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CSL cracks the genetic code of haemophilia B treatment

Yolanda Redrup
Yolanda RedrupRich List co-editor

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At the launch of the world’s first gene therapy for haemophilia B in late 2022, there were tears.

Patients had waited decades for the therapy named Hemgenix – created by local biotech giant CSL and uniQure – which promised to give them more freedom than they had ever known.

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    Original URL: https://www.afr.com/companies/healthcare-and-fitness/csl-cracks-the-genetic-code-of-haemophilia-b-treatment-20230913-p5e4d5