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治験 NCT03940183（対象：2型糖尿病）は完了です。詳細は治験レーダーのタイル表示と AI 発見ツールで確認するか、ここで質問してください。 | ||
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Clinical Trial of Trelagliptin Succinate Tablets in the Treatment of Type 2 Diabetes 第III相・フェーズ3 254 無作為化 二重盲検 プラセボ対照
治験（臨床試験）の詳細は主に英語で提供されていますが、治験レーダーAIがサポートします！「治験解説」をクリックして、選択した言語で試験情報を表示し、議論してください。
治験番号 NCT03940183 は 治療 の研究で、2型糖尿病 を対象とした 第III相・フェーズ3 介入研究 臨床試験 でした。現在は 完了 です。2019年7月8日 に開始し、254 名の参加者 が参加しました。この試験は CSPC ZhongQi Pharmaceutical Technology Co., Ltd. によって主導され、2020年12月28日 に完了しました。ClinicalTrials.gov からの最新更新日は 2021年1月12日 です。
概要
The trial used a randomized, double-blind, placebo-controlled, superior-effect design, multicenter clinical study.
The trial was divided into a test group and a placebo group,the two groups were randomized in a 1:1 ratio and planned to enroll 240 patients with type 2 diabetes. After 2 weeks of screening, all subjects entered the treatment period,which was 24 weeks, and 1 week period of follow-up.
詳細説明
The trial was divided into a test group and a placebo group: the test group was given trelagliptin succinate tablets, and the placebo group was given placebo. The test group and the placebo group were randomized in a 1:1 ratio and planned to enroll 240 patients with type 2 diabetes. After 2 weeks of screening, all subjects entered the treatment period,which was 24 weeks, and 1 week period of follow-up.
All subjects ...
もっと見る公式タイトル
A Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Trial of Trelagliptin Succinate Monotherapy for Type 2 Diabetes
疾患名
2型糖尿病その他の研究識別子
- CSPC/HC1425/201801
NCT番号
開始日
2019-07-08
最終更新日
2021-01-12
終了予定日
2020-12-28
目標参加者数
254
試験の種類
介入研究
治験の相・段階
第III相・フェーズ3
状況
完了
キーワード
type 2 diabetes
monotherapy
trelagliptin succinate
monotherapy
trelagliptin succinate
主目的
治療
割付方法
無作為化
介入モデル
並行割当
盲検化
四重盲検
群（アーム）／介入
| 参加グループ/群 | 介入/治療法 |
|---|---|
実験的Trelagliptin succinate 100 mg Tablets,100mg per tablet,oral, once a week, 100mg each time, continuous medication for a total of 24 weeks | Trelagliptin Succinate the experimental group will use trelagliptin succinate 100 mg for 24weeks |
プラセボ対照薬Placebo Oral Tablet Tablets,N/A,oral, once a week, one tablet each time, continuous medication for a total of 24 weeks | プラセボ経口錠 the placebo Comparator groups use placebo oral tablet for 24weeks |
主要評価項目
副次評価項目
| 評価指標 | 指標の説明 | 時間枠 |
|---|---|---|
HbA1c | Changes in HbA1c compared to baseline at week 24 | Baseline, week 24 |
| 評価指標 | 指標の説明 | 時間枠 |
|---|---|---|
HbA1c | Changes in HbA1c compared to baseline at week 16 | Baseline, week 16 |
Fasting blood glucose | Changes in Fasting blood glucose compared to baseline at week 16,week 24 | Baseline, week 16，week 24 |
2-hour postprandial blood glucose | Changes in 2-hour postprandial blood glucose compared to baseline at week 24 | Baseline, week 24 |
fasting insulin | Changes in fasting insulin compared to baseline at week 24 | Baseline, week 24 |
fasting glucagon | Changes in fasting glucagon compared to baseline at week 24 | Baseline, week 24 |
active Glucagon-like peptide-1（GLP-1） level | Changes in active Glucagon-like peptide-1（GLP-1） level compared to baseline at 24 | Baseline, week 24 |
The percentage of HbA1c<6.5% and HbA1c<7% | The percentage of HbA1c\<6.5% and HbA1c\<7% at week 24 | week 24 |
body weight | Changes in body weight（Kg）compared to baseline at week 24 | Baseline, week 24 |
Body Mass Index | Changes in Body Mass Index （kg/m\^2）compared to baseline at week 24 | Baseline, week 24 |
適格基準
対象年齢
成人, 高齢者
試験の最低年齢
18 Years
対象性別
全て
Subjects who fully understand the test content and possible adverse reactions and voluntarily participate in the trial and sign the informed consent form;
Subjects who meet the World Health Organization(WHO) (1999) criteria for the diagnosis and classification criteria for type 2 diabetes;
18 ≤ age ≤ 75 years old, male or female;
One of the following conditions:
- Initially diagnosed type 2 diabetic patients;
- Patients who with type 2 diabetes diagnosed within 2 years of screening period and are treated with single-agent oral hypoglycemic agents until screening, and do not take the medicine regularly for at least 8 weeks (ie, continuous medication for <1 week);
19kg/m^2 ≤ Body Mass Index（BMI ）≤ 35kg/m^2;
7.0% ≤ HbA1c ≤ 10.0%;
Female subjects of childbearing age are negative in pregnancy test;
Female subjects do not have a fertility plan one month before the trial and all the subjects do not have a fertility plan during and one month after the trial.
