- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07924553
Efficacy, Safety and Cardiovascular Protection of Mazdutide in Type 1 Diabetes
Type 1 Diabetes Intervention With Mazdutide for Efficacy, Safety and Cardiovascular Protection (The TIMES Trial Program-TIMES-EFFICACY & TIMES-CV
This study is a multicenter, randomized, double-blind, placebo-controlled clinical trial in patients with type 1 diabetes (T1D), conducted in two stages.
Stage 1 is the efficacy and safety assessment (TIMES-EFFICACY). A total of 182 T1D patients who meet the inclusion criteria will be randomized in a 1:1 ratio to two groups: one receiving mazdutide and the other receiving placebo. The follow-up period is 16 weeks. The primary clinical endpoint is the proportion of patients achieving time in range (TIR) >70% with time below range (TBR) <4%. An interim analysis will be performed at Week 8; if the absolute TBR in the mazdutide group increases by more than 5% relative to the placebo group, the subsequent study will be terminated.
Stage 2 is the cardiovascular protective effect assessment (TIMES-CV). During the Stage 1 efficacy and safety assessment, a pre-specified stratification method will ensure that 104 patients with high cardiovascular risk factors are randomized in a 1:1 ratio to the mazdutide group or the placebo group. After completing the 16-week efficacy and safety assessment, these 104 subjects will continue to receive randomized controlled treatment and enter the cardiovascular effect assessment stage, with a total follow-up duration of 52 weeks. The primary clinical endpoint is the change in non-calcified coronary artery plaque volume.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Chu Lin, M.D.
- Telefonnummer: +86 18811792075
- E-post: chulin@bjmu.edu.cn
Studer Kontakt Backup
- Navn: Xiaoling Cai, M.D.
- Telefonnummer: +86 13051396340
- E-post: dr_junel@sina.com
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
-
Age ≥18 years at screening.
-
Patients with a clinical diagnosis of T1D for at least 12 months.
Patients with T1D must satisfy all three of the following features:
- Clinical diagnosis of type 1 diabetes by a specialist physician;
- Any one of the following: age at onset <15 years; no overweight or obesity at onset; diabetic ketoacidosis at onset; peak stimulated C-peptide <200 pmol/L;
- Any one of the following: continuous insulin therapy since diagnosis (excluding pancreas or islet transplantation); one or more positive pancreatic islet autoantibodies (GADA / IAA / IA-2A / ZnT8).
-
Willingness to use once-weekly mazdutide.
-
HbA1c ≥7.0% and <10.0%.
-
Body mass index (BMI) ≥20 kg/m².
-
Continuous use of any of the following insulin regimens for at least 3 months prior to screening (no concomitant use of other oral glucose-lowering drugs or GLP-1RAs allowed), with a stable insulin dose for at least 2 weeks before enrollment:
- Multiple daily injections of basal insulin plus prandial insulin;
- Premixed insulin analog injected 2-3 times daily;
- Dual insulin analog (insulin degludec/aspart) injected twice daily;
- Continuous subcutaneous insulin infusion (CSII). Note: A stable insulin dose is defined as a daily insulin dose adjustment of no more than ±[value not specified in the source document].
-
Ability to provide informed consent prior to any study-related activity.
- For participants enrolled in TIMES-CV, in addition to the above criteria, the following criteria must also be met: ***
1. Duration of type 1 diabetes ≥5 years. 2. Moderate or high 10-year atherosclerotic cardiovascular disease (ASCVD) risk (≥5.0%) as assessed by the China-PAR model.
3. Carotid atherosclerotic plaque confirmed by ultrasound.
Exclusion Criteria:
- Other types of diabetes.
- BMI <20 kg/m².
- History of cardiovascular disease: previous myocardial infarction, unstable angina, coronary revascularization (PCI or CABG), stroke, transient ischemic attack (TIA), or symptomatic peripheral arterial disease.
- Renal impairment: estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m² (based on the CKD-EPI equation).
- Hepatic disease: known severe hepatic disease, or ALT/AST levels >3 times the upper limit of normal.
- Personal or family history of medullary thyroid carcinoma, or multiple endocrine neoplasia syndrome type 2.
- Pancreatic disease: history of acute or chronic pancreatitis.
