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Efficacy, Safety and Cardiovascular Protection of Mazdutide in Type 1 Diabetes

5 november 2026 uppdaterad av: Linong Ji, Peking University People's Hospital

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.

Studieöversikt

Status

Har inte rekryterat ännu

Betingelser

Studietyp

Interventionell

Inskrivning (Beräknad)

182

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

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Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  1. Age ≥18 years at screening.

  2. Patients with a clinical diagnosis of T1D for at least 12 months.

    Patients with T1D must satisfy all three of the following features:

    1. Clinical diagnosis of type 1 diabetes by a specialist physician;
    2. 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;
    3. 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).
  3. Willingness to use once-weekly mazdutide.

  4. HbA1c ≥7.0% and <10.0%.

  5. Body mass index (BMI) ≥20 kg/m².

  6. 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:

    1. Multiple daily injections of basal insulin plus prandial insulin;
    2. Premixed insulin analog injected 2-3 times daily;
    3. Dual insulin analog (insulin degludec/aspart) injected twice daily;
    4. 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].
  7. 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:

  1. Other types of diabetes.
  2. BMI <20 kg/m².
  3. History of cardiovascular disease: previous myocardial infarction, unstable angina, coronary revascularization (PCI or CABG), stroke, transient ischemic attack (TIA), or symptomatic peripheral arterial disease.
  4. Renal impairment: estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m² (based on the CKD-EPI equation).
  5. Hepatic disease: known severe hepatic disease, or ALT/AST levels >3 times the upper limit of normal.
  6. Personal or family history of medullary thyroid carcinoma, or multiple endocrine neoplasia syndrome type 2.
  7. Pancreatic disease: history of acute or chronic pancreatitis.
  8. Pregnancy and lactation: women who are pregnant, breastfeeding, or planning pregnancy and unwilling to use effective contraception.
  9. 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.
  10. Requirement for long-term use of systemic glucocorticoids (topical/inhaled use permitted).
  11. History of hypersensitivity to GLP-1 receptor agonists, mazdutide, or any of its excipients.
  12. Moderate or more severe non-proliferative diabetic retinopathy or proliferative diabetic retinopathy.
  13. 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

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Fyrdubbla

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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-jämförare: 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

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Proportion of the participants achieving time in range (TIR)>70 and time below range (TBR)<4% (TIMES-EFFICACY)
Tidsram: 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)
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Level of HbA1c
Tidsram: 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
Tidsram: 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
Tidsram: 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)
Tidsram: From baseline to 52 weeks

Changes in TIR (%) from baseline to Week 52

From baseline to 52 weeks
Time above range (TAR)
Tidsram: From baseline to 52 weeks

Changes in TAR (%) from the baseline to Week 52

From baseline to 52 weeks
Time below range (TBR)
Tidsram: From baseline to 52 weeks

Changes in TBR (%) from baseline to Week 52

From baseline to 52 weeks
Covariation (CV)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: From baseline to 52 weeks

Changes in HDL-C (mmol/L) from baseline to Week 52

From baseline to 52 weeks

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
The level of urinary albumin/creatinine ratio
Tidsram: 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
Tidsram: 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
Tidsram: From baseline to Week 52

Changes in inflammation-related protein biomarkers (assessed by Olink) from baseline to Week 52

From baseline to Week 52

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 januari 2027

Primärt slutförande (Beräknad)

1 mars 2029

Avslutad studie (Beräknad)

1 juni 2029

Studieregistreringsdatum

Först inskickad

20 oktober 2026

Först inskickad som uppfyllde QC-kriterierna

5 november 2026

Första postat (Faktisk)

9 november 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

9 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

5 november 2026

Senast verifierad

1 november 2026

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

IPD-planbeskrivning

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.

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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