A Prospective, One-arm and Open Clinical Study to Assess Safety and Efficacy of Anti-Human CD20 Monoclonal Antibody Obinutuzumab in the Treatment of Primary Immune Thrombocytopenia
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 110
- 试验地点
- 1
- 主要终点
- Evaluation of overall efficacy response after Obinutuzumab treatment within 12 weeks
研究概览
简要总结
To evaluate the safety and efficacy of Obinutuzumab in the treatment of immune thrombocytopenia in patients who have not responded adequately or relapsed after first-line treatment.
详细描述
Immune thrombocytopenia (ITP) is an organ-specific autoimmune disease, which is characterized by decreased platelet count and skin and mucosal bleeding. ITP is a kind of disease with increased platelet destruction and impaired platelet production caused by autoimmunity. Conventional treatment of adult ITP includes first-line glucocorticoid and immunoglobulin therapy, second line TPO and TPO receptor agonist, splenectomy and other immunosuppressive treatments (such as rituximab, vincristine, azathioprine, etc.). ITP is one of the most common hemorrhagic diseases. At present, the treatment response of ITP is not good, and a considerable number of patients need drug maintenance treatment, which seriously affects the quality of life of patients and increases the economic burden of patients. Therefore, there is still a lack of effective treatment for adult ITP, especially for recurrent and refractory ITP patients, which is one of the problems that have attracted more attention and need to be solved urgently.
Obinutuzumab is the first personalized type Ⅱ glycosylation engineered CD20 monoclonal antibody. Studies have shown that compared with rituximab, obinutuzumab may improve its efficacy in lymphoma by increasing DCD and ADCC effects and reducing drug resistance by reducing CDC effects. In view of this, Obinutuzumab may have the same effect in the treatment of ITP, and may be more effective in the treatment of ITP, but there is also a risk of poor efficacy. At present, there is a lack of data on the efficacy and safety of Obinutuzumab in the treatment of ITP in China.
Therefore, the investigators designed this clinical trial to evaluate the safety and efficacy of Obinutuzumab in the treatment of immune thrombocytopenia in patients who have not responded adequately or relapsed after first-line treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 18 and above, male or female
- •Conform to the diagnostic criteria of immune Thrombocytopenia (ITP)
- •Diagnosis of ITP ≥3 months, and with a platelet count of <30 X 109/L measured within 2 days prior to administration（Platelet counts were measured at least 2 times during screening (at least 1 week apart) with platelets<30 X 109/L）
- •Failure to achieve response or relapse after corticosteroid therapy
- •The previous emergency treatment of ITP (e.g. methylprednisolone, platelet transfusion, IVIG transfusion) must be completed at least 2 weeks before the first administration
- •Signed and dated written informed consent
- •With Liver and kidney function<1.5×upper limit of normal， such as ALT、AST，BUN，Cre，etc.
- •ECOG physical state score ≤ 2 points
- •Cardiac function of the New York Society of Cardiac Function ≤ 2
- •Patients receiving maintenance treatment (including corticosteroids (less than or equal to 0.5mg/kg prednisone), TPO receptor agonists, etc.) must have a stable dose at least 4 weeks before the first administration, and azathioprine, danazol, cyclosporin A, tacrolimus, sirolimus, etc. must be stopped at least 4 weeks before the first administration; The end of rituximab treatment was>3 months；More than 6 months after splenectomy.
排除标准
- •Subjects with primary disease of important organs (liver, kidney, heart, etc.), or with immune system diseases;
- •Secondary thrombocytopenia caused by various reasons, such as connective tissue disorders, bone marrow hematopoietic failure disease, myelodysplastic syndrome, malignancy, drugs, inherited thrombocytopenia, common variable immune deficiency, lymphoma, etc.;
- •Subjects infected with human immunodeficiency virus (HIV);
- •Uncontrollable or active infections during the screening period, including hepatitis B, hepatitis C, cytomegalovirus, EB virus, or positive syphilis antigen;
- •Subjects with extensive and severe bleeding, such as hemoptysis, upper gastrointestinal hemorrhage, intracranial hemorrhage;
- •Subjects with heart disease that requires treatment or hypertension that has been judged by researchers to be poorly controlled currently;
- •Subjects with any venous or arterial thrombosis, atherosclerosis, and other diseases;
- •Subjects with a history of malignant solid tumor or have received allogeneic stem cell transplantation or organ transplantation;
- •Subjects with mental disorders who are unable to sign normal informed consent and conduct trials and follow-up;
- •Subjects whose toxic symptoms caused by pre-trial treatment have not disappeared;
- •Subjects with other serious diseases that may limit their participation in this trial (diabetes; severe cardiac insufficiency; myocardial obstruction or unstable arrhythmia or unstable angina pectoris in the last 6 months; gastric ulcer; active autoimmune disease, etc.);
- •Subjects with septicemia or other irregular bleeding;
- •Female subjects who are nursing or pregnant/suspected pregnant (positive pregnancy tests for human chorionic gonadotropin in urine during screening).
- •Patients taking antiplatelet drugs at the same time;
研究组 & 干预措施
Intervention (Obinutuzumab)
110 enrolled subjects: one infusion
干预措施: Obinutuzumab Injection [Gazyva] (Drug)
结局指标
主要结局
Evaluation of overall efficacy response after Obinutuzumab treatment within 12 weeks
时间窗: 12 weeks
Overall response rate defined as proportion of subjects with a platelet count ≥ 30 × 10\^9/L and at least 2-fold from baseline at the meanwhile within 12 weeks after initial administration in absence of rescue therapy, and without having had dose increment of TPO-RA or corticosteroids during the study period
次要结局
- Evaluation of sustained response rate after Obinutuzumab treatment within 6 months(6 months)
- Reduction of concomitant drug after Obinutuzumab treatment within 12 weeks(12 weeks)
- Number of subjects with clinically significant bleeding as assessed using the world health organization (WHO) bleeding scale after Obinutuzumab treatment within 12 weeks(12 weeks)
- Emergency treatment after Obinutuzumab treatment within 12 weeks(12 weeks)
- Evaluation of overall efficacy response after Obinutuzumab treatment within 8 weeks(8 weeks)
- Evaluation of overall efficacy response after Obinutuzumab treatment within 6 months(6 months)
- Evaluation of overall efficacy response after Obinutuzumab treatment within 12 months(12 months)
- Time to onset response(12 months)
- One-year recurrence-free survival rate(12 months)
- Safety of Anti-CD20 antibody treatment(12 months)
- Evaluation of sustained response rate after Obinutuzumab treatment within 12 months(12 months)
- Duration of response(12 months)