Relacorilant in Patients With Poorly Controlled Type 2 Diabetes and Autonomous Cortisol Secretion
The purpose of this study is to assess the effect and effectiveness of Relacorilant on improving the glucose levels in the blood, thus potentially improving glucose control in patients with hard to control diabetes.
This study involves the use of an investigational drug called Relacorilant. "Investigational" means that the drug has not yet been approved by the U.S. Food & Drug Administration (FDA) for treating "mild hypercortisolism" in patients with diabetes. Cortisol is a "stress hormone". The excess production of cortisol can rise blood sugar (glucose) levels and worsen diabetes. Those disturbances might be corrected by the study medication Relacorilant to improve the state of your diabetes.
This study will evaluate the effects of Relacorilant on glucose control and its safety profile. Although the safety of this drug has been tested in prior human research studies, some side effects may not yet be known.
研究概览
详细说明
The objective of the study is to investigate the mechanisms by which glucocorticoid receptor (GR) antagonism with relacorilant improves glucose homeostasis in patients with difficult-to-control type 2 diabetes (T2D) and confirmed endogenous hypercortisolism.
Each patient serves as their own control to assess the mechanistic nature of the study. Comparisons made between pre- and post-treatment outcomes. This within-subject design allows detailed assessment of metabolic changes in response to treatment.
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Ralph DeFronzo, MD
- 电话号码:210 567 6692
- 邮箱:defronzo@uthscsa.edu
研究联系人备份
- 姓名:Eugene Feigin, PhD
- 电话号码:210 567 6707
- 邮箱:feigin@uthscsa.edu
学习地点
-
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Texas
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San Antonio、Texas、美国、78229
- University of Texas Health Science Center at San Antonio
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接触:
- Ralph DeFronzo, MD
- 电话号码:210-567-6691
- 邮箱:defronzo@uthscsa.edu
-
接触:
- Andrea Hansis-Diarte, MPH
- 电话号码:210-567-3208
- 邮箱:hansisdiarte@uthscsa.edu
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San Antonio、Texas、美国、78229-3900
- Texas Diabetes Institute/UH
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接触:
- Ralph DeFronzo, MD
- 电话号码:210-358-7200
- 邮箱:defronzo@uthscsa.edu
-
首席研究员:
- Ralph DeFronzo, MD
-
接触:
- Andrea Hansis-Diarte, MPh
- 电话号码:210-567-3208
- 邮箱:hansisdiarte@uthscsa.edu
-
-
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
Inclusion Criteria:
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Age between 18 and 75 years.
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Males or females
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HbA1c between 7.5% and 10.5%
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Type 2 diabetes with at least one of the following:
- Taking ≥ 3 glucose-lowering drugs
- Taking 2 glucose lowering medication and 2 anti-hypertensive drugs.
- Taking insulin and any other glucose lowering drugs
- Taking ≥ 2 glucose-lowering drugs and presence of microvascular (retinopathy, nephropathy, neuropathy) or ≥ macrovascular (heart attack, heart failure, peripheral vascular disease, atrial fibrillation) disease
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No changes in diabetes medications in the 4 weeks prior to enrollment.
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Estimated glomerular filtration rate (eGFR) ≥ 30 ml/min/1.73m².
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Blood pressure lower than 170/110 mmHg.
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Abnormal dexamethasone suppression test: morning plasma cortisol >1.8 µg/dL with plasma dexamethasone ≥140 ng/dL.
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Self-reported stable (within ±6 lbs in the last 3 months) body weight and body mass index (BMI) between 25-40 kg/m².
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Negative Glutamic Acid Decarboxylase (GAD) antibody.
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Hematocrit ≥ 34%.
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Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) ≤ 3× the upper limit of normal.
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Female participants of childbearing potential must have a negative pregnancy test and agree to use appropriate contraception throughout the study. (Women who are using hormonal contraceptives will need to agree to use an acceptable method of non-hormonal contraception throughout the study and for ≥6 half-lives after the last dose of assigned treatment (7 days prior to randomization).
Exclusion Criteria:
- Diagnosis of type 1 diabetes
- New-onset diabetes of less than 1 year duration.
