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Amgen’s Kyprolis approved for multiple myeloma by NICE
Amgen's multiple myeloma drug Kyprolis has been approved by the UK's National Institute for Health and Care Excellence (NICE).
The regulator has ratified the drug for routine prescription via the NHS after an independent NICE committee found that the therapy does not cause serious side effects such as chronic pain from damaged tissue to the same extent as current treatments.
It will be made available for patients with multiple myeloma whose cancer has come back after one round of therapy, provided that their previous treatment did not include the drug bortezomib.
NICE estimates that 2,200 patients a year with multiple myeloma will benefit from access to this tolerable new treatment through the NHS following this approval.
Tony Patrikios, executive medical director of Amgen in the UK and Ireland, said: "We know that time free of disease is precious and are committed to advancing care for people with this difficult-to-treat blood cancer."
This comes after the firm applied for US and European regulatory approval earlier this month to include additional overall survival data on the label for Kyprolis, in order to offer clearer guidance on its benefits.
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