- Fasting plasma glucose≥13.9mmol/L or a history of severe hypoglycemia (blood sugar below 2.8mmol/L);
- Systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg during screening;
- Positive for Acquired Immure Deficiency Syndrome（AIDS）or syphilis testing;
- Active hepatitis B virus infection or hepatitis C virus infection;
- History of acute or chronic liver disease, and Aspartate aminotransferase(AST) or Alanine minotransferase(ALT)> 2.5 times of reference range or total bilirubin> 1.5 times of reference range during the screening period;
- Renal insufficiency subjects, the serum creatinine above 1.5 times of reference range during the screening period;
- The white blood cells are outside of the reference range, hemoglobin below the reference range, triglyceride>5.7mmol/L during the screening period;
- Acute complications of diabetes (including diabetic ketoacidosis, hyperosmolar nonketotic diabetic coma, lactic acidosis and hypoglycemia coma) ,or severe chronic complications (proliferative diabetic retinopathy, diabetic nephropathy);
- Oral or intravenous use of glucocorticoids or regular application (ie continuous use more than one week within 4 weeks before screening time) with large doses of thiazide diuretics (hydrochlorothiazide, chlorothiazide, etc.);
- Subjects without a pacemaker, the 12-lead ECG showed II or III degree atrioventricular block, long QT syndrome or corrected QT interval （QTc）>450ms or atrial fibrillation during the screening period;
- Active heart disease (including acute myocardial infarction, unstable angina) , moderate to severe congestive heart failure (NYHA class III or IV), or planned for coronary artery bypass grafting or transmyocardial laser revascularization half year before the screening period.
- History of epilepsy, mental illness, major depression,or previous thyroid function abnormal and still being treated, or those with organ transplants, severe chronic lung disease, and other serious heart disease, cerebrovascular disease, blood disease;
- Endocrine diseases such as hypercortisolism or polycystic ovary syndrome that may affect blood glucose levels;
- Inflammatory bowel disease, colon ulcer, partial intestinal obstruction or obvious digestive and dysfunction chronic bowel disease;
- Active pancreatitis, cholecystitis, gallstones and other digestive diseases;
- Using weight loss surgery within 3 months before screening period or using weight-loss drugs (including traditional Chinese medicine diet pills) within2 months before screening period;
- History of drug or drug abuse or alcoholics;
- Blood donation within 2 months before screening includes blood components or massive blood loss (≥400mL),or receiving blood transfusion or using blood products;
- History of allergies with similar drugs (DPP-4 inhibitors) or those who are judged by the investigator to be allergic to the test drug;
- Subjects who are participating in other clinical trials or who have participated in other drug trials within 3 months prior to screening;
- Pregnancy (defined as positive in pregnancy test), lactating women;
- Not suitable for this clinical trial judged by the investigator.
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.連絡先情報がありません。
1 1カ国の場所
Beijing Municipality
Beijing Hospital, Beijing, Beijing Municipality, China