EU approval for self-administered Crysvita
Crysvita is used to treat the rare genetic condition X-linked hypophosphataemia
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Tag: Crysvita
Kyowa Kirin’s Crysvita wins EU approval for expanded XLH population
New approval includes older adolescents and adults with rare disease
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CHMP backs expanding scope of Kyowa Kirin’s Crysvita
The decision could see older adolescents and adults access the treatment for X-linked hypophosphataemia (XLH)
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XLH patients to get routine access to first new therapy in 30 years
For the first time in more than 30 years children and young adults in England and Wales with the rare bone disorder XLH will have access to a new treatment option via the NHS.
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NICE u-turn approves funding for rare disease therapy Crysvita
The National Institute for Health and Care Excellence (NICE) has changed its position on NHS funding for Kyowa Kirin International’s Crysvita, now endorsing the drug’s use to treat X-linked hypophosphataemia (XLH) in children and young people with growing bones in England and Wales.
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Rare disease therapy Crysvita to be barred from NHS
Children and young people with X-linked hypophosphataemia (XLH) are unlikely to get routine access to Kyowa Kirin’s Crysvita on the NHS.
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FDA clears first therapy for inherited rickets
US regulators have approved the first drug to treat adults and children with x-linked hypophosphatemia (XLH), a rare, inherited form of rickets.
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EU clears rare musculoskeletal disorder drug
Doctors can now treat children living in the EU with the rare, chronic progressive musculoskeletal disorder X–Linked Hypophosphataemia with Kyowa Kirin/Ultragenyx’ Crysvita following its conditional approval in the region.
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Seven therapies backed for EU approval
Seven therapies have been put forward for approval in the European Union, bringing closer new options for a range of conditions including Crohn’s disease, diabetes and cancer.
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