健康な参加者におけるHRS-1893錠剤の2製剤の生物学的同等性試験
健常参加者におけるHRS-1893錠剤の2製剤の生物学的同等性試験
This study will investigate the bioequivalence between two formulations of HRS-1893 tablets. Safety and tolerability will also be assessed.
調査の概要
研究の種類
入学 (実際)
段階
- フェーズ 1
連絡先と場所
研究場所
-
-
Beijing Municipality
-
Beijing、Beijing Municipality、中国、100730
- Beijing Hospital
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-
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:
- Subjects aged 18 to 55 years (inclusive), regardless of gender;
- Body mass index (BMI) between 19 and 28 kg/m² (inclusive), with body weight ≥ 50.0 kg and < 90.0 kg for men, and ≥ 45.0 kg and < 90.0 kg for women;
- No abnormalities of clinical significance are found upon comprehensive physical examination and laboratory tests, or only minor abnormalities that are deemed by the investigator not to affect the subject's eligibility for enrollment;
- No clinically significant abnormalities on the 12-lead ECG;
- The subject must understand the study procedures and methods, voluntarily agree to participate, and provide written informed consent.
Exclusion Criteria:
- Subjects with suspected hypersensitivity to the investigational drug or any excipient;
- The subject has a history of syncope;
- Exclusion due to blood pressure: Systolic Blood Pressure (SBP) >140 mmHg or <90 mmHg; OR Diastolic Blood Pressure (DBP) >90 mmHg or <60 mmHg, as determined by the investigator to be clinically significant;
- History of gastric or intestinal surgery that, in the investigator's judgment, may affect drug absorption;
- A positive result in any one of the following infectious disease screening tests during the screening period: hepatitis B surface antigen (HBsAg), hepatitis C virus antibody (HCV-Ab), treponema pallidum antibody (syphilis), or human immunodeficiency virus antibody/antigen (HIV-Ab/Ag);
- Subjects who meet any of the following criteria will be excluded: a. Smoking: Average daily cigarette consumption of more than 5 cigarettes within the 4 weeks prior to screening; b. Alcohol: Average daily alcohol intake exceeding 15 g within one week prior to screening (15 g of alcohol is equivalent to 450 mL of beer, 150 mL of wine, or 50 mL of low-alcohol spirits); c. Non-compliance: Inability or unwillingness to abstain from smoking, alcohol, and caffeine-containing foods or beverages during the screening period and the entire study duration; d. Diet: Have special dietary requirements, cannot comply with the standardized diet provided in the study, or have a history of substance abuse;
- History of substance abuse;
- Use of any prescription drugs, over-the-counter medications, or Chinese herbal medicines within 1 month prior to dosing, or the use of any drug within 5 half-lives prior to screening (whichever is longer). Additionally, subjects who plan to take any non-study medications during the trial period will be excluded;
- Any other circumstances that, in the investigator's judgment, make the subject unsuitable for participation in the trial. This includes physiological or psychological conditions that may increase the trial risk, affect the subject's protocol compliance, or impact the subject's ability to complete the study.
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:クロスオーバー割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:HRS-1893試験製剤群
|
Test formulation of HRS-1893 tablet, oral. |
|
実験的:HRS-1893 参照製剤群
|
Reference formulation of HRS-1893 tablet, oral. |
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 |
|---|---|---|
|
Peak concentration (Cmax).
時間枠:From Day 1 to Day 17.
|
Primary Pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 17.
|
|
Area under the plasma concentration - time curve from Time 0 to the last quantifiable time point (AUC0-t).
時間枠:From Day 1 to Day 17.
|
Primary Pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 17.
|
|
Area under the plasma concentration - time curve from Time 0 to infinity (AUC0-∞).
時間枠:From Day 1 to Day 17.
|
Primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 17.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Time to peak concentration (Tmax).
時間枠:From Day 1 to Day 17.
|
Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 17.
|
|
Elimination half-life (t1/2).
時間枠:From Day 1 to Day 17.
|
Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 17.
|
|
Apparent clearance (CL/F).
時間枠:From Day 1 to Day 17.
|
Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 17.
|
|
Apparent volume of distribution (Vz/F).
時間枠:From Day 1 to Day 17.
|
Other primary pharmacokinetic (PK) parameters of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 17.
|
|
Incidence and severity of any adverse events (AEs).
時間枠:From Day 1 to Day 21 ± 2.
|
Safety and tolerability of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 21 ± 2.
|
|
12-Lead Electrocardiogram (ECG) QT Interval.
時間枠:From Day 1 to Day 21 ± 2.
|
Safety and tolerability of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 21 ± 2.
|
|
Transthoracic echocardiogram (TTE) results.
時間枠:From Day 1 to Day 21 ± 2.
|
Safety and tolerability of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 21 ± 2.
|
|
Vital signs results - blood pressure.
時間枠:From Day 1 to Day 21 ± 2.
|
Safety and tolerability of different HRS-1893 formulations in healthy subjects. |
From Day 1 to Day 21 ± 2.
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
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
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