- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07570810
Efficacy, Safety, and Tolerability of CS0159 Combined With Semaglutide in MAFLD Patients With Obesity and T2DM
1 maggio 2026 aggiornato da: 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).
Panoramica dello studio
Stato
Non ancora reclutamento
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Interventistico
Iscrizione (Stimato)
30
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Yifei Zhang
- Numero di telefono: +86-13524640378
- Email: feifei-a@163.com
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
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.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Triplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore attivo: 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).
|
|
Comparatore 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).
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Percentage change in body weight relative to baseline
Lasso di tempo: 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
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Change in patient's weight relative to the baseline
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 giugno 2026
Completamento primario (Stimato)
30 novembre 2026
Completamento dello studio (Stimato)
31 dicembre 2026
Date di iscrizione allo studio
Primo inviato
15 marzo 2026
Primo inviato che soddisfa i criteri di controllo qualità
1 maggio 2026
Primo Inserito (Effettivo)
6 maggio 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
6 maggio 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
1 maggio 2026
Ultimo verificato
1 maggio 2026
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie del sistema endocrino
- Disturbi della nutrizione
- Malattie metaboliche
- Ipernutrizione
- Peso corporeo
- Malattie dell'apparato digerente
- Disturbi del metabolismo del glucosio
- Diabete mellito
- Malattie del fegato
- Sovrappeso
- Fegato grasso
- Condizioni patologiche, segni e sintomi
- Malattie nutrizionali e metaboliche
- Segni e sintomi
- Obesità
- Diabete mellito, tipo 2
- Malattia del fegato grasso non alcolica
- semaglutide
Altri numeri di identificazione dello studio
- MAFLD-CS0159-IIT-E
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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