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Siliq (brodalumab) approved by the US FDA for adult patients with moderate-to-severe plaque psoriasis |
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16 February 2017
AstraZeneca’s partner Valeant Pharmaceuticals today announced that the US Food and Drug Administration (FDA) has approved Siliq (brodalumab) injection for the treatment of adult patients with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy and have failed to respond or have lost response to other systemic therapies. |
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