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

2026年11月5日 更新者: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.

調査の概要

状態

まだ募集していません

条件

研究の種類

介入

入学 (推定)

182

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

  • 名前:Xiaoling Cai, M.D.
  • 電話番号:+86 13051396340
  • メール:dr_junel@sina.com

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

プラセボコンパレーター: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

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Proportion of the participants achieving time in range (TIR)>70 and time below range (TBR)<4% (TIMES-EFFICACY)
時間枠: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)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Level of HbA1c
時間枠: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
時間枠: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
時間枠: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)
時間枠:From baseline to 52 weeks

Changes in TIR (%) from baseline to Week 52

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

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

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

Changes in TBR (%) from baseline to Week 52

From baseline to 52 weeks
Covariation (CV)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠:From baseline to 52 weeks

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

From baseline to 52 weeks

その他の成果指標

結果測定
メジャーの説明
時間枠
The level of urinary albumin/creatinine ratio
時間枠: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
時間枠: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
時間枠:From baseline to Week 52

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

From baseline to Week 52

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2027年1月1日

一次修了 (推定)

2029年3月1日

研究の完了 (推定)

2029年6月1日

試験登録日

最初に提出

2026年10月20日

QC基準を満たした最初の提出物

2026年11月5日

最初の投稿 (実際)

2026年11月9日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月9日

QC基準を満たした最後の更新が送信されました

2026年11月5日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2026PHD024-004
  • 3-SRA-2026-1955-M-B (その他の助成金/資金番号:Breakthrough T1D)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

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.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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