- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07570810
Efficacy, Safety, and Tolerability of CS0159 Combined With Semaglutide in MAFLD Patients With Obesity and T2DM
1 mai 2026 mis à jour par: Wang Weiqing, Shanghai Jiao Tong University School of Medicine
A Single -Center, Randomized, Double-blind, Placebo-controlled Proof of Exploratory Study Evaluating the Efficacy, Safety, and Tolerability of CS0159 Combined With Semaglutide in MAFLD Patients With Obesity and T2DM
This is an exploratory study evaluating CS0159 in combination with Semaglutide in metabolic dysfunction-associated fatty liver disease (MAFLD) patients with obesity and type 2 diabetes (T2DM).
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Description détaillée
This is an exploratory study to evaluate the efficacy, safety, and tolerability of CS0159 in combination with Semaglutide in MAFLD patients with obesity and T2DM.
Approximately 30 patients were randomly assigned to two groups in a 1:1 ratio for treatment for 12 weeks.
Type d'étude
Interventionnel
Inscription (Estimé)
30
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Yifei Zhang
- Numéro de téléphone: +86-13524640378
- E-mail: feifei-a@163.com
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
Inclusion Criteria:
- 1. Age≥18 and ≤65 years, male or female.
- 2. MRI-PDFF ≥10% within 3 months prior to randomized.
- 3. Diagnosis of T2DM.
- 4. HbA1c: 7.0%-10.5%.
- 5. FPG: 7.0-13.3 mmol/L.
- 6. BMI: 30-45 kg/m2.
- 7. Subjects control blood glucose only by lifestyle intervention for at least 3 months before the screening period.
- 8. Willing to maintain consistent diet and exercise habits throughout the entire study, and adhere to the study protocol for timely administration of the study drug, and timely self-monitoring of blood glucose and recording.
- 9. Can understand the research content, follow the research protocol, and voluntarily sign the ICF.
Exclusion Criteria:
- 1. ALT≥2.5×ULN, AST≥2.5×ULN, TBil≥2×ULN, creatinine (Cr) ≥1.5×ULN and Serum creatinine clearance<60 mL/min, PLT<100×10^9/L, INR >1.3, ALB <3.5 g/dL.
- 2. Use of glucose-lowering medication in the 3 months prior to randomization.
- 3. Weight loss ≥ 5% in the 3 months prior to randomization or ≥10% in the 6 months prior to randomization or use of other weight-lowering drugs, corticosteroids, and etc.
- 4. History of allergy to glucagon-like peptide-1 receptor agonists (GLP-1RA) medications, currently in an allergic state, having allergic conditions, or history of allergies to ≥2 substances.
- 5. Subjects with T1DM, monogenic diabetes, diabetes caused by pancreatic damage, or other secondary diabetes.
- 6. Subjects with a history of severe pruritus.
- 7. Uncontrolled and potentially unstable diabetic retinopathy or maculopathy.
- 8. Thyroid C-cell tumour or family history, multiple endocrine neoplasia type 2 or family history.
- 9. History of acute or chronic pancreatitis.
- 10. Subjects with Child-Pugh class B or C grade cirrhosis.
- 11. HBsAg positive, HCV Ab positive, HIV Ab positive, TP Ab positive.
- 12. Arrhythmias, male QTc≥450 ms, or female QTc≥470 ms. Or cardiovascular disease for which the researcher has assessed that participation in the trial is not appropriate.
- 13. Diseases that interfere with the absorption, distribution, metabolism or excretion.
- 14. Gastrointestinal diseases that affect food digestion and absorption.
- 15. Use moderate or strong inhibitors or inducers of cytochrome P450 enzyme (CYP3A4 enzyme) within the first 14 days of randomization and throughout the entire trial period.
- 16. History of malignant tumors within the first 5 years of randomization.
- 17. Serious hypoglycemic events occurring ≥ 3 times within 12 weeks prior to administration, or acute and severe metabolic disorder occurred within 12 weeks prior to administration.
- 18. Drug abuse or alcohol abuse within the first 6 months of randomization.
- 19. Poor blood pressure control.
- 20. Mental illness, epilepsy.
- 21. Patients with uncontrollable severe infectious diseases before randomization.
- 22. Pregnant, planned pregnancy or breastfeeding.
- 23. Participated in other clinical trials in the first three months of randomization.
- 24. Any condition that in the judgement of the researcher precludes participation.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Tripler
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur actif: 4mg CS0159
4mg CS0159 (oral, once daily) + 0.5mg Semaglutide (subcutaneous injection, once weekly) for 12 weeks
|
The intervention will include a 12-week treatment period.
During the 12-week treatment period, subjects will receive 4mg CS0159 (oral, once daily).
The intervention will include a 12-week treatment period.
During the 12-week treatment period, subjects will receive 0.5mg Semaglutide (subcutaneous injection, once weekly).
|
|
Comparateur placebo: CS0159 Placebo
CS0159 placebo (oral, once daily) + 0.5mg Semaglutide (subcutaneous injection, once weekly) for 12 weeks
|
The intervention will include a 12-week treatment period.
During the 12-week treatment period, subjects will receive 0.5mg Semaglutide (subcutaneous injection, once weekly).
The intervention will include a 12-week treatment period.
