Shanghai Junshi Biosciences Co. Ltd. announced that its new drug application (NDA) for roconkibart injection, a recombinant humanized anti-IL-17A monoclonal antibody intended for the treatment of adult patients with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy, has been accepted by the National Medical Products Administration. This marks a significant step in the regulatory review process for the company's new pharmaceutical product.
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