A Study of the Effects of Hepatic Impairment on the Pharmacokinetics and Tolerability of Eliglustat Tartrate
An Open-label Pharmacokinetic and Tolerability Study of Eliglustat Tartrate Given as a Single Dose in Subjects With Mild and Moderate Hepatic Impairment, and in Matched Subjects With Normal Hepatic Function
Primary Objective:
To study the effect of mild and moderate hepatic impairment on the pharmacokinetics (PK) of eliglustat.
Secondary Objective:
To assess the tolerability of eliglustat tartrate given as a single dose in subjects with mild and moderate hepatic impairment in comