Atorvastatin Combined With NAC Plus Romiplostim for Management of ITP
2026年6月19日 更新者:Fu Haixia、Peking University People's Hospital
Atorvastatin Combined With N-Acetyl-L-Cysteine Plus Romiplostim for Management of Steroid-Resistant/Relapsed Immune Thrombocytopenia
This is a prospective, single-arm, open-lable, single-center study and we aimed to determine whether atorvastatin combined with N-acetyl-L-cysteine (NAC) plus romiplostim could induce sustained response off-treatment (SRoT) in adult patients with ITP following CS failure.
研究概览
详细说明
This is a prospective, single-arm trial designed to investigate whether atorvastatin combined with N-acetyl-L-cysteine (NAC) plus romiplostim can induce a sustained response off-treatment (SRoT) in adult patients with immune thrombocytopenia (ITP) who experienced failure of first-line corticosteroid therapy.
In this study, SRoT is defined as an off-treatment period during which the platelet count remains above 30×10⁹/L in the absence of bleeding events or rescue therapy.
The primary endpoint was the proportion of patients who achieved SRoT by Week 24 after the discontinuation of romiplostim.
From Week 1 to Week 24, atorvastatin and NAC was administrated as the dose of 20mg qd and 400mg tid,respectively, and were discontinued at the end of Week 24.
During the initial 24 weeks, romiplostim was initiated at a starting dose of 3 μg/kg per week.
The weekly dose was adjusted based on platelet counts, with a maximum dose of 10 μg/kg per week, to maintain platelet levels within the range of 100-200×10⁹/L.
From Week 25 to Week 35, romiplostim was gradually tapered and discontinued, with the goal of maintaining a platelet count ≥30×10⁹/L and no less than twice the baseline level.
After all medications (including atorvastatin, NAC, and romiplostim) were discontinued (no later than Week 36), patients were followed up for an additional 24 weeks to evaluate the sustained response rate at 24 weeks post-treatment cessation.
研究类型
介入性
注册 (估计的)
50
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Fu Haixia, Dr.
- 电话号码:+861088326002
- 邮箱:fuhaixia_210@163.com
研究联系人备份
- 姓名:Xiaohui Zhang, Dr.
- 电话号码:861088326001
- 邮箱:zhangxh@bjmu.edu.cn
学习地点
-
-
-
Beijing、中国
- Peking University People's Hospital
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Diagnosed with primary ITP;
- Aged ≥18 years;
- Patients with treatment failure or relapse after first-line corticosteriod therapy for ITP;
- Platelet count <30×10⁹/L.
Exclusion Criteria:
- Pregnant or lactating women, and who were possibly pregnant, planning to become pregnant, or who had partners planning to become pregnant;
- Presence of active malignant tumors;
- Active HBV, HCV or HIV infection;
- Active infection requiring systematic treatment;
- Leukemia, myelodysplastic syndrome, aplastic anemia, myelofibrosis or other hematological disorders that may cause thrombocytopenia;
- History or presence of myocardial infarction, unstable ischemic heart disease, stroke, or NYHA Class IV heart failure;
- AST > 2 times the upper limit of normal (ULN), ALT > 2×ULN, or TBIL ≥ 1.5×ULN;
- eGFR < 50 mL/min/1.73m²;
- Any other subjects deemed ineligible for enrollment by the investigator.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:combined therapy
atorvastatin 20mg qd , N-acetyl-L-cysteine (NAC) 400mg tid, and romiplostim
|
From Week 1 to Week 24, atorvastatin and NAC was administrated as the dose of 20mg qd and 400mg tid,respectively, and were discontinued at the end of Week 24.
For romiplostim, the initial dose was 3 μg/kg per week.
The weekly dose was adjusted based on platelet counts, with a maximum dose of 10 μg/kg per week, to maintain platelet levels within the range of 100-200×10⁹/L during the initial 24-week period.
From Week 25 to Week 35, romiplostim was gradually tapered and discontinued with the goal of maintaining a platelet count ≥30×10⁹/L and no less than twice the baseline level.
After all medications (including atorvastatin, NAC, and romiplostim) were discontinued (no later than Week 36), patients were followed up for an additional 24 weeks to evaluate the sustained response rate at 24 weeks post-treatment cessation.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
24-week SRoT rate
大体时间:24 weeks post-treatment cessation
|
Sustained response off-treatment (SRoT) rate is defined as the proportion of patients who maintain a platelet count ≥30×10^9/L and at least a two-fold increase from the baseline count without active bleeding following treatment discontinuation.
|
24 weeks post-treatment cessation
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
24-week SCRoT rate
大体时间:24 weeks after treatment discontinuation
|
Sustained complete response off-treatment (SCRoT) rate was defined as the proportion of patients who maintain a platelet count of ≥100×10⁹/L without active bleeding after treatment discontinuation.
|
24 weeks after treatment discontinuation
|
|
ORR
大体时间:Up to the end of week 24
|
Overall response rate (ORR) is defined as the proportion of patients who achieve platelet count ≥30×10^9/L and more than twice the baseline level, with no signs of active bleeding.
|
Up to the end of week 24
|
|
CR rate
大体时间:Up to the end of week 24
|
Complete response (CR) rate is defined as the proportion of patients who achieve a platelet count ≥100×10⁹/L with no signs of active bleeding.
|
Up to the end of week 24
|
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TTR
大体时间:Up to the end of week 24
|
Time to response (TTR) is defined as the days from treatment initiation to first platete count reaching ≥30×10^9/L
|
Up to the end of week 24
|
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Sustained response
大体时间:Up to the end of week 24
|
Platelet count ≥30×10⁹/L and at least doubled from baseline on at least three of four scheduled visits during the final 8 weeks of the initial 24-week treatment phase without active bleeding.
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Up to the end of week 24
|
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Bleeding events
大体时间:Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
Bleeding incidence and severity per WHO bleeding score
|
Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
|
Adverse Events
大体时间:Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
The proportion of patients with adverse events
|
Up to the end of week 24; Week 25 to 24 weeks post-treatment cessation
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年6月1日
初级完成 (估计的)
2027年12月30日
研究完成 (估计的)
2028年12月30日
研究注册日期
首次提交
2026年5月16日
首先提交符合 QC 标准的
2026年6月19日
首次发布 (实际的)
2026年6月23日
研究记录更新
最后更新发布 (实际的)
2026年6月23日
上次提交的符合 QC 标准的更新
2026年6月19日
最后验证
2026年6月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 2025PHD049-001
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
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研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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