Comparative Clinical Trial of Pharmacokinetics and Pharmacodynamics of Human Insulin Injection
2026年5月27日 更新者:Zhuhai United Laboratories Co., Ltd.
A Single-Center, Randomized, Double-Blind, Two-Formulation, Single-Dose, Two-Period Crossover Clinical Trial Comparing Pharmacokinetics and Pharmacodynamics of Human Insulin Injection
A study of Clinical Trial Comparing Pharmacokinetics and Pharmacodynamics of Human Insulin Injection,in Wuhan Pulmonary Hospital (Wuhan Tuberculosis Prevention and Control Institute).To compare the pharmacokinetic and pharmacodynamics properties of a single subcutaneous dose of the human insulin injection (USLIN®R, Zhuhai United Laboratories (Zhongshan) Co., Ltd.) with the reference product (Novolin®R, Novo Nordisk Inc.) in healthy male subjects,and to evaluate the safety, tolerability, and immunogenicity of the test formulation versus the reference formulation in healthy male subjects.This single-center, randomized, double-blind, two-formulation, single-dose, two-period crossover study will enroll 32 healthy male subjects randomized 1:1 into two sequence groups (A/B, group A is administered in the sequence of T-R, while group B is in R-T).
To evaluate the pharmacokinetic and pharmacodynamic properties of the test preparation and the control preparation in healthy male subjects.
Each subject will receive single doses of both test and reference formulations across two periods (with ≥14-day washout), following the predefined sequence allocation table.
After completing period 2 pharmacokinetic blood sampling, subjects will administer assigned insulin TID for two consecutive days to assess test-reference immunogenicity differences.
調査の概要
研究の種類
介入
入学 (実際)
32
段階
- フェーズ 1
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。
研究場所
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Hubei
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Wuhan、Hubei、中国、430000
- 28 Baofeng Road, Qiaokou District
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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
- 大人
健康ボランティアの受け入れ
はい
説明
Inclusion Criteria:
- Age: 18 to 55 years old (inclusive of 18 and 55 years).
- Gender: Male.
- Body Weight: Not less than 55.0 kg for men, with a body mass index [BMI = weight (kg) / height² (m²)] between 18.0 and 29.0 kg/m² (inclusive of boundary values).
- Vital Signs: Systolic blood pressure ≥90 mmHg and <140 mmHg, diastolic blood pressure ≥60 mmHg and <90 mmHg, pulse rate ≥60 beats/min and ≤100 beats/min, body temperature (forehead) between 36.0°C and 37.3°C, with final judgment by the investigator.
- Glucose Tolerance: Normal glucose tolerance (fasting plasma glucose (FPG) <6.10 mmol/L and >3.50 mmol/L, and 2-hour postprandial blood glucose in oral glucose tolerance test (OGTT) <140 mg/dL (7.78 mmol/L)), glycated hemoglobin value <6.3% and >4.5%.
Exclusion Criteria:
- Those who have participated in a clinical trial of another drug/device and used the investigational drug/device within 6 months.
- Those with clinically significant abnormal conditions requiring exclusion, including but not limited to neurological, cardiovascular, hematologic and lymphatic, immune, renal, hepatic, gastrointestinal, respiratory, metabolic, and skeletal system disorders, particularly those with a history of hypoglycemia, hypokalemia, postural hypotension, syncope or blackout, diabetes mellitus, or a family history (first-degree relatives) of diabetes mellitus.
- Those with a history of severe vomiting, diarrhea, or any other disease or condition that could interfere with trial results within 7 days prior to the trial.
- Those with a history of specific allergies (e.g., asthma, urticaria, eczema) or allergies to any medications, foods, or pollen, or known allergies to insulin.
- Those with positive anti-insulin antibodies.
- Those who have lost or donated more than 400 mL of blood, received blood transfusions, or used blood products within 3 months prior to the trial, or who plan to donate blood during the trial.
- Subjects with plans for childbearing or sperm donation from 2 weeks prior to the trial to 6 months after the last dose, and who are unwilling or unable to use effective contraception.
- Those with clinically significant abnormalities in general physical examination, laboratory tests (blood routine, blood biochemistry, coagulation function, urine routine, etc.) within 7 days prior to the trial, or electrocardiogram results deemed clinically significant by the clinician within 14 days prior to the trial.
- Those with one or more clinically significant positive results for hepatitis B, hepatitis C, HIV, or syphilis tests.
- Those who have undergone surgery within 3 months prior to the trial, plan to undergo surgery during the study, or have had surgery that affects drug absorption, distribution, metabolism, or excretion.
- Those who consumed more than 14 units of alcohol per week within 3 months prior to the trial (1 unit = 17.7 mL ethanol, i.e., 354 mL of 5% alcohol beer, 44 mL of 40% alcohol liquor, or 147 mL of 12% alcohol wine), or those unable to abstain from alcohol during the trial.
- Those who smoked an average of more than 5 cigarettes per day within 3 months prior to the trial, or those unable to stop using any tobacco-based or nicotine products (e.g., nicotine patches, chewing gums) during the trial.
- Those who consumed excessive amounts of tea, coffee, and/or caffeine-rich beverages (more than 8 cups, 1 cup = 250 mL) per day within 3 months prior to the trial.
- Those who consumed any food or beverage rich in caffeine/xanthine or other special ingredients (e.g., strong tea, coffee, chocolate, cola, animal offal, grapefruit, grapefruit juice, dragon fruit, mango) from screening to 2 days before admission, which, in the investigator's judgment, may affect drug absorption, distribution, metabolism, or excretion, or those unable to stop consuming such foods or beverages by the end of drug administration.
