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Kyowa Kirin Announces EU Approval for the Self-administration of CRYSVITA® ▼ (burosumab) to Treat X-Linked Hypophosphataemia (XLH)

Kyowa Kirin Announces EU Approval for the Self-administration of CRYSVITA® ▼ (burosumab) to Treat X-Linked Hypophosphataemia (XLH)
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Positive CHMP opinion for self-administered Crysvita

Positive CHMP opinion for self-administered Crysvita 10th May 2021 The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended Kyowa Kirin’s Crysvita for a new self-administration option to treat the rare metabolic bone disease X-linked hypophosphataemia (XLH). XLH is a rare, genetic disease that causes bone, muscle and joint abnormalities. Although the condition is not life-threatening, it may reduce an individual’s quality of life with a life-long and progressive burden. Currently, Crysvita (burosumab) is administered by subcutaneous injection, and will still need to be initiated by an experienced physician if the new self-administration option is ultimately approved.

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