Study of Sulthiame (S-054502) in Participants With Renal Impairment and Matched Healthy Controls
A Phase 1, Multi-center, Open-label, Parallel-group Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Sulthiame (S-054502) in Participants With Varying Degrees of Renal Impairment and Matched Healthy Control Participants With Normal Renal Function
The purpose of this study is to evaluate the pharmacokinetics (PK), safety, and tolerability of sulthiame in participants with mild and moderate renal impairment compared to those in healthy participants with normal renal function.
調査の概要
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Shionogi Clinical Trials Administrator Clinical Support Help Line
- 電話番号:1-800-849-9707
- メール:Shionogiclintrials-admin@shionogi.co.jp
研究場所
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Florida
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Altamonte Springs、Florida、アメリカ、32714
- Omega Research Orlando, LLC
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Miami Lakes、Florida、アメリカ、33016
- Floridian Clinical Research
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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
Key Inclusion Criteria:
All Participants:
- Participants who are considered to be healthy (for normal renal function participants) or medically stable (for participants with renal impairment), as determined by medical evaluation including previous medical conditions/concurrent medical conditions, physical examination, clinical laboratory tests, vital sign measurements, and 12-lead electrocardiography (ECG) during the screening period and on Day -1. Participants with renal impairment should have no clinically significant changes (based on investigator clinical judgment) in previous medical conditions/concurrent medical conditions or laboratory values within 3 months prior to administration of the investigational intervention on Day 1.
- Body weight ≥ 60 kilograms (kg) for male and ≥ 50 kg for female and body mass index (BMI) within the range 18.5 to 40.0 (inclusive) kg/square meter (m^2) .
Participants With Renal Impairment (Groups A and B):
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Participants who have mild and moderate renal impairment based on estimated glomerular filtration rate (eGFR) calculated using the 2021 Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine formula and the participant's body surface area (BSA) at the screening visit (Day -28 to -2).
- Mild renal impairment: 60 to < 90 milliliters (mL)/minute (min)
- Moderate renal impairment: 30 to < 60 mL/min
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A stable medication regimen is required, defined as not starting new drug(s) or changing dosage(s) within 14 days prior to administration of the investigational intervention through the follow-up/early termination visit.
Healthy Participants With Normal Renal Function (Group C):
- Participants with clinical laboratory tests within normal reference range for the laboratory, or abnormal but considered not clinically significant by the investigator. Renal function based on eGFR, calculated based on the 2021 CKD EPI creatinine formula and the participant's BSA, must be normal (eGFR ≥ 90 mL/min) at the screening visit.
- Matched to an individual participant with moderate renal impairment (Group B) with respect to age (± 10 years), body weight (± 10 kg), and sex.
Key Exclusion Criteria:
All Participants:
- History or presence of/significant history of or current cardiovascular, respiratory, hepatic, gastrointestinal (GI), endocrinological, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the investigational intervention; or interfering with the interpretation of data.
- History of GI surgery such as gastrectomy and enterectomy that could lead to clinically significant gastrointestinal dysfunction.
- Current or chronic history of liver disease or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
- Participants with fluctuating or rapidly deteriorating renal function.
- Participation in any other clinical study or any other type of medical research involving administration of an investigational intervention (new chemical entity) within 28 days or 5 half-lives of the investigational intervention (if known) prior to dosing, whichever is longer.
Participants With Renal Impairment (Groups A and B):
- Participant with clinically significant laboratory values in the opinion of the investigator or outside the protocol-defined ranges or limits during the screening period or on Day -1.
Healthy Participants With Normal Renal Function (Group C):
- History or presence of/significant history of or current renal disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the investigational intervention; or interfering with the interpretation of data.
Note: Other protocol-defined inclusion and exclusion criteria may apply.
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:非ランダム化
- 介入モデル:並列代入
- 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 |
|---|---|
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実験的:Group A: Participants with Mild Renal Impairment
Participants with mild renal impairment will receive a single dose of sulthiame in the fasted state on Day 1. |
Tablet for oral administration
他の名前:
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実験的:Group B: Participants with Moderate Renal Impairment
Participants with moderate renal impairment will receive a single dose of sulthiame in the fasted state on Day 1. |
Tablet for oral administration
他の名前:
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実験的:Group C: Healthy Participants With Normal Renal Function
Healthy participants with normal renal function will receive a single dose of sulthiame in the fasted state on Day 1. |
Tablet for oral administration
他の名前:
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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 |
時間枠 |
|---|---|
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Maximum Observed Plasma Concentration (Cmax) of Sulthiame
時間枠:0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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|
Time to Reach Cmax (Tmax) of Sulthiame
時間枠:0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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Area Under the Plasma Concentration-time Curve Extrapolated From Time 0 to the time of the Last Quantifiable Concentration After Dosing (AUC0-last) of Sulthiame
時間枠:0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
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Cmax of Sulthiame Metabolite
時間枠:0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
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Tmax of Sulthiame Metabolite
時間枠:0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
|
|
AUC0-last of Sulthiame Metabolite
時間枠:0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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0 (predose) up to 168 hours postdose (Day 1 up to Day 8)
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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治療に及ぶ有害事象の参加者の数(TEAES)
時間枠:15日目まで1日目
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15日目まで1日目
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
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
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
- 2515A4313
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?
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
米国FDA規制機器製品の研究
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