During the 12-week treatment period, subjects will receive CS0159 placebo (oral, once daily).
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Percentage change in body weight relative to baseline
Délai: Baseline to 12 weeks
|
Evaluate the percentage change in body weight relative to baseline after 12 weeks of treatment.
|
Baseline to 12 weeks
|
|
Changes in energy expenditure
Délai: Baseline to 12 weeks
|
The impact of the patient's energy expenditure change relative to the baseline after 12 weeks, assessed by whole-room indirect calorimetry (metabolic chamber).
|
Baseline to 12 weeks
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in patient's weight relative to the baseline
Délai: Baseline to 12 weeks
|
Evaluation of the change in patient's weight relative to the baseline after 12 weeks with CS0159
|
Baseline to 12 weeks
|
|
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Délai: Baseline to 12 weeks
|
Evaluate the safety and tolerability of CS0159 combined with semaglutide during a 12-week treatment period
|
Baseline to 12 weeks
|
|
Change in patient's glucose oxidation
Délai: Baseline to 12 weeks
|
Evaluation of the effect of CS0159 on glucose and lipid oxidation in patients relative to baseline after 12 weeks of administration, assessed by whole-room indirect calorimetry (metabolic chamber).
|
Baseline to 12 weeks
|
|
Change in patient's lipid oxidation
Délai: Baseline to 12 weeks
|
Evaluation of the effect of CS0159 on glucose and lipid oxidation in patients relative to baseline after 12 weeks of administration, assessed by whole-room indirect calorimetry (metabolic chamber).
|
Baseline to 12 weeks
|
|
Percentage change in HbA1c relative to baseline
Délai: Baseline to 12 weeks
|
Evaluate the percentage change in glycated hemoglobin (HbA1c) relative to baseline after 12 weeks of treatment.
|
Baseline to 12 weeks
|
|
Changes relative to baseline in BMI
Délai: Baseline to 12 weeks
|
Changes in body mass index (BMI) relative to baseline after 12 weeks of administration
|
Baseline to 12 weeks
|
|
Changes relative to baseline in body composition
Délai: Baseline to 12 weeks
|
Changes in body composition analysis relative to baseline after 12 weeks of administration
|
Baseline to 12 weeks
|
|
Changes relative to baseline in waist circumference
Délai: Baseline to 12 weeks
|
Changes in waist circumference relative to baseline after 12 weeks of administration
|
Baseline to 12 weeks
|
|
Changes relative to baseline in waist to hip ratio (WHR)
Délai: Baseline to 12 weeks
|
Changes in waist to hip ratio (WHR) relative to baseline after 12 weeks of administration
|
Baseline to 12 weeks
|
|
Changes relative to baseline in serum liver function parameters
Délai: Baseline to 12 weeks
|
including alanine aminotransferase, aspartate aminotransferase, glutamyltransferase, alkaline phosphatase, lactate dehydrogenase, total bilirubin, direct bilirubin, total protein, albumin, and total bile acid.
|
Baseline to 12 weeks
|
|
Changes relative to baseline in serum lipid profile
Délai: Baseline to 12 weeks
|
including serum triglycerides, total cholesterol, low-density lipoprotein cholesterol and high-density lipoprotein cholesterol.
|
Baseline to 12 weeks
|
|
Changes relative to baseline in plasma glucose levels
Délai: Baseline to 12 weeks
|
including fasting plasma glucose and 2-hour post-prandial plasma glucose
|
Baseline to 12 weeks
|
|
Changes relative to baseline in serum insulin levels
Délai: Baseline to 12 weeks
|
including fasting serum insulin and 2-hour post-prandial serum insulin
|
Baseline to 12 weeks
|
|
Changes in peripheral blood metabolomics and proteomics relative to baseline
Délai: Baseline to 12 weeks
|
Changes in peripheral blood metabolomics and proteomics relative to baseline after 12 weeks of administration
|
Baseline to 12 weeks
|
|
Changes in fecal metabolites, gut microbiota homeostasis, and fecal gut microbiota metagenome relative to baseline
Délai: Baseline to 12 weeks
|
Changes in fecal metabolites, gut microbiota homeostasis, and fecal gut microbiota metagenome relative to baseline after 12 weeks of administration
|
Baseline to 12 weeks
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 juin 2026
Achèvement primaire (Estimé)
30 novembre 2026
Achèvement de l'étude (Estimé)
31 décembre 2026
Dates d'inscription aux études
Première soumission
15 mars 2026
Première soumission répondant aux critères de contrôle qualité
1 mai 2026
Première publication (Réel)
6 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
6 mai 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
1 mai 2026
Dernière vérification
1 mai 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies du système endocrinien
- Troubles nutritionnels
- Maladies métaboliques
- Suralimentation
- Poids
- Maladies du système digestif
- Troubles du métabolisme du glucose
- Diabète sucré
- Maladies du foie
- En surpoids
- Foie gras
- Conditions pathologiques, signes et symptômes
- Maladies nutritionnelles et métaboliques
- Signes et symptômes
- Obésité
- Diabète sucré, Type 2
- Stéatose hépatique non alcoolique
- sémaglutide
Autres numéros d'identification d'étude
- MAFLD-CS0159-IIT-E
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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