评估 Ianalumab 在系统性红斑狼疮患者中的长期安全性的 3 期扩展研究(SIRIUS-SLE 扩展)。 (SIRIUS-SLE LTE)
A Randomized, Double-blind, Placebo-controlled Extension Study, Followed by a Study Treatment Withdrawal or Open-label Period, to Assess the Long-term Safety and Tolerability of Ianalumab in Patients With Systemic Lupus Erythematosus (SIRIUS-SLE Extension)
The purpose of this study is to evaluate long-term safety and tolerability of ianalumab in participants with systemic lupus erythematosus who have previously completed the treatment period in one of the two SIRIUS-SLE core studies (CVAY736F12301 or CVAY736F12302).
研究概览
详细说明
The purpose of this extension study is to evaluate long-term safety and tolerability of ianalumab administered s.c. monthly or quarterly, compared to monthly placebo, in adolescent and adult participants with anti-nuclear antibody (ANA)-positive systemic lupus erythematosus of moderate-to-severe disease activity, who have completed either CVAY736F12301 (SIRIUS-SLE 1) or CVAY736F12302 (SIRIUS-SLE 2) core studies.
This extension study will last up to 7 years and includes the following three treatment periods:
- a 3-year double-blind, randomized, placebo-controlled treatment period, evaluating the safety and efficacy of ianalumab or placebo (Period 1);
- followed by a 2-year treatment period evaluating safety and efficacy of treatment withdrawal and open-label ianalumab administered s.c. monthly.
- and an up to 2-year open-label, safety monitoring period (Period 3).
研究类型
注册 (估计的)
阶段
- 第三阶段
扩展访问
联系人和位置
学习联系方式
- 姓名:Novartis Pharmaceuticals
- 电话号码:1-888-669-6682
- 邮箱:novartis.email@novartis.com
研究联系人备份
- 姓名:Novartis Pharmaceuticals
- 电话号码:+41613241111
- 邮箱:novartis.email@novartis.com
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Alabama
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Anniston、Alabama、美国、36207
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- Pinnacle Research Group Llc
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接触:
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- 电话号码:+1 256 236 0055
- 邮箱:rfields@pinnacletrials.com
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California
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Burbank、California、美国、91505
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首席研究员:
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接触:
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- 电话号码:+1 818 869 7067
- 邮箱:Sandra.Figueroa@providence.org
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La Palma、California、美国、90623
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接触:
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Westlake Village、California、美国、91361
- 主动,不招人
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Colorado
-
Aurora、Colorado、美国、80045
- 招聘中
- University of Colorado Denver
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首席研究员:
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接触:
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- 邮箱:chong.pedrick@cuanschutz.edu
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Florida
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Clearwater、Florida、美国、33765
- 招聘中
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首席研究员:
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接触:
- Jessica Mayfield
- 电话号码:+1 727 466 0078
- 邮箱:JMayfield@crwf.com
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Cooper City、Florida、美国、33024
- 招聘中
- GNP Research
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首席研究员:
- Mark Jaffe
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接触:
- Melissa Pierce
- 电话号码:+1 754 248 3589
- 邮箱:melissa@gnpresearch.com
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Homestead、Florida、美国、33033
- 招聘中
- Homestead Assoc In Research Inc
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首席研究员:
- Gilberto Seco
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接触:
- Mario Hernandez
- 电话号码:13052460873
- 邮箱:mhernandez@associatesinresearch.com
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Plantation、Florida、美国、33324
- 招聘中
- IRIS Research and Development
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首席研究员:
- Guillermo Valenzuela
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接触:
- Jhon Galindo
- 电话号码:+1 954 476 2338
- 邮箱:jgalindo@irisrheumatology.com
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Tampa、Florida、美国、33603
- 招聘中
- Clinical Research of West Florida Inc
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首席研究员:
- John Carter
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接触:
- Abby Carlson
- 电话号码:+1 813 870 1292
- 邮箱:ACarlson@crwf.com
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Georgia
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Lawrenceville、Georgia、美国、30044
- 招聘中
- Parris and Associates Rheumatology
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首席研究员:
- Glenn Parris
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接触:
- Mannai Coutermarsh
- 电话号码:+17709621616#8334
- 邮箱:m.coutermarsh@parrisandassociates.net
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Illinois
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Skokie、Illinois、美国、60076
- 完全的
- Robert A Hozman MD SC
-
Willowbrook、Illinois、美国、60527
- 招聘中
- Willow Rheumatology Wellness
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首席研究员:
- Angela R Crowley
