Platform Trial in Stage 1 Diabetes: Comparing Golimumab vs Placebo
Adaptive Platform Trial to Delay Progression From Normoglycemia to Dysglycemia in Presymptomatic Type 1 Diabetes: Golimumab Substudy
The goal of this clinical trial is to learn if golimumab is effective at preventing progression to Stage 2 diabetes in participants with presymptomatic Type 1 Diabetes. The expected duration of this study is approximately 6 years.
Participants will:
- Take golimumab or placebo injections monthly for the duration of the study or until they are diagnosed with either stage 2 or stage 3 Type 1 Diabetes
- Visit a study clinic every 6 months for Oral Glucose Tolerance Tests (OGTTs) and other tests until the end of the study
研究概览
地位
地位
干预/治疗
干预/治疗
详细说明
研究类型
研究类型
注册 (估计的)
注册
阶段
阶段
- 阶段2
联系人和位置
学习联系方式
学习联系方式
- 姓名:Ariana Rojas
- 电话号码:813-974-6827
- 邮箱:Ariana.Rojas@epi.usf.edu
学习地点
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Massachusetts
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Boston、Massachusetts、美国、02115
- Joslin Diabetes Center
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首席研究员:
- Jason Gaglia, MD
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接触:
- Samantha Kateman
- 电话号码:617-975-8269
- 邮箱:skateman@joslin.harvard.edu
-
-
参与标准
资格标准
资格标准
适合学习的年龄
- 孩子
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Willing to provide informed consent or have a parent or legal guardians provide informed consent when the participant is <18 years of age.
- Weight ≥15 kg at the time of screening.
- Aged ≥2 to <45 years.
- A confirmed history of either IA2A alone or at least two or more diabetes-related biochemical autoantibodies (mIAA, GADA, ICA, IA-2A, ZnT8A) present on the same sample. Confirmed autoantibody result means that the presence of the antibody has been verified on more than one occasion. For multiple autoantibody positivity, the same autoantibodies do not need to be present on the different tests. Confirmation must occur within the six months prior to screening. In the absence of other antibodies, ICA and GADA positivity alone will not suffice for eligibility in this study.
- Oral glucose tolerance test (OGTT) results demonstrating normal glucose tolerance within 7 weeks (52 days) prior to randomization. If a participant has known previous abnormal glucose tolerance, the two most recent OGTTs must demonstrate normal glucose tolerance to be eligible.
- CMV and/or EBV seronegative participants must be CMV and EBV PCR negative within 60 days of randomization and may not have had signs or symptoms of a CMV or EBV-compatible illness lasting longer than 7 days within 30 days of randomization.
- CMV seropositive participants must be CMV PCR negative and all EBV seropositive participants must have EBV PCR < 2,000 IU/mL within 60 days of randomization and may not have had signs or symptoms of a CMV or EBV-compatible illness lasting longer than 7 days within 30 days of randomization.
- Be at least 4 weeks from last live immunization.
- Be willing to forgo live vaccines during treatment and for 3 months after study drug treatment period.
- Must meet TrialNet eligibility minimum immunization recommendations found in Appendix A of the manual of operations (MOO).
- Negative Coccidioides serology testing for those who have in the past resided in for at least 2 months, currently reside in, or within the past 2 months have visited an endemic area (as defined in Protocol MOO Appendix B).
- If a female participant with reproductive potential, willing to avoid pregnancy (abstinence or adequate contraceptive method) through up to 3 months after last study drug administration and undergo pregnancy testing at each study visit.
Exclusion Criteria:
One or more screening laboratory values as stated:
- Leukocytes <3,500/μL or >14,000/μL
- Neutrophils <1,500/mL
- Platelet count <100,000 /μL
- Hemoglobin <6.2 mmol/L (10.0 g/dL)
- AST or ALT ≥ 2 times the upper limits of normal (2x ULN)
Abnormal Glucose Tolerance or Diabetes
- Fasting plasma glucose ≥100 mg/dL (6.1 mmol/L), or
- 2 hour plasma glucose ≥140 mg/dL (7.8 mmol/L), or
- 30, 60, or 90 minute plasma glucose during OGTT ≥200 mg/dL (11.1 mmol/L)
- History of treatment with insulin except transient use during acute illness or hospitalization.
- Vaccination with a live vaccine within the last 4 weeks or killed/inactivated vaccine within the last 2 weeks prior to randomization.
- A history of confirmed infectious mononucleosis within the 3 months prior to randomization, as documented by EBV serology (EBV VCA-IgM and VCA-IgG; PCR would be confirmatory).
