Mylan and Biocon’s biosimilar insulin glargine to Europe and Australia where millions of people are currently living with diabetes…, Mylan President Rajiv Malik said.

The EC approval of Semglee applies to all 28 European Union (EU) member states and the European Economic Area (EEA) member states of Norway, Iceland and Liechtenstein, the statement said.

“The approval of Mylan and Biocon’s biosimilar insulin glargine by the European Commission and TGA Australia are important milestones in our collaboration,” Biocon CEO and Joint MD Arun Chandavarkar said.

In addition to these approvals, marketing applications for Semglee have also been submitted in Canada and the US. Several submissions are planned for key emerging markets, the statement said.

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Ruby Khatun

Ruby Khatun

Ruby Khatun joined Medical Dialogue as Reporter in 2016. She covers all the business news in different categories. She also covers all the updates in Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She is a post graduate from Jamia Hamdard. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751


Source: PTI
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