Low-dose baricitinib plus danazol in primary immune thrombocytopenia: a randomized, controlled phase 2 trial

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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Publication Details

Journal
Nature Communications
Published
2026-07-25
DOI
https://doi.org/10.1038/s41467-026-75344-7
Primary Topic
Platelet Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Low-dose baricitinib plus danazol in primary immune thrombocytopenia: a randomized, controlled phase 2 trial

Zhenling Li, Q Chen, Dai‐Hong Liu, Huixin Liu et al.
Nature Communications
Platelet Disorders and Treatments
article

Low-dose baricitinib plus danazol in primary immune thrombocytopenia: a randomized, controlled phase 2 trial

Zhenling Li, Q Chen, Dai‐Hong Liu, Huixin Liu, Xiao‐Jun Huang, Hui Liu, Yun He, Zhuo‐Yu An, Chen‐Cong Wang, Ying‐Jun Chang, Liping Dou, Hongmei Jing, G W Feng, Xiang Zhao, Xiaohui Zhang, Hai‐Xia Fu, Li Li, H J Zhou, Yu-Jun Dong, Yue Jin, Qiu‐Sha Huang, Yang Wang, L Yang, H Q Jiang, Yi Liu, Xiao-Lu Zhu, Yuan-Yuan Zhang, Jin Lu, Jin Wu, Zhi-Xue Li, Zhao Wang, Peng Zhao, Qian Jiang
article en

Abstract

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.

Nature Communications
Capital Medical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking University (CN), China-Japan Friendship Hospital (CN), Chinese PLA General Hospital (CN), National Clinical Research Center for Digestive Diseases (CN), Beijing Luhe Hospital Affiliated to Capital Medical University (CN), Beijing Hospital (CN), Peking University People's Hospital (CN), Peking University First Hospital (CN), Peking University Third Hospital (CN), Beijing Children’s Hospital (CN), Beijing Friendship Hospital (CN), Beijing Tsinghua Chang Gung Hospital (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 9%
Platelet Disorders and Treatments
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