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

5. November 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Studientyp

Interventionell

Einschreibung (Geschätzt)

182

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Proportion of the participants achieving time in range (TIR)>70 and time below range (TBR)<4% (TIMES-EFFICACY)
Zeitfenster: 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)
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Level of HbA1c
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: From baseline to 52 weeks

Changes in TIR (%) from baseline to Week 52

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

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

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

Changes in TBR (%) from baseline to Week 52

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

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

From baseline to 52 weeks

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
The level of urinary albumin/creatinine ratio
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: From baseline to Week 52

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

From baseline to Week 52

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Januar 2027

Primärer Abschluss (Geschätzt)

1. März 2029

Studienabschluss (Geschätzt)

1. Juni 2029

Studienanmeldedaten

Zuerst eingereicht

20. Oktober 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. November 2026

Zuerst gepostet (Tatsächlich)

9. November 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

9. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. November 2026

Zuletzt verifiziert

1. November 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

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.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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