VELVET (Veltuzumab Various Doses Exploratory Trial), a Randomized, Double Blind, Placebo Controlled, Multicentre, Multinational Phase II Dose Range Finding Trial in Subjects With Moderate to Severe Rheumatoid Arthritis Insufficiently Controlled With Either Methotrexate Alone or Methotrexate Plus Anti-tumour Necrosis Factor Biological Treatment, Comparing 3 Different Subcutaneous Dosages of Anti-CD20 Monoclonal Antibody Veltuzumab to Placebo as an add-on Therapy to Methotrexate.
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 发起方
- 入组人数
- 300
- 试验地点
- 1
- 主要终点
- American College of Rheumatology 20 (ACR20) response rate at completion of week 24
研究概览
简要总结
This is a multi-national, multi-centre, placebo-controlled, double-blind, randomized, 4-arm parallel group trial, comparing three different dose levels (80 mg, 160 mg and 320 mg) of veltuzumab to placebo, administered weekly (days 1, 8, 15 and 22) by subcutaneous (sc) injection to subjects with moderate to severe rheumatoid arthritis (RA) (cumulative veltuzumab doses 320 mg, 640 mg, and 1280 mg, respectively). All subjects will be on continued stable co-medication with methotrexate (MTX).
详细描述
The trial comprises a screening phase (4 to 12 weeks prior to first administration of veltuzumab), a 4-week treatment phase (weeks 1 to 4), a core phase from week 4 to week 24, and a follow-up phase from week 24 to week 48. The primary end-point, the American College of Rheumatology 20 (ACR 20) response rate, will be evaluated at week 24.
The objectives of this trial are:
- To investigate the efficacy, safety and tolerability at week 24 of three different sc dose levels of the humanized anti-CD20 antibody veltuzumab as an add-on treatment to MTX compared to MTX alone in subjects with moderate to severe RA
- To evaluate the durability of the clinical response and safety of veltuzumab over 48 weeks
- To identify the dosage(s) of veltuzumab with the most favourable benefit-risk profile to be further evaluated in the subsequent phase II/III clinical program in subjects with moderate to severe RA.
Current status of the trial: Following the voluntary temporary halt of the VELVET dose range finding trial, the sponsor has decided to redesign the protocol and start a new trial as soon as possible.
All patients treated prior to the voluntary halt have completed their safety assessments. It was decided to terminate the VELVET trial and consequently not to recommence enrollment.
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
- Double (Participant, Investigator)
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
- •Active disease defined as:
- •Diagnosis of RA using the ACR criteria for the classification of RA for at least 6 months prior to trial entry (Screening, Visit 1)
- •Swollen joint count (SJC) ≥ 6 and tender joint count (TJC) ≥ 6 referred to as the 66/68 - joint count system
- •High sensitivity C-reactive protein (hs-CRP) ≥ 15 mg/L and/or an erythrocyte sedimentation rate (ESR) ≥ 28 mm/hour
- •Positive rheumatoid factor (RF) ≥ 14 IU/mL and/or anti-cyclic citrullinated protein (CCP) ≥ 20 U
- •An inadequate response (insufficient initial or loss of response and/or intolerance to at least one administration of these agents) to previous or current treatment with either MTX alone or MTX plus anti-tumour necrosis factor alpha (anti-TNFα) biological treatment. Subjects should not have received more than two different anti-TNFα therapies.
- •Receiving MTX 15-25 mg/week (oral or parenteral) for at least 20 weeks, including the last 6 weeks prior to Baseline (Visit 3, Day 1) at a stable dose via the same route of administration and formulation. A stable dose of 12.5 mg of MTX is acceptable if the MTX dose has been reduced for reasons of toxicity, e.g. pulmonary, hepatic or haematological toxicity. MTX co-medication will be continued until the end of the trial (Week 48)
排除标准
- •Primary or secondary immunodeficiency including HIV infection
- •Evidence of acute or chronic infection with hepatitis B and C virus (HBV and HCV)
- •Evidence (e.g. chest X-ray [posterior-anterior view], tuberculin/ PPD skin test, etc., according local guidelines) and/or history of active tuberculosis (TB), prior to successfully completing an anti-TB treatment. X-rays performed prior to inclusion (Screening, Visit 1) into the trial are accepted provided they were done within 3 months prior to Screening (Visit 1). Subjects with latent TB infection (LTBI) can be included
- •Significant cardiac disease or history of severe COPD
- •Diabetes mellitus type 1 or unstable type 2
- •History of cancer within the last 5 years treated with anti-cancer chemotherapy
研究组 & 干预措施
Veltuzumab 80 mg
干预措施: Veltuzumab (Drug)
Veltuzumab 160 mg
干预措施: Veltuzumab (Drug)
Veltuzumab 320 mg
干预措施: Veltuzumab (Drug)
Placebo
干预措施: Veltuzumab (Drug)
结局指标
主要结局
American College of Rheumatology 20 (ACR20) response rate at completion of week 24
时间窗: 24 weeks
ACR20 response rate is defined as improvement from baseline to endpoint fulfilling the following criteria: * ≥ 20 percent reduction in the Tender joint count (TJC) (66/68 joint count system) * ≥ 20 percent reduction in the Swollen joint count (SJC) (66/68 joint count system) * ≥ 20 percent reduction in three of the following additional measures: * Patient's assessment of pain * Patient's global assessment of disease activity * Physician's global assessment of disease activity * Degree of disability * Level of acute-phase reactant (CRP)
次要结局
- ACR50/70 response rate(24 and 48 weeks)
- ACR20 response rate(48 weeks)
- Further efficacy analyses (Hybrid ACR response, DAS28-CRP, EULAR response)(24 and 48 weeks)