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A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ZKLJ02 Injection in Healthy Chinese Research Participants (ZKLJ02-I)

A Randomized, Double-blind, Placebo-controlled, Dose-escalation Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Intravenous Administration of ZKLJ02 Injection in Healthy Chinese Research Participants

A randomized, double-blind, placebo-controlled, dose-escalation Phase I clinical study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single intravenous administration of ZKLJ02 injection in healthy Chinese research participants

調査の概要

研究の種類

介入

入学 (実際)

50

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

    • Yunnan
      • Kunming、Yunnan、中国
        • Yunnan Zhongke Longjin Biotechnology Co.,Ltd.

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:

  1. Able to provide informed consent and willing to comply with the study procedures;
  2. Age between 18 and 45 years (inclusive), regardless of gender;
  3. No clinically significant past or current medical history of cardiovascular, hepatic, renal, gastrointestinal, neurological, respiratory, psychiatric, or metabolic disorders, as determined by the investigator;
  4. Physical examination, laboratory tests, 12-lead ECG, and vital signs are all normal or show abnormalities that are not clinically significant;
  5. Body mass index (BMI) between 19.0 and 26.0 kg/m^2 (inclusive); body weight not less than 50 kg for males and not less than 45 kg for females;
  6. Men with reproductive potential and women of childbearing potential must have no plans for pregnancy, sperm donation, or oocyte donation from the time of informed consent until 30 days after the final study visit, and must agree to use effective contraception.

Exclusion Criteria:

  1. Individuals with a history of definite drug or food allergy, or known allergic reaction to any component of this product;
  2. Known or suspected malignant tumors;
  3. History of unexplained syncope, symptomatic hypotension, or hypoglycemia;
  4. History or family history of long QT interval syndrome, or ECG showing QTcF >= 450 ms in males or >= 470 ms in females;
  5. History of chronic diarrhea, malabsorption, unexplained weight loss, or food intolerance;
  6. Individuals with a history of intracranial hemorrhage (e.g., after traffic accidents), stroke, or cerebrovascular disease;
  7. Any disease (e.g., acute gastritis, gastrointestinal ulcers, gastrointestinal bleeding, Henoch-Schönlein purpura, systemic lupus erythematosus, etc.) or medical history (e.g., coagulation disorders, history of intracranial hemorrhage, history of intraocular hemorrhage, history of hemophilia, history of von Willebrand disease, etc.) that, in the investigator's judgment, could alter or increase the tendency to bleed;
  8. Regular and continuous use within 3 months prior to screening of medications affecting coagulation function (e.g., clopidogrel, ticlopidine, dipyridamole, warfarin-like anticoagulants, novel oral anticoagulants such as rivaroxaban, apixaban, etc.), or prior treatment with anticoagulants such as heparin, low-molecular-weight heparin, or fibrinolytic agents;
  9. Presence of significant factors affecting normal venipuncture, such as history of heparin allergy, history of heparin-induced thrombocytopenia, inability to tolerate venipuncture, or history of needle or blood phobia;
  10. Positive test results for human immunodeficiency virus (HIV) antibody, hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, or syphilis antibody;
  11. Blood donation or blood loss of more than 500 mL within 3 months prior to screening;
  12. Participation in any other drug or medical device clinical trial within 3 months prior to screening, or currently participating in another clinical trial, or still within five half-lives of an investigational medicinal product at the time of screening;
  13. Use of any prescription medication, over-the-counter drug, or dietary supplement within 14 days or five half-lives (whichever is longer) prior to the first administration of the study drug;
  14. Hospitalization or major surgery within 6 months prior to screening;
  15. History of drug abuse within 9 months prior to screening;
  16. Individuals with a history of alcoholism or regular alcohol consumption within 9 months prior to screening, defined as more than 14 alcohol units per week (14 units = 8 bottles of beer (500 mL each, 3.5% alcohol content) or 500 g of baijiu (45% alcohol content) or 1.5 bottles of wine (750 mL each, 13% alcohol content)), or those unwilling to abstain from alcohol during the study period;
  17. Study participants who smoked more than 5 cigarettes per day in the past 6 months, or used tobacco-containing alternative products in equivalent amounts, or who cannot ensure complete abstinence from smoking during the study period;
  18. Pregnant or lactating women, those with a positive pregnancy test result, and female study participants who engaged in unprotected sexual activity within 2 weeks prior to the start of screening;
  19. Onset of acute illness during the screening phase or prior to the first administration of study medication;
  20. Consumption within 48 hours before dosing of any food or beverage containing caffeine, alcohol, xanthine, or grapefruit components (e.g., coffee, strong tea, chocolate, etc.);
  21. Positive breath alcohol test result or positive drug abuse screening result;
  22. Any individual with special dietary requirements who cannot comply with the standardized diet (e.g., intolerance to standard meals, lactose intolerance, etc.);
  23. Other conditions deemed by the investigator as unsuitable for participation in this study.

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:他の
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:ダブル

武器と介入

参加者グループ / アーム
介入・治療
実験的:用量群 1
Dissolve 10 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
実験的:用量群 2
Dissolve 20 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
実験的:用量群 3
Dissolve 40 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
実験的:用量グループ 4
Dissolve 80 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.
実験的:用量グループ 5
Dissolve 120 mg of ZKLJ02 for injection or placebo in 250 ml of 0.9% sodium chloride injection and administer intravenously over 2 hours ± 10 minutes within 1 hour before medication; the ratio of study participants receiving ZKLJ02 for injection to placebo is 8:2.

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
Adverse Event
時間枠:Within 24 hours of administering the experimental drug
The incidence rate of adverse events, severity and nature of adverse events, correlation between adverse events and investigational products
Within 24 hours of administering the experimental drug

二次結果の測定

結果測定
時間枠
Maximum Observed Plasma Concentration (Cmax)
時間枠:Within 8 hours of administering the experimental drug
Within 8 hours of administering the experimental drug
Area Under the Plasma Concentration Time Curve (AUC)
時間枠:Within 8 hours of administering the experimental drug
Within 8 hours of administering the experimental drug
Time to the Maximum Plasma Concentration (Tmax)
時間枠:Within 8 hours of administering the experimental drug
Within 8 hours of administering the experimental drug
Activated Partial Thromboplastin Time (APTT)
時間枠:Within 24 hours of administering the experimental drug
Within 24 hours of administering the experimental drug
Prothrombin Time (PT)
時間枠:Within 24 hours of administering the experimental drug
Within 24 hours of administering the experimental drug
Thrombin Time (TT)
時間枠:Within 24 hours of administering the experimental drug
Within 24 hours of administering the experimental drug
Incidence rate of antidrug antibody (ADA)
時間枠:Within 7 days of administering the experimental drug
Within 7 days of administering the experimental drug

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11日

一次修了 (実際)

2025年11月18日

研究の完了 (実際)

2025年11月18日

試験登録日

最初に提出

2026年5月18日

QC基準を満たした最初の提出物

2026年6月5日

最初の投稿 (実際)

2026年6月10日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月10日

QC基準を満たした最後の更新が送信されました

2026年6月5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

追加の関連 MeSH 用語

その他の研究ID番号

  • YunnanZhongkeLongjinBio
  • ChiCTR2500111786 (その他の識別子:Chinese Clinical Trial Registry (ChiCTR))

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

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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