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接触:
- Lubna Ali
- 邮箱:lali@willowrheum.com
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Louisiana
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Lake Charles、Louisiana、美国、70601
- 招聘中
- Accurate Clinical Research
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首席研究员:
- Enrique Mendez
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接触:
- Machell Broussard
- 邮箱:mbroussard@accurateclinicalresearch.com
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New Orleans、Louisiana、美国、70112
- 主动,不招人
- UMC New Orleans
-
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Maryland
-
Baltimore、Maryland、美国、21201
- 主动,不招人
- University Of Maryland
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Michigan
-
Detroit、Michigan、美国、48202
- 招聘中
- Henry Ford Health
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首席研究员:
- Alireza Meysami
-
接触:
- Jenna Hudy
- 电话号码:+1 313 916 1984
- 邮箱:jhudy1@hfhs.org
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Grand Blanc、Michigan、美国、48439
- 招聘中
- Ahmed Arif Medical Research Center
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首席研究员:
- Ali Karrar
-
接触:
- Iman Abdelrahman
- 电话号码:+1 810 953 8700
- 邮箱:iman@aamrc.net
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Ohio
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Middleburg Heights、Ohio、美国、44130
- 招聘中
- Paramount Med Rsrch and Consult LLC
-
首席研究员:
- Isam Diab
-
接触:
- Denine Ryan
- 电话号码:+1 440 891 9395
- 邮箱:deniner64@gmail.com
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Pennsylvania
-
Pittsburgh、Pennsylvania、美国、15213
- 招聘中
- University Of Pittsburgh
-
首席研究员:
- Andreea Coca
-
接触:
- Kathryn Lemon
- 邮箱:kal128@pitt.edu
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Tennessee
-
Jackson、Tennessee、美国、38305
- 招聘中
- West Tennessee Research Institute
-
首席研究员:
- Jacob A Aelion
-
接触:
- Rachel Williams
- 电话号码:17316330119
- 邮箱:rwilliams@arthritisclinic.org
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Memphis、Tennessee、美国、38119
- 招聘中
- Shelby Research LLC
-
首席研究员:
- Ramesh C Gupta
-
接触:
- Suvarna Konangula
- 电话号码:+1 901 681 9670
- 邮箱:shelbyres1999@outlook.com
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Texas
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Bellaire、Texas、美国、77401
- 招聘中
- Novel Research LLC
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首席研究员:
- Wajeeha Yousaf
-
接触:
- Hassan Khan
- 邮箱:khan@novelresearch.net
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League City、Texas、美国、77573
- 招聘中
- Accurate Clinical Research
-
首席研究员:
- Sabeen Najam
-
接触:
- Mariela Martinez
- 电话号码:+1 281 422 7179
- 邮箱:mmartinez@accurateclinicalresearch.com
-
Red Oak、Texas、美国、75154
- 招聘中
- Epic Medical Research
-
首席研究员:
- Sunny Patel
-
接触:
- Harshini Potluri
- 电话号码:+1 469 206 2642
- 邮箱:hpotluri@epicmedresearch.com
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-
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-
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Braga、葡萄牙、4710-243
- 招聘中
- Novartis Investigative Site
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Lisbon、葡萄牙、1050-034
- 招聘中
- Novartis Investigative Site
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-
-
-
-
Barcelona、西班牙、08035
- 招聘中
- Novartis Investigative Site
-
Madrid、西班牙、28034
- 招聘中
- Novartis Investigative Site
-
Valencia、西班牙、46014
- 招聘中
- Novartis Investigative Site
-
-
A Coruna
-
Santiago Compostela、A Coruna、西班牙、15706
- 招聘中
- Novartis Investigative Site
-
-
Barcelona
-
Badalona、Barcelona、西班牙、08916
- 招聘中
- Novartis Investigative Site
-
-
Cantabria
-
Santander、Cantabria、西班牙、39008
- 招聘中
- Novartis Investigative Site
-
-
Catalonia
-
Barcelona、Catalonia、西班牙、08003
- 招聘中
- Novartis Investigative Site
-
-
Madrid
-
San Sebastian Reyes、Madrid、西班牙、28702
- 招聘中
- Novartis Investigative Site
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-
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Caba、阿根廷、C1015ABO
- 主动,不招人
- Novartis Investigative Site
-
Caba、阿根廷、C1427CCL
- 招聘中
- Novartis Investigative Site
-
San Miguel de Tucumán、阿根廷、T4000AXL
- 主动,不招人
- Novartis Investigative Site
-
-
Buenos Aires
-
La Plata、Buenos Aires、阿根廷、B1900AWT
- 招聘中
- Novartis Investigative Site
-
Quilmes、Buenos Aires、阿根廷、1878
- 招聘中
- Novartis Investigative Site
-
San Miguel、Buenos Aires、阿根廷、B1663GKT
- 主动,不招人
- Novartis Investigative Site
-
-
Tucumán Province
-
San Miguel、Tucumán Province、阿根廷、T4000CBC
- 主动,不招人
- Novartis Investigative Site
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Gwangju、韩国、61469
- 招聘中
- Novartis Investigative Site
-
Seoul、韩国、06591
- 招聘中
- Novartis Investigative Site
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Seoul、韩国、04763
- 招聘中
- Novartis Investigative Site
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Perak
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Ipoh、Perak、马来西亚、30450
- 招聘中
- Novartis Investigative Site
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Key Inclusion Criteria:
- Signed informed consent prior to participation in the extension study. Parent or legal guardian's signed informed consent and child's assent, if appropriate, are required before any assessment is performed for participants <18 years of age. Of note, if the participant reaches age of consent (age as per local law) during the study, they will also need to sign the corresponding study Informed Consent Form (ICF) at the next study visit.