- Pregnancy and lactation: women who are pregnant, breastfeeding, or planning pregnancy and unwilling to use effective contraception.
- Medications: use of GLP-1 receptor agonists, GIP or GCG receptor agonists, other non-insulin glucose-lowering drugs, or finerenone within 3 months prior to screening.
- Requirement for long-term use of systemic glucocorticoids (topical/inhaled use permitted).
- History of hypersensitivity to GLP-1 receptor agonists, mazdutide, or any of its excipients.
- Moderate or more severe non-proliferative diabetic retinopathy or proliferative diabetic retinopathy.
- Any other serious medical or psychiatric condition that, in the judgment of the investigator, may interfere with study assessments or endanger the safety of the subject.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: mazdutide group
Participants in the treatment group will receive mazdutide by subcutaneous injection once weekly. The dose will be escalated stepwise according to a pre-defined regimen from a safe starting dose to an effective maintenance dose (from 2 mg to 4 mg) over several weeks, with dose reduction permitted if needed. |
Mazdutide is a synthetic peptide analog of mammalian oxyntomodulin and a once-weekly dual agonist of the glucagon-like peptide-1 receptor (GLP-1R) and the glucagon receptor (GCGR), under development for the treatment of obesity and type 2 diabetes (T2D). Mazdutide has been shown to induce significant weight loss in patients with obesity and to help improve glycemic control in patients with T2D. |
|
Placebo komparator: placebo group
Participants in the control group will receive a placebo matched to mazdutide in appearance, packaging, and mode of administration, by subcutaneous injection once weekly. |
mazdutide matching placebo |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Proportion of the participants achieving time in range (TIR)>70 and time below range (TBR)<4% (TIMES-EFFICACY)
Tidsramme: From baseline to 16 weeks
|
The proportion of adult patients with T1D achieving the composite outcome of continuous glucose monitoring (CGM)-measured TIR >70% and TBR <4% at Week 16 in the mazdutide group versus the placebo group |
From baseline to 16 weeks
|
|
Volume of non-calcified coronary artery plaque (TIMES-CV)
Tidsramme: From baseline to 52 weeks
|
The absolute change in non-calcified coronary artery plaque volume in mm³ from baseline to Week 52, as measured by quantitative analysis of high-resolution coronary computed tomography angiography (CCTA) |
From baseline to 52 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Level of HbA1c
Tidsramme: From baseline to 52 weeks
|
Changes in HbA1c (%) from baseline to Week 16 and Week 52 |
From baseline to 52 weeks
|
|
Volume of coronary atherosclerotic plaque
Tidsramme: From baseline to 52 weeks
|
Changes in total coronary atherosclerotic plaque volume, fibrous plaque volume, low-density plaque volume, and lipid-rich plaque volume in mm³ |
From baseline to 52 weeks
|
|
Thickness of carotid intima-media
Tidsramme: From baseline to 52 weeks
|
Changes in carotid intima-media thickness (cIMT) in mm from baseline to Week 52 |
From baseline to 52 weeks
|
|
Time in range (TIR)
Tidsramme: From baseline to 52 weeks
|
Changes in TIR (%) from baseline to Week 52 |
From baseline to 52 weeks
|
|
Time above range (TAR)
Tidsramme: From baseline to 52 weeks
|
Changes in TAR (%) from the baseline to Week 52 |
From baseline to 52 weeks
|
|
Time below range (TBR)
Tidsramme: From baseline to 52 weeks
|
Changes in TBR (%) from baseline to Week 52 |
From baseline to 52 weeks
|
|
Covariation (CV)
Tidsramme: From baseline to 52 weeks
|
Changes in CV (%) assessed by continuous glucose monitoring from baseline to Week 52 |
From baseline to 52 weeks
|
|
Level of triglyceride (TG)
