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.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
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.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
研究連絡先
- 名前:Ralph DeFronzo, MD
- 電話番号:210 567 6692
- メール:defronzo@uthscsa.edu
研究連絡先のバックアップ
- 名前:Eugene Feigin, PhD
- 電話番号:210 567 6707
- メール:feigin@uthscsa.edu
研究場所
-
-
Texas
-
San Antonio、Texas、アメリカ、78229
- University of Texas Health Science Center at San Antonio
-
コンタクト:
- Ralph DeFronzo, MD
- 電話番号:210-567-6691
- メール:defronzo@uthscsa.edu
-
コンタクト:
- Andrea Hansis-Diarte, MPH
- 電話番号:210-567-3208
- メール:hansisdiarte@uthscsa.edu
-
San Antonio、Texas、アメリカ、78229-3900
- Texas Diabetes Institute/UH
-
コンタクト:
- Ralph DeFronzo, MD
- 電話番号:210-358-7200
- メール:defronzo@uthscsa.edu
-
主任研究者:
- Ralph DeFronzo, MD
-
コンタクト:
- Andrea Hansis-Diarte, MPh
- 電話番号:210-567-3208
- メール:hansisdiarte@uthscsa.edu
-
-
参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
-
Age between 18 and 75 years.
-
Males or females
-
HbA1c between 7.5% and 10.5%
-
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
-
No changes in diabetes medications in the 4 weeks prior to enrollment.
-
Estimated glomerular filtration rate (eGFR) ≥ 30 ml/min/1.73m².
-
Blood pressure lower than 170/110 mmHg.
-
Abnormal dexamethasone suppression test: morning plasma cortisol >1.8 µg/dL with plasma dexamethasone ≥140 ng/dL.
-
Self-reported stable (within ±6 lbs in the last 3 months) body weight and body mass index (BMI) between 25-40 kg/m².
-
Negative Glutamic Acid Decarboxylase (GAD) antibody.
-
Hematocrit ≥ 34%.
-
Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) ≤ 3× the upper limit of normal.
-
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的: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.
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
HbA1c (measure of average blood sugar over 3 months) levels
時間枠: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
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in Beta-cell funtion
時間枠: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
時間枠:Baseline to 24 weeks
|
Measured by DEXA scan |
Baseline to 24 weeks
|
|
Liver and visceral fat
時間枠:Baseline to 24 weeks
|
Measured using MRI PDFF (magnetic resonance imaging-proton density fat fraction) |
Baseline to 24 weeks
|
|
Liver stiffness
時間枠:Baseline to 24 weeks
|
Assessed using Fibroscan |
Baseline to 24 weeks
|
|
Change in insulin sensitivity
時間枠:Baseline to 20-24 weeks
|
Assessed using the Oral glucose tolerance test |
Baseline to 20-24 weeks
|
協力者と研究者
スポンサー
スポンサー
協力者
協力者
捜査官
捜査官
- 主任研究者:Ralph DeFronzo, MD、The University of Texas Health Science Center at San Antonio
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- STUDY00002401
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
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 共有時間枠
After study completion and data analysis
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。