- Participants must have participated in either one of the two SIRIUS-SLE core studies, CVAY736F12301 or CVAY736F12302, and have completed the treatment period through Week 60 without treatment discontinuation.
- In the judgement of the investigator, participants must be expected to clinically benefit from continued study treatment.
Key Exclusion Criteria:
- Use of prohibited therapies.
- Active viral, bacterial or other infections requiring intravenous or intramuscular treatment for clinically significant infection which in the opinion of the investigator will place the participant at risk for participation.
- Plans for administration of live vaccines during the study period.
- Pregnant or nursing (lactating) women.
Other protocol-defined inclusion/exclusion criteria may apply.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Ianalumab monthly
Ianalumab s.c. monthly |
Ianalumab s.c. monthly Ianalumab s.c. quarterly
其他名称:
|
|
实验性的:Ianalumab quarterly
Ianalumab s.c. quarterly |
Ianalumab s.c. monthly Ianalumab s.c. quarterly
其他名称:
|
|
安慰剂比较:Placebo monthly
Placebo s.c. monthly |
Placebo s.c. monthly |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of treatment-emergent Adverse events/Serious Adverse events
大体时间:through study completion, up to approximately 324 weeks
|
Assessment of long-term safety and tolerability of ianalumab |
through study completion, up to approximately 324 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Proportion of participants who achieved Systemic Lupus Erythematosus Responder Index -4 (SRI-4) response
大体时间:up to Week 324
|
SRI-4 response is defined as:
|
up to Week 324
|
|
Proportion of participants who achieved Definition of Remission in SLE (DORIS) response
大体时间:up to Week 324
|
DORIS is defined as:
|
up to Week 324
|
|
Change in Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index
大体时间:up to Week 324
|
SLICC/ACR Damage Index is a measure of cumulative damage due to SLE |
up to Week 324
|
|
Average daily dose of corticosteroids administered
大体时间:up to Week 324
|
Evaluating the effect of ianalumab on corticosteroids intake |
up to Week 324
|
|
Annualized BILAG moderate or severe flare rate
大体时间:up to Week 324
|
Annualized BILAG moderate or severe flare rate where moderate BILAG flare is defined as 2 or more new BILAG-2004 B items, and severe BILAG flare is defined as 1 or more new BILAG-2004 A items, compared to the previous visit |
up to Week 324
|
|
Ianalumab serum concentrations during treatment and follow-up after last dose
大体时间:up to Week 324
|
To characterize the Pharmacokinetics (PK) of ianalumab |
up to Week 324
|
|
Incidence and titer of anti-ianalumab antibodies in serum (ADA assay) over time.
大体时间:up to Week 324
|
To characterize the immunogenicity of ianalumab |
up to Week 324
|
合作者和调查者
调查人员
- 研究主任:Novartis Pharmaceuticals、Novartis Pharmaceuticals
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- CVAY736F12301E1
- 2023-505929-14-00 (注册表标识符:EU CT NUMBER)
- 2023 (美国 NIH 拨款/合同)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Novartis is committed to sharing access to patient-level data and supporting clinical documents from eligible studies with qualified external researchers. Requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to protect the privacy of patients who have participated in the trial in line with applicable laws and regulations.
This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.