BAFF/IL-17 Bispecific Antibody Treatment in Subjects With Primary Sjogren's Syndrome
试验速览
- 阶段
- 2 期
- 状态
- 撤回
- 发起方
- 试验地点
- 1
- 主要终点
- whole unstimulated sialometry
研究概览
简要总结
To demonstrate that tibulizumab (LY3090106) treatment improves the mean unstimulated salivary flow rate or the salivary gland total ultrasound score (TUS) in primary Sjogren's syndrome patients at week 12 compared to the baseline visit.
详细描述
This will be a single-site, open-label study in patients with primary Sjogren's syndrome. All patients will receive tibulizumab (LY3090106) 300mg subcutaneously every 2 weeks for a total of 12 weeks.
Primary Sjogren's syndrome was selected as a relevant patient population based on the mechanism of action of the molecule and the current understanding of the pathogenesis of the disease. An open-label design was chosen based on practical considerations regarding the number of patients that could be recruited. Although open-label studies are subject to bias, objective primary endpoints were intentionally chosen to minimize this concern.
The goal of this study is to demonstrate that tibulizumab (LY3090106) treatment improves the mean unstimulated salivary flow rate or the salivary gland total ultrasound score (TUS) in primary Sjogren's syndrome patients at week 12 compared to the baseline visit.
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 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Men and women 18-85 years of age
- •Confirmed diagnosis of primary Sjogren's syndrome by the 2016 ACR-EULAR classification criteria for primary Sjogren's syndrome
- •All women (regardless of childbearing potential) must test negative for pregnancy at the time of screening
- •Women must also agree to use a reliable method of birth control from screening until 12 weeks following last dose of study drug unless they are not of child bearing potential
- •Have stimulated whole salivary flow rate of greater than or equal to 0.10 ml/minute
- •Have a salivary gland total ultrasound score (TUS) of less than or equal to 9 (on a 0-11 point scale)
排除标准
- •Currently enrolled in a clinical trial involving an investigational product or off-label use of a drug
- •Concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study
- •Have received any nonbiologic investigational product within 30 days or 5 half-lives (whichever is longer) of their baseline (Day 1) visit
- •Have received any biologic investigational product within 3 months or 5 half-lives (whichever is longer) of their baseline visit, or any leukocyte depleting agent within 12 months of baseline
- •Have disease-modifying antirheumatic drug (DMARD) or immunosuppressive use as follows:
- •ANY treatment with a janus kinase (JAK) inhibitor (including but not limited to tofacitinib, baricitinib, upadacitinib, or filgotinib) within 28 days prior to baseline or planned treatment with a JAK inhibitor during the study
- •UNSTABLE PRESCRIBED DOSE of other synthetic DMARDs (eg, hydroxychloroquine, methotrexate, leflunomide, or sulfasalazine) within 28 days prior to baseline or if the dose of drug is planned to be increased during the study (stable prescriptions are allowed)
- •ANY treatment with cytotoxic or immunosuppressive drugs including but not limited to cyclophosphamide, mycophenolic acid, azathioprine, cyclosporine, sirolimus, or tacrolimus within 28 days prior to screening or planned treatment during the study
- •Have had treatment with biologic DMARDs as follows: Etanercept, adalimumab, or anakinra <4 weeks before baseline or planned treatment during the study
- •Have had treatment with biologic DMARDs as follows: Infliximab, certolizumab pegol, golimumab, abatacept, or tocilizumab <8 weeks before baseline or planned treatment during the study
- •Are persons who have previously completed or withdrawn from this study
研究组 & 干预措施
open label
open label study; all subjects will receive the same drug at the same dose
干预措施: tibulizumab (LY3090106) (Drug)
结局指标
主要结局
whole unstimulated sialometry
时间窗: week 12
change in unstimulated salivary flow
salivary gland ultrasound
时间窗: week 12
change in salivary gland ultrasound score
次要结局
- PET(week 12)
- Schirmer I test(week 12)
- ESSDAI(week 12)
- ESSPRI(week 12)
- whole stimulated sialometry(week 12)
- MRI(week 12)
研究者
Matthew C. Baker
Clinical Assistant Professor
Stanford University