Assessment of Structural Benefits of Injectable Abatacept as Measured by MRI in RA Patients Who Have Failed Prior Anti-Tumor Necrosis (TNF) Therapy and Correlated With Clinical Outcomes
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 34
- 试验地点
- 1
- 主要终点
- Number of Participants With an Improvement in Bone Edema/Osteitis on Low-field MRI in Rheumatoid Arthritis Patients on Weekly SC Abatacept in Combination With Methotrexate Over a 12-month Period.
研究概览
简要总结
The purpose of this study is to determine if the use of sub-cutaneous (SC) abatacept provides any structural benefit in patients with rheumatoid arthritis who have failed prior use of TNF therapy.
详细描述
Results in the literature suggest the structural benefits of intravenous (IV) abatacept as measured by high and low field MRI and X-ray in patients with rheumatoid arthritis who have previously failed clinical treatment with TNF agents. This study attempts to measure the structural benefits of SC abatacept in a similar cohort of patients while at the same time comparing the structural findings with clinical outcome measurements as collected at corresponding time points with an automated patient and physician disease activity scoring system of 28 joints (DAS28).
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
- 是
入选标准
- •Able and willing to give written informed consent
- •Patients must have a diagnosis of rheumatoid arthritis > 3 months
- •Patients must have been receiving methotrexate for 12 weeks prior to screening at a dose of 10mg - 25 mg weekly.
- •Patient must have had an inadequate response after receiving or previously receiving one (1) but no more than two (2) anti-TNF biologic agents
- •Age >/= 18 yrs
- •Must have active RA as defined by a DAS28 (Erythrocyte sedimentation rate) score >4.4
- •Must have synovitis of at least two joints in one hand/wrist at screening and baseline
- •Must have a negative Pregnancy test and use adequate method of contraception throughout the trial
- •Stable use of Corticosteroids is permitted
- •Stable use of Non-steroidal anti-inflammatory drugs is permitted
排除标准
- •Functional Class IV
- •Pregnancy or breastfeeding
- •History of any other inflammatory arthritis
- •Sexually active patients who are not using acceptable birth control
- •Subjects who have undergone metacarpophalangeal (MCP) arthroplasty or anticipate the need for such a procedure
- •Subjects with a history of cancer in the last five years other than non melanoma skin cancers
- •Subjects who are unable to comply with study and followup procedures
- •Subjects who have current or severe symptoms of renal, hepatic, hematologic, gastrointestinal, pulmonary cardiac, neurologic, or cerebral disease
- •Subjects who currently abuse drugs or alcohol
- •Subjects with evidence of active or latent bacterial or viral infections at the time of enrollment
- •Subjects who have received live vaccines within 4 months of first dose of study medication
- •Subjects with herpes zoster or cytomegalovirus that resolved less than two months prior to dosing
- •Subjects at risk for tuberculosis (TB). Specifically excluded will be subjects with a history of active TB within the last 3 years and subjects with latent TB must have a negative chest X-ray and be started on treatment for at least 28 days prior to dosing.
- •Prior treatment with Rituximab within 12 months
- •Prior treatment with more than 2 TNFs
- •Intramuscular(IM), Intravenous(IV) Intra-articular (IA) corticosteroids within 28 days prior to baseline
- •Subjects who have a metal device affected by MRI (e.g. any type of electronic, mechanical or magnetic implant, metal slivers, metal objects, cardioverter defibrillator)
- •Subjects who have received any disease modifying agent (DMARD) other than methotrexate within the past 28 days prior to baseline
研究组 & 干预措施
abatacept
open label use of abatacept for 12 months
干预措施: abatacept (Biological)
结局指标
主要结局
Number of Participants With an Improvement in Bone Edema/Osteitis on Low-field MRI in Rheumatoid Arthritis Patients on Weekly SC Abatacept in Combination With Methotrexate Over a 12-month Period.
时间窗: MRIs at Baseline and Week 48
bone edema/osteitis using low-field MRI analysis of 25 anatomical locations in the wrist and hand and scoring the volume of the original articular bone in 0.5 increments from 0-3, with each increment in the scale representing 33% of the volume of the peripheral 1 cm of original (eroded + residual) articular bone.
次要结局
- Number of Patients With Adverse Events(all adverse events will be captured from Day 1 up to 52 weeks)
- Patients With an Improvement in DAS Score Were Considered Responders at Week 48(The DAS 28 score will be performed at baseline and 48)
- To Measure the Change From Baseline in Patient DAS 28 Scores at Baseline and Weeks 12, 24(Patient DAS 28 scores will be measured at baseline and weeks 12, 24, 48 and disease activity will be recorded at Week 48)
- the Clinical Outcomes Measurements (American College of Rheumatology Activity Scoring, Health Assessment The Number of Patients With a Clinical Response at Week 24 and 48(week 24 and Week 48)
研究者
Norman B. Gaylis, MD
MD
Arthritis & Rheumatic Disease Specialties Research