Anti-CD19 CAR-T Cell Therapy for Patients With Refractory Systemic Lupus Erythematosus
研究概览
研究类型
注册 (估计的)
联系人和位置
学习地点
-
-
Minsk Oblast
-
Lyasny、Minsk Oblast、白俄罗斯、223040
- NN Alexandrov National Cancer Centre of Belarus
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
取样方法
研究人群
描述
Inclusion Criteria:
- A confirmed diagnosis of SLE according to the 2019 EULAR/ACR criteria.
- Subacute or acute SLE.
- SLE activity according to the SELENA-SLEDAI disease activity index screening score ≥6 and/or the requirement for prednisolone (or equivalent doses of methylprednisolone) at a dose greater than 7.5 mg/day (6 mg/day for methylprednisolone) to maintain lower disease activity.
- A history of two or more prior therapies (one of the drugs mycophenolate mofetil or cyclophosphamide, or the development of side effects/intolerance to these drugs).
- Patients aged 18 years or older.
- A medical consultation on the need for this treatment method using cell therapy.
- Written informed consent from the patient for treatment.
- Patient compliance with the treatment protocol.
- Adequate organ function.
Exclusion Criteria:
- Any change in therapy within 90 days prior to the planned administration of CAR-T cell therapy.
- Patient requiring renal replacement therapy.
- Active hepatitis B or active hepatitis C (HCV RNA positive).
- HIV-infected patients.
- Uncontrolled acute life-threatening bacterial, viral, or fungal infection (e.g., positive blood culture ≤ 72 hours before infusion).
- Unstable angina and/or myocardial infarction within 6 months prior to screening.
Previous or concomitant malignancy with the exception of:
- basal cell or squamous cell carcinoma (adequate wound healing is required before study entry);
- In situ carcinoma of the cervix or breast, without evidence of recurrence for at least 3 years prior to study entry;
- A primary malignant tumor that has been completely resected and in complete remission for ≥ 5 years.
- Pregnant and lactating women.
- Intolerance to the excipients of the cell product.
- Cardiac arrhythmia not controlled by medical therapy.
- Patients with active neurological autoimmune or inflammatory disorders (e.g., Guillain-Barré syndrome, amyotrophic lateral sclerosis).
- The presence of any primary immunodeficiency.
Socioeconomic or geographic circumstances that cannot guarantee adequate compliance with the protocol requirements for treatment and follow-up.
-
学习计划
研究是如何设计的?
设计细节
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 |
|---|---|---|
|
SELENA-SLEDAI activity index assessment and serologic remission (defined as normal level of primary (dsDNA and/or antiSm) and antiphospholipid antibodies (lupus anticoagulant (LA), AT to cardiolipinanti-dsDNA and normal complement C3 and C4 levels)
大体时间:36 months after CAR-T cells infusion
|
SELENA-SLEDAI (Safety of Estrogens in Lupus Erythematosus National Assessment - Systemic Lupus Erythematosus Disease Activity Index) Score Interpretation: 0 points: Remission / no activity 1-4 points: Low activity 5-10 points: Moderate activity > 10 points: High activity (Scores ≥ 6 typically indicate active disease requiring treatment) |
36 months after CAR-T cells infusion
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Evaluation of CAR T-Cell-Related Toxicities
大体时间:Start from 0 day up to 30 days after CAR-T cells infusion
|
Evaluation of Cytokine Release Syndrom (CRS) according NCCN guidelines version 2.2026. Immune Effector cell-associated Neurotoxicity Syndrom (ICANS) accordin NCCN guidelines version 2.2026. |
Start from 0 day up to 30 days after CAR-T cells infusion
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 20251677
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.