Tidsramme: From baseline to 52 weeks
|
Changes in TG (mmol/L) from baseline to Week 52 |
From baseline to 52 weeks
|
|
Level of total cholesterol (TC)
Tidsramme: From baseline to 52 weeks
|
Changes in TC (mmol/L) from baseline to Week 52 |
From baseline to 52 weeks
|
|
Level of low-density cholesterol (LDL-C)
Tidsramme: From baseline to 52 weeks
|
Changes in LDL-C (mmol/L) from baseline to Week 52 |
From baseline to 52 weeks
|
|
Level of high-density cholesterol (HDL-C)
Tidsramme: From baseline to 52 weeks
|
Changes in HDL-C (mmol/L) from baseline to Week 52 |
From baseline to 52 weeks
|
Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
The level of urinary albumin/creatinine ratio
Tidsramme: From baseline to 52 weeks
|
Changes in urinary albumin/creatinine ratio (mg/g) from baseline to Week 52 |
From baseline to 52 weeks
|
|
Change in hepatic fat content
Tidsramme: From baseline to 52 weeks
|
Changes in hepatic fat content (%) from baseline to Week 52, assessed by MRI-PDFF |
From baseline to 52 weeks
|
|
Levels of inflammation-related protein biomarkers
Tidsramme: From baseline to Week 52
|
Changes in inflammation-related protein biomarkers (assessed by Olink) from baseline to Week 52 |
From baseline to Week 52
|
Samarbeidspartnere og etterforskere
Samarbeidspartnere
Publikasjoner og nyttige lenker
Generelle publikasjoner
- Pasqua MR, Tsoukas MA, Kobayati A, Aboznadah W, Jafar A, Haidar A. Subcutaneous weekly semaglutide with automated insulin delivery in type 1 diabetes: a double-blind, randomized, crossover trial. Nat Med. 2025 Apr;31(4):1239-1245. doi: 10.1038/s41591-024-03463-z. Epub 2025 Jan 10.
- Guo L, Zhang B, Xue X, Zhang X, Cai H, Jiang H, Zhang L, Jin P, Wang X, Cheng Z, Zhang S, Geng J, Guo Y, Hu H, Ma Q, Li L, Du H, Han-Zhang H, Xue F, Deng H, Qian L, Yang W; DREAMS-2 investigators. Mazdutide versus dulaglutide in Chinese adults with type 2 diabetes. Nature. 2026 Apr;652(8108):181-188. doi: 10.1038/s41586-025-10031-z. Epub 2025 Dec 17.
- Zhu D, Zhao J, Cai H, Chu X, Xiu S, Song C, Cheng Z, Cao H, Jiang H, Zhang L, Wang H, Shi B, Li Y, Liu M, Feng B, Xue F, Deng H, Li H, Li L, Li Y, Ma Q, Qian L. Mazdutide versus placebo in Chinese adults with type 2 diabetes. Nature. 2026 Apr;652(8108):174-180. doi: 10.1038/s41586-025-10026-w. Epub 2025 Dec 17.
- Gao L, Jiang H, Cai H, Tian J, Shi B, Qiu W, Huang C, Han J, Zhang S, Pang S, Bi Y, Chen L, Gu X, Han J, Ma Q, Deng H, Wang Y, Li L, Han-Zhang H, Qian L, Ji L; GLORY-2 Trial Investigators. Treatment With 9-mg Mazdutide for Weight Reduction in Chinese Adults With Obesity: The GLORY-2 Randomized Clinical Trial. JAMA. 2026 Aug 4;336(5):377-388. doi: 10.1001/jama.2026.8142.
- Ji L, Jiang H, Bi Y, Li H, Tian J, Liu D, Zhao Y, Qiu W, Huang C, Chen L, Zhong S, Han J, Zhang Y, Lian Q, Yang P, Lv L, Gu J, Liu Z, Deng H, Wang Y, Li L, Pei L, Qian L; GLORY-1 Investigators. Once-Weekly Mazdutide in Chinese Adults with Obesity or Overweight. N Engl J Med. 2025 Jun 12;392(22):2215-2225. doi: 10.1056/NEJMoa2411528. Epub 2025 May 25.
- Shirley M. Mazdutide: First Approval. Drugs. 2025 Dec;85(12):1621-1627. doi: 10.1007/s40265-025-02249-y. Epub 2025 Sep 30.
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2026PHD024-004
- 3-SRA-2026-1955-M-B (Annet stipend/finansieringsnummer: Breakthrough T1D)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
There is no plan to make individual participant data (IPD) collected in this study available to researchers outside the primary research group. The study data will be kept confidential by the sponsor and investigators in accordance with applicable regulations and the study protocol. Sharing of IPD is not planned due to considerations regarding participant confidentiality and data protection.
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .