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.
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Chu Lin, M.D.
- 電話番号:+86 18811792075
- メール:chulin@bjmu.edu.cn
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
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
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Age ≥18 years at screening.
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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).
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Willingness to use once-weekly mazdutide.
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HbA1c ≥7.0% and <10.0%.
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Body mass index (BMI) ≥20 kg/m².
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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].
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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.
研究計画
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
|
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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
|
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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
協力者
出版物と役立つリンク
一般刊行物
- 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.
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
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?
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.
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