Prediction of Response to Certolizumab Pegol Treatment by Functional MRI of the Brain. A Multi-center, Randomized Double-blind Controlled Study Prediction of Response to Certolizumab-Pegol in RA (PreCePRA)
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 156
- 试验地点
- 6
- 主要终点
- Reaching low disease activity
研究概览
简要总结
By using functional MRI the investigators have recently shown that TNFi elicit rapid changes in brain function linked to the perception of RA [5]. Functional MRI represents a method allowing detecting tiny changes in neuronal activity by measuring alterations of blood flow in the context of neuronal activation. TNFi rapidly reversed the widespread activation of brain centers involved in pain such as the thalamus and the somatosensoric cortex, as well as those involved in the control, of mood and emotions such as the limbic system. Moreover, as small phase I study with 10 patients with RA showed that high brain activity detected in the functional MRI predicts clinical response to Certolizumab Pegol after 1 month, suggesting the central nervous system activity may be used as a tool to predict response to TNFi [8]. The rationale of this study is to test whether response to TNFi can be predicted by using functional MRI.
详细描述
Randomized double-blinded controlled multi-centre, study over 12 weeks, followed by a 12 weeks single blinded multicenter trial in 156 patients with RA with inadequate response to DMARD therapy. The study is composed of 3 arms with a 1:1:1 randomization at baseline: High functional MRI/400mg Certolizumab Pegol on week 0,2 and 4 followed by Certolizumab Pegol 200mg every two weeks for a total of 24 weeks; low functional MRI/400mg Certolizumab Pegol on week 0,2 and 4 followed by Certolizumab Pegol 200mg every two weeks for a total of 24 weeks with the possibility of early escape at week 12.
Patients who did not respond sufficiently according to EULAR response criteria (DAS28 reduction ≥ 1.2) to Certolizumab-Pegol (Treatment Arm A and Arm B) after 12 weeks will be off-Study and treated according to local guidelines.
Patients in the Placebo group with an EULAR response ≥ 1.2 reaching remission (DAS28 ≤ 2.6) will also be off study and treated according to the local guidelines or will be followed while they are in clinical remission. Patients with an EULAR response (DAS28 reduction ≥ 1.2) but not fulfilling the clinical remission criteria (DAS28 ≤ 2.6) will receive Certolizumab Pegol in week 12,14 and 16 with Certolizumab Pegol 400mg s.c. followed by s.c.injection of 200mg Certolizumab Pegol every two weeks till week 24.
In the situation that in one group sufficient patients will be randomized, fMRI done at screening, needs to be analyzed first to ensure that no further patient will be randomized with the randomization to the closed group. A blinded person, not involved either in the analysation of the fMRI nor in the treatment of the patients or the clinical assessments, will be responsible for the randomization list. If the next number on the randomization list represent the number of the closed group, the patient is not eligible for the study and will be treated according to local guidelines.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
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
- •Understands and voluntarily signs an informed consent form
- •Male or female, aged ≥ 18 years at time of consent
- •Must be able to adhere to the study visit schedule and other protocol requirements
- •Must satisfy the 2010 ACR/EULAR classification criteria for rheumatoid arthritis plus a disease duration of at least 6 months.
- •Must have active RA with a DAS28 ≥3.2
- •Must be RF and/or ACPA positive
- •≥ 3 swollen and/or tender joints of the hands
- •At screening- visit patients should have been treated without alterations of therapy for at least three months with DMARDS (i.e. Methotrexate) with or without concomitant use of steroids).
- •Glucocorticoids treatment up to 10mg prednisolone per day will be allowed at study entry.
排除标准
- •Individuals not able to understand and follow study protocol and not able to voluntarily sign informed consent
- •Individuals not willing to follow study protocol and sign informed consent
- •Individuals with claustrophobia, tattoos containing metal, magnetic endoprostheses, surgery on bone in between a time interval < 3 months.
- •Patients treated before with any biological or small molecule or medication under investigation for the treatment of RA.
- •Patients with serious or chronic infections within the previous 3 months
- •Opportunistic infections within the 6 months before screening
- •Cancer within the 5 years before screening (with the exception of treated and cured squamous or basal cell carcinoma of the skin)
- •History of severe congestive heart failure
- •Current signs or symptoms of severe, progressive, or uncontrolled renal, hepatic, hematologic, gastrointestinal (a.e.diverticulitis), endocrine, pulmonary, cardiac, neurologic or cerebral disease
- •Transplanted organ (with the exception of corneal transplantation done more than 3 months before screening)
- •Evidence of active tuberculosis
研究组 & 干预措施
Certolizumab Pegol
干预措施: Certolizumab Pegol (Drug)
Certolizumab Pegol
干预措施: Placebo (Drug)
Placebo
干预措施: Certolizumab Pegol (Drug)
Placebo
干预措施: Placebo (Drug)
结局指标
主要结局
Reaching low disease activity
时间窗: 6 months
Proportion of patients who reach low disease activity according to the DAS28 (DAS28 \< 3.2) during the first 12 weeks of study participation according their screening CNS activity measured by functional MRI.
次要结局
- Quality of Life(6 months)
- SF36(6 months)
- Remission(6 months)
- MRI(6 months)
- Adverse events(6 months)
- Number of patients who discontinue Certolizumab-Pegol(6 months)
- Normal fMRI(6 months)
- Ultrasound score(6 months)
- Bold signal(6 months)