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Risankizumab.rzaa: an interleukin monoclonal antibody antagonist binding to the p19 subunit of human IL-23 cytokine

机译:Risankizumab.rzaa:白细胞介素单克隆抗体拮抗剂与人IL-23细胞因子的p19亚基的结合

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摘要

Plaque psoriasis is the commonest form of psoriasis affecting about 85% of those patients with the condition. Risankizumab was developed as a high-affinity humanized monoclonal antibody specific for the p19 subunit of interleukin-23 (IL-23p19). Clinical trials demonstrated that risankizumab was very effective in patients with moderate to severe plaque psoriasis causing total clearing of the condition as evidenced by Psoriasis Scalp Severity Index (PSSI100) and static Physician's Global Assessment (sPGA) of 0 in more than 50% of patients after 52 weeks of treatment. Risankizumab has been approved by the Food and Drug Administration (FDA) for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy or phototherapy as a dose of 150 mg administered by subcutaneous injection at week 0, week 4 and every 12 weeks thereafter.
机译:斑块性牛皮癣是牛皮癣的最常见形式,影响其条件的约85%的患者。 Risankizumab被开发为对白细胞介素-33(IL-23P19)的P19亚基特异的高亲和力人源化单克隆抗体。 临床试验表明,Risankizumab在中度至重度斑块牛皮癣的患者中非常有效,导致牛皮癣头皮严重指数(PSSI100)和静态医师的全球评估(SPGA)在50%以上的患者中所证明的患者的总体状况 治疗52周。 Risankizumab已被食品和药物管理局(FDA)批准用于治疗中度至重度斑块的牛皮癣,其成年人是系统治疗或光疗的候选者,作为在第0周,第4周和每周一次通过皮下注射给药的剂量为150毫克的剂量 此后12周。

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