- Those who used any drugs that alter liver enzyme activity within 28 days prior to the trial (common liver enzyme inducers: barbiturates (phenobarbital being the most common), carbamazepine, aminoglutethimide, griseofulvin, meprobamate, phenytoin, glutethimide, rifampicin, dexamethasone; common liver enzyme inhibitors: chlorpromazine, cimetidine, ciprofloxacin, metronidazole, chloramphenicol, sulfonamides).
- Those who used any drugs affecting insulin's glucose-lowering effects within 28 days prior to the trial (e.g., corticosteroids, danazol, diazoxide, diuretics, epinephrine, salbutamol, terbutaline, glucagon, growth hormone, thyroid hormone, beta-blockers).
- Those unable to eat, with swallowing difficulties, special dietary requirements, or unable to follow a standardized diet.
- Those who used any prescription drugs, over-the-counter drugs, nutraceuticals, herbal products, or vaccines within 14 days prior to the trial.
- Those engaged in hazardous mechanical operations, such as working at heights or driving motor vehicles.
- Those unable to tolerate venipuncture or with a history of hemophobia or needle phobia.
- Those with a history of asthma or seizures.
- Those with a history of hereditary galactose intolerance, lactase deficiency, or glucose-galactose malabsorption.
- ;Those who used any illicit drugs within one year prior to the trial.
- Those with a positive alcohol breath test or positive drug abuse screening.
- Subjects deemed by the investigator to have poor treatment compliance or any factors making participation in this trial inappropriate.
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:ヘルスサービス研究
- 割り当て:ランダム化
- 介入モデル:クロスオーバー割り当て
- マスキング:トリプル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:グループA
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a single subcutaneous dose of 0.3 IU/kg
a single subcutaneous dose of 0.3 IU/kg
|
|
アクティブコンパレータ:グループB
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a single subcutaneous dose of 0.3 IU/kg
a single subcutaneous dose of 0.3 IU/kg
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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 |
|---|---|---|
|
Primary PK Parameters (Peak Plasma Concentration (Cmax))
時間枠:0 to 12 hours
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PK Parameters (Peak Plasma Concentration (Cmax))
|
0 to 12 hours
|
|
Primary PK Parameters (Area under the plasma concentration-time curve from time 0 to time τ(AUC0-τ))
時間枠:0 to 12 hours
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Area under the plasma concentration-time curve from time 0 to time τ(AUC0-τ)
|
0 to 12 hours
|
|
Primary PD Parameters (Area under the glucose infusion rate curve from time 0 to time τ(AUCGIR0-τ))
時間枠:0 to 12 hours
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Area under the glucose infusion rate curve from time 0 to time τ(AUCGIR0-τ)
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0 to 12 hours
|
|
Primary PD Parameters (Maximum glucose infusion rate (GIRmax))
時間枠:0 to 12 hours
|
Maximum glucose infusion rate (GIRmax)
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0 to 12 hours
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Secondary PK Parameters (Area under the plasma concentration-time curve from time 0 to time 2 hours(AUC0-2h))
時間枠:0 to 2 hours
|
Area under the plasma concentration-time curve from time 0 to time 2 hours(AUC0-2h)
|
0 to 2 hours
|
|
Secondary PK Parameters (Area under the plasma concentration-time curve from time 0 extrapolated to infinity(AUC0-∞))
時間枠:0 to 12 hours
|
Area under the plasma concentration-time curve from time 0 extrapolated to infinity(AUC0-∞)
|
0 to 12 hours
|
|
Secondary PK Parameters (Time to maximum (peak) plasma concentration(Tmax))
時間枠:0 to 12 hours
|
Time to maximum (peak) plasma concentration(Tmax)
|
0 to 12 hours
|
|
Secondary PK Parameters (Terminal elimination rate constant(λz))
時間枠:0 to 12 hours
|
Terminal elimination rate constant(λz)
|
0 to 12 hours
|
|
Secondary PK Parameters (Elimination half-life(t1/2))
時間枠:0 to 12 hours
|
Elimination half-life(t1/2)
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0 to 12 hours
|
|
Secondary PD Parameters (Area under the glucose infusion rate curve from time 0 to 2 hours(AUCGIR0-2h))
時間枠:0 to 2 hours
|
Area under the glucose infusion rate curve from time 0 to 2 hours(AUCGIR0-2h)
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0 to 2 hours
|
|
Secondary PD Parameters (Time to reach maximum glucose infusion rate(TGIRmax))
時間枠:0 to 12 hours
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Time to reach maximum glucose infusion rate(TGIRmax)
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0 to 12 hours
|
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Secondary PD Parameters (Time to onset of action,Tonset)
時間枠:0 to 12 hours
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Time to onset of action,Tonset
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0 to 12 hours
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Immunogenicity Assessment (Anti-drug antibody (ADA) incidence (positive rate))
時間枠:0 to 12 hours
|
Anti-drug antibody (ADA) incidence (positive rate)
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0 to 12 hours
|
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Immunogenicity Assessment (ADA titers (for positive samples))
時間枠:0 to 12 hours
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ADA titers (for positive samples)
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0 to 12 hours
|
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。
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 (実際)
2025年8月4日
一次修了 (実際)
2025年11月25日
研究の完了 (実際)
2026年1月13日
試験登録日
最初に提出
2026年5月5日
QC基準を満たした最初の提出物
2026年5月19日
最初の投稿 (実際)
2026年5月27日
学習記録の更新
投稿された最後の更新 (実際)
2026年6月1日
QC基準を満たした最後の更新が送信されました
2026年5月27日
最終確認日
2026年5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
- PD-INS-PK-PD355
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
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