- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07570810
Efficacy, Safety, and Tolerability of CS0159 Combined With Semaglutide in MAFLD Patients With Obesity and T2DM
1. maj 2026 opdateret af: 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).
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
30
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Yifei Zhang
- Telefonnummer: +86-13524640378
- E-mail: feifei-a@163.com
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Tredobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: 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).
|
|
Placebo komparator: 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).
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage change in body weight relative to baseline
Tidsramme: 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
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in patient's weight relative to the baseline
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. juni 2026
Primær færdiggørelse (Anslået)
30. november 2026
Studieafslutning (Anslået)
31. december 2026
Datoer for studieregistrering
Først indsendt
15. marts 2026
Først indsendt, der opfyldte QC-kriterier
1. maj 2026
Først opslået (Faktiske)
6. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
6. maj 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
1. maj 2026
Sidst verificeret
1. maj 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Sygdomme i det endokrine system
- Ernæringsforstyrrelser
- Metaboliske sygdomme
- Overernæring
- Kropsvægt
- Sygdomme i fordøjelsessystemet
- Glukosemetabolismeforstyrrelser
- Diabetes mellitus
- Leversygdomme
- Overvægtig
- Fed lever
- Patologiske tilstande, tegn og symptomer
- Ernæringsmæssige og metaboliske sygdomme
- Tegn og symptomer
- Fedme
- Diabetes mellitus, type 2
- Ikke-alkoholisk fedtleversygdom
- Semaglutid
Andre undersøgelses-id-numre
- MAFLD-CS0159-IIT-E
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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