Bayer boosts hemophilia portfolio with European Jivi approval

28 November 2018

Leverkusen, Germany-based drugmaker Bayer (BAYN: DE) has been granted approval in Europe for Jivi (recombinant factor VIII concentrate).

The approval comes three months after the US regulator gave the hemophilia A therapy the nod, and two months after it was approved in Japan.

Jivi is the third hemophilia A treatment in Bayer's portfolio, after Kogenate (recombinant antihemophilic factor) and Kovaltry (recombinant antihemophilic factor), which had combined sales of 967 million euros ($1.13 billion) in 2017.

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