Evidence of prior or current tuberculosis (TB) infection through any one or more of the following:
- A history of latent or active TB
- Signs and/or symptoms of TB
- Recent close contact with a person with known or suspected active TB unless appropriate prophylaxis for TB was given
- A history of a chest X-ray consistent with active TB or old, inactive TB
- A history of a positive purified protein derivative (PPD) skin test result (>10 mm induration), or positive/repeatedly indeterminate on an interferon-gamma release assay (IGRA; e.g., QuantiFERON-TB test).
- Prone to infections or has chronic, recurrent or opportunistic infectious disease, including but not limited to Pneumocystis carinii, aspergillosis, latent or active granulomatous infection, or an open, draining, or infected non-healing skin wound or ulcer.
- Known active infection or active signs or symptoms of acute or chronic infection at the time of randomization including SARS-Cov-2.
- Have or had a demyelinating disorder such as multiple sclerosis or Guillain-Barré syndrome.
- Current diagnosis of other autoimmune diseases except stable and/or adequately treated hypothyroidism and/or celiac disease (participants must be well controlled for the previous 6 months).
- Current or ongoing use of non-insulin pharmaceuticals that affect glycemic control within 14 days of the screening visit.
- Has previously participated in a clinical trial for diabetes prevention and received active study agent within 6 months of treatment.
- History of blastomycosis, histoplasmosis, or coccidioidomycosis.
- A history of malignancies other than fully treated basal cell or squamous cell carcinoma of the skin.
- Have or had moderate to severe congestive heart failure.
- Ongoing or anticipated future use of any medications known to impact T1D progression.
- Evidence of current or past HIV or Hepatitis B or current Hepatitis C infection.
- Be pregnant or lactating or anticipate becoming pregnant during the study.
- Any condition, prior treatment, or laboratory abnormality that in the investigator's opinion may adversely affect study participation or confound study results.
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
手臂数量
武器和干预
参与者组/臂参与者组/臂 |
干预/治疗干预/治疗 |
|---|---|
|
实验性的:Golimumab
Participants assigned to this arm will receive golimumab injections
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Golimumab will be given as a subcutaneous formulation based on the participant's weight at baseline.
A loading dose regimen at 0 and 2 weeks will be followed by monthly maintenance doses for the duration of the participant's enrollment in the study.
For those weighing 15kg to less than 40 kg the dosing will be: 100mg (week 0), followed by 50mg monthly thereafter.
For those weighing 40kg or more the loading dose will be 200mg (week 0) followed by 100mg thereafter.
其他名称:
|
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安慰剂比较:Placebo
Participants assigned to this arm will receive saline (placebo) to match Golimumab injections
|
0.9% Sodium Chloride Injection USP ("Normal" saline) is to be dispensed as the placebo for this study.
A loading dose regimen at 0 and 2 weeks will be followed by monthly maintenance doses for the duration of the participant's enrollment in the study.
其他名称:
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研究衡量的是什么?
主要结果指标
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Progression to Dysglycemia
大体时间:From randomization to confirmed dysglycemia or clinical diagnosis of T1D, approximately 6 years from the first participant enrolled.
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The primary outcome is the elapsed time from random treatment assignment to the development of confirmed dysglycemia or overt hyperglycemia/symptomatic based upon ADA criteria.
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From randomization to confirmed dysglycemia or clinical diagnosis of T1D, approximately 6 years from the first participant enrolled.
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次要结果测量
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Progression to overt hyperglycemia/symptomatic Type 1 Diabetes
大体时间:From Randomization to clinical diagnosis approximately 6 years from the first participant enrolled.
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Elapsed time from study drug administration to the development of diabetes or time of last contact among those randomized
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From Randomization to clinical diagnosis approximately 6 years from the first participant enrolled.
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合作者和调查者
调查人员
调查人员
- 学习椅:Jason Gaglia, MD、TrialNet
出版物和有用的链接
有用的网址
研究记录日期
研究主要日期
学习开始 (估计的)
学习开始
初级完成 (估计的)
初级完成
研究完成 (估计的)
研究完成
研究注册日期
首次提交
首次提交
首先提交符合 QC 标准的
首先提交符合 QC 标准的
首次发布 (实际的)
首次发布
研究记录更新
最后更新发布 (实际的)
最后更新发布
上次提交的符合 QC 标准的更新
上次提交的符合 QC 标准的更新
最后验证
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
其他研究编号
- TN39A
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
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
- 国际碳纤维联合会
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
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