健康な被験者および腎機能障害を有する被験者におけるHRS-1301錠の研究
軽度、中等度、重度の腎機能不全を有する被験者および健常被験者におけるHRS-1301錠剤の薬物動態、安全性および薬力学を比較する単回投与、非盲検第I相臨床試験
The primary objective of this study is to evaluate pharmacokinetics of HRS-1301 tablets in subjects with impaired kidney function in comparison with healthy subjects, to develop dose recommendations for patients with renal impairment.
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
-
-
Sichuan
-
Chengdu、Sichuan、中国、610072
- Sichuan Provincial People's Hospital
-
-
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:
- Sign the informed consent before the trial, and fully understand the content, process, and possible adverse reactions of the trial;
- Male or female subjects aged 18 to 65 (including 18 and 65);
- Body mass index (BMI) ranges from 18 kg/m2 to 30 kg/m2 (including 18 and 30),and Male weight ≥ 50.0 kg, female weight ≥ 45.0 kg;
- The glomerular filtration rate should meet the following criteria (GFR, mL/min): Subjects with mild renal impairment: 60-89 mL/min; Subjects with moderate renal impairment: 30-59 mL/min; Subjects with severe renal function impairment: 15~29 mL/min.
Exclusion Criteria:
- Individuals with a specific history of allergies (such as asthma, urticaria, eczema, etc.), or those with an allergic constitution (such as those allergic to any drug or food), or those known to be allergic to any component of the studied drug;
- Those with cardiogenic shock, severe conduction obstruction, sick sinus syndrome, heart failure (NYHA grade III-IV), persistent rapid arrhythmia, tortuous ventricular tachycardia or ventricular tachycardia at the pointed point, a history of clinically significant T-wave changes, myocardial infarction, or angina pectoris;
- Suffering from malignant tumors, or having a history of malignant tumors within 5 years prior to screening (excluding skin non-melanomas that have been treated without recurrence signs and resected cervical intraepithelial neoplasia);
- Those with a history of gastric or intestinal surgery that some researchers believe may affect drug absorption;
- Those who have suffered severe trauma or undergone major surgical operations within the three months prior to screening, or who plan to undergo surgery during the trial period;
- Those who have participated in any clinical trials of drugs or medical devices within three months prior to screening, or those who are still within five half-lives of the drug before screening (whichever is longer);
- Those who have donated blood of ≥ 400 mL within 4 weeks before screening, or have suffered severe blood loss (blood loss ≥ 400 mL), or have received blood transfusion within 8 weeks;
- Those who received live (attenuated) vaccines within 4 weeks prior to screening or those who plan to receive them during the trial;
- Those with potential difficulties in blood collection and a history of fainting at the sight of needles or blood;
- For patients with renal insufficiency,those who have received renal replacement therapy (such as peritoneal dialysis, hemodialysis, etc.) within 3 months prior to the screening or during the expected trial period;
- For patients with renal insufficiency,screening individuals with underlying diseases that induce chronic kidney disease within the previous three months and are judged by researchers to be poorly controlled, such as diabetic patients with HbA1c > 10%, and hypertensive patients with systolic blood pressure > 180 mmHg and diastolic blood pressure > 120 mmHg, etc.
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:なし
- 介入モデル:単一グループの割り当て
- 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-1301 Tablet Group
Treatment for oral medication. |
HRS-1301 tablet, oral medication. |
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 |
|---|---|---|
|
Maximum concentration (Cmax).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
|
Area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC0-last).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
|
Area under the concentration-time curve from time zero to infinity (AUC0-inf).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Time of maximum concentration (Tmax).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
|
Area under the concentration-time curve from time zero to the end of the dosing interval tau (AUC0-tau).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
|
Elimination half-life (t1/2).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
|
Apparent clearance (CL/F).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
|
Apparent volume of distribution (Vz/F).
時間枠:0 hour to 8 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in plasma. |
0 hour to 8 days after dosing.
|
|
Cumulative drug excretion in urine (Ae,urine).
時間枠:0 hour to 6 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in urine. |
0 hour to 6 days after dosing.
|
|
Cumulative drug excretion fraction in urine (fe,urine).
時間枠:0 hour to 6 days after dosing.
|
Pharmacokinetic parameters of HRS-1301 in urine. |
0 hour to 6 days after dosing.
|
|
Incidence of adverse events (AEs).
時間枠:0 hour to 8 days after dosing.
|
Safety and tolerability. |
0 hour to 8 days after dosing.
|
|
Incidence of serious adverse events (SAEs).
時間枠:0 hour to 8 days after dosing.
|
Safety and tolerability. |
0 hour to 8 days after dosing.
|
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
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。