- Presence of severe acute medical, psychiatric, or surgical illness.
- Use of systemic (oral, IV, intra-articular, or inhaled) or topical glucocorticoids within the past 3 months.
- Use of systemic glucocorticoid during the study is prohibited except in the event of medical emergency OR Requires inhaled glucocorticoid use and may require systemic glucocorticoids if their condition deteriorates during the study
- Night shift workers (unless able to temporarily change sleep schedule to complete dexamethasone test).
- Severe untreated sleep apnea. (Severe untreated sleep apnea, defined as an Apnea-Hypopnea Index (AHI) ≥ 30 events per hour on polysomnography, or a documented clinical diagnosis of severe sleep apnea in patients who are not receiving effective therapy (e.g., CPAP, BiPAP, oral appliance, or surgical treatment).
- Excessive alcohol intake: >14 drinks/week for men or >7 drinks/week for women.
- Diagnosed with or having treatment plans for Cushing syndrome
- Known hypersensitivity to dexamethasone or relacorilant.
- Severe, uncontrolled hypertension (>170/110 mmHg) at screening.
- Use of another investigational drug within 4 weeks or less than 5 half-lives of the compound, whichever is longer.
- Pregnant or lactating women or women of childbearing potential (including all women <50 years old, women whose surgical sterilization was performed <6 months ag; and women who have had a menstrual period in the last 12 months; and women who have a positive pregnancy test before dexamethasone administration.)
- Women with a history of unexplained vaginal bleeding, endometrial hyperplasia with atypia or endometrial carcinoma.
- Diagnosed with or having treatment plans for Cushing syndrome using any of the following treatments: mifepristone, metyrapone, osilodrostat, ketoconazole, fluconazole, aminoglutethimide, etomidate, octreotide, larazotide, pasireotide, long-acting octreotide or pasireotide.
- Uncontrolled thyroid disease (hypo- or hyperthyroidism) prior to first dose of relacorilant as confirmed by TSH outside of normal range (0.4 to 5.0 mIU/L).
- Has plans for adrenalectomy or adrenal nodulectomy during the study period.
- Taking any co-medications that is disallowed with strong CYP3A inhibitors and cannot undergo dose modifications on coadministration with a strong CYP3A inhibitor
- Ongoing use of any strong CYP3A4 inducer
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Study Investigational Drug Group
Participants will receive study intervention once daily after screening and dexamethasone suppression test. |
A capsule that will be given once daily starting at 100mg and increasing gradually to 400mg once a day.
其他名称:
|
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 |
|---|---|---|
|
HbA1c (measure of average blood sugar over 3 months) levels
大体时间:Baseline to 24 weeks
|
Lab test performed on whole blood hemoglobin to determine the blood sugar level over a 3 month period |
Baseline to 24 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in Beta-cell funtion
大体时间:Baseline to 24 weeks
|
Disposition index and C-peptide response during OGTT and euglycemic insulin clamp. |
Baseline to 24 weeks
|
|
Change in total body fat
大体时间:Baseline to 24 weeks
|
Measured by DEXA scan |
Baseline to 24 weeks
|
|
Liver and visceral fat
大体时间:Baseline to 24 weeks
|
Measured using MRI PDFF (magnetic resonance imaging-proton density fat fraction) |
Baseline to 24 weeks
|
|
Liver stiffness
大体时间:Baseline to 24 weeks
|
Assessed using Fibroscan |
Baseline to 24 weeks
|
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Change in insulin sensitivity
大体时间:Baseline to 20-24 weeks
|
Assessed using the Oral glucose tolerance test |
Baseline to 20-24 weeks
|
合作者和调查者
调查人员
- 首席研究员:Ralph DeFronzo, MD、The University of Texas Health Science Center at San Antonio
研究记录日期
研究主要日期
学习开始 (估计的)
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
- STUDY00002401
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
Study participant research data, which is for purposes of statistical analysis and scientific reporting, will be transmitted to and stored at the Diabetes division at UT Health. This will not include the participant's contact or identifying information. Rather, individual participants and their research data will be identified by a unique study identification number.
IPD 共享时间框架
After study completion and data analysis
IPD 共享支持信息类型
- 研究方案
- 树液
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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