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03 Jun 19 AbbVie’s US Humira Monopoly: Four Years and $60 Billion of Additional Sales Protection

Posted at 14:34h in Biosimilars

Introduction Approximately $60 billion in US Humira sales will remain uncontested over the next four years...

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04 Mar 19 Early Biosimilars Pave the Way for Recent Launches in Europe

Posted at 14:11h in Biosimilars

Introduction With over a decade of real world biosimilar experience in Europe and now more than...

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08 Jan 19 Perjeta (Pertuzumab): Current Landscape and Biosimilar Potential

Posted at 13:22h in Biosimilars

Introduction With the recent announcement that NeuClone is developing a biosimilar candidate of Perjeta (pertuzumab), this...

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12 Oct 18 On Your Marks: The Humira Biosimilar Race begins, but not in the U.S.

Posted at 08:56h in Biosimilars

Introduction Five biosimilar copies of the world’s highest selling drug, Humira (adalimumab), are about to launch...

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04 Oct 18 Key Themes Emerging from The FDA Biosimilar Public Hearing

Posted at 11:07h in Biosimilars

Introduction With 27 speakers and 78 follow-up electronic submissions, the Food and Drug Administration’s (FDA) recent...

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24 Sep 18 A Shift in Regulatory Thinking – Are Confirmatory Phase III Studies Redundant for Biosimilars?

Posted at 06:30h in Biosimilars

In recent years biosimilar regulatory requirements across the world have converged and a broadly accepted...

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17 Sep 18 Introducing the NeuClone Biosimilar Brief

Posted at 04:46h in Biosimilars

The NeuClone Biosimilar Brief is a biosimilar industry publication written by NeuClone exploring biosimilar related...

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