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.
Aperçu de l'étude
Statut
Statut
Les conditions
Les conditions
Intervention / Traitement
Intervention / Traitement
Description détaillée
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.
Type d'étude
Type d'étude
Inscription (Estimé)
Inscription
Phase
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
Coordonnées de l'étude
- Nom: Ralph DeFronzo, MD
- Numéro de téléphone: 210 567 6692
- E-mail: defronzo@uthscsa.edu
Sauvegarde des contacts de l'étude
- Nom: Eugene Feigin, PhD
- Numéro de téléphone: 210 567 6707
- E-mail: feigin@uthscsa.edu
Lieux d'étude
-
-
Texas
-
San Antonio, Texas, États-Unis, 78229
- University of Texas Health Science Center at San Antonio
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Contact:
- Ralph DeFronzo, MD
- Numéro de téléphone: 210-567-6691
- E-mail: defronzo@uthscsa.edu
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Contact:
- Andrea Hansis-Diarte, MPH
- Numéro de téléphone: 210-567-3208
- E-mail: hansisdiarte@uthscsa.edu
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San Antonio, Texas, États-Unis, 78229-3900
- Texas Diabetes Institute/UH
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Contact:
- Ralph DeFronzo, MD
- Numéro de téléphone: 210-358-7200
- E-mail: defronzo@uthscsa.edu
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Chercheur principal:
- Ralph DeFronzo, MD
-
Contact:
- Andrea Hansis-Diarte, MPh
- Numéro de téléphone: 210-567-3208
- E-mail: hansisdiarte@uthscsa.edu
-
-
Critères de participation
Critère d'éligibilité
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
-
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
-
No changes in diabetes medications in the 4 weeks prior to enrollment.
-
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
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Nombre de bras
Armes et Interventions
Groupe de participants / BrasGroupe de participants / Bras |
Intervention / TraitementIntervention / Traitement |
|---|---|
|
Expérimental: 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.
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
HbA1c (measure of average blood sugar over 3 months) levels
Délai: 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
|
Mesures de résultats secondaires
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in Beta-cell funtion
Délai: 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
Délai: Baseline to 24 weeks
|
Measured by DEXA scan |
Baseline to 24 weeks
|
|
Liver and visceral fat
Délai: Baseline to 24 weeks
|
Measured using MRI PDFF (magnetic resonance imaging-proton density fat fraction) |
Baseline to 24 weeks
|
|
Liver stiffness
Délai: Baseline to 24 weeks
|
Assessed using Fibroscan |
Baseline to 24 weeks
|
|
Change in insulin sensitivity
Délai: Baseline to 20-24 weeks
|
Assessed using the Oral glucose tolerance test |
Baseline to 20-24 weeks
|
Collaborateurs et enquêteurs
Parrainer
Parrainer
Collaborateurs
Collaborateurs
Les enquêteurs
Les enquêteurs
- Chercheur principal: Ralph DeFronzo, MD, The University of Texas Health Science Center at San Antonio
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Début de l'étude
Achèvement primaire (Estimé)
Achèvement primaire
Achèvement de l'étude (Estimé)
Achèvement de l'étude
Dates d'inscription aux études
Première soumission
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Première publication
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour publiée
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies du système endocrinien
- Maladies métaboliques
- Troubles du métabolisme du glucose
- Diabète sucré
- Hyperinsulinisme
- Maladies des glandes surrénales
- Hyperfonction corticosurrénalienne
- Maladies nutritionnelles et métaboliques
- Diabète sucré, Type 2
- Résistance à l'insuline
- Syndrome de Cushing
- fracas
Autres numéros d'identification d'étude
Autres numéros d'identification d'étude
- STUDY00002401
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
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.
Délai de partage IPD
After study completion and data analysis
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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