达那唑
免疫系统
医学
小学(天文学)
免疫学
相(物质)
内科学
临床研究阶段
临床试验
胃肠病学
抗体
药理学
随机对照试验
生物信息学
作者
Peng Zhao,Zhuo‐Yu An,Hai‐Xia Fu,Yang Wang,G W Feng,Huixin Liu,Dai‐Hong Liu,Yi Liu,H J Zhou,Hui Liu,Zhao Wang,Yu-Jun Dong,Hongmei Jing,Zhenling Li,Li Li,Liping Dou,Qiu‐Sha Huang,Jin Wu,L Yang,Yue Jin
标识
DOI:10.1038/s41467-026-75344-7
摘要
This multicenter, randomized, controlled study was conducted to explore the safety and efficacy of low-dose baricitinib plus danazol for ITP patients who had failed corticosteroids and at least one recommended subsequent treatment. Participants were randomly assigned to receive baricitinib plus danazol (n = 108) or danazol alone (n = 108) by a central, interactive web-based system. Patients and caregivers were not blinded to group assignment. Efficacy assessments were performed in the intention-to-treat population by investigators blinded to group assignment. The primary endpoint was 6-month durable response. Forty-nine (45.4%) patients in the combination arm and 22 (20.4%) patients in the monotherapy arm achieved 6-month durable response (P < 0.001). The safety analysis set included patients who received at least one dose of study medication (n = 108 in the combination arm and n = 105 in the monotherapy arm). Fifty-two (48.1%) patients receiving baricitinib plus danazol and 47 (44.7%) patients receiving danazol alone reported at least one adverse event. Each arm reported two patients who developed an adverse event causing study discontinuation and one patient who developed a grade 3 or more severe adverse event. Low-dose baricitinib plus danazol might be a novel option for difficult-to-treat ITP. Funding: National Key Research and Development Program of China (No. 2023YFC2507800), National Natural Science Foundation of China (No. 82230004, No. 82430006, No. 82400157), Capital Health Development and Research of Special (No. 2022-1-4082), and Beijing Natural Science Foundation (No. 7242154 and No. 7232188). ClinicalTrials.gov identifier: NCT05852847. Achieving sustained response remains a challenge for patients with difficult-to-treat immune thrombocytopenia (ITP). Here, the authors report that low-dose baricitinib plus danazol may be effective for patients with difficult-to-treat ITP with acceptable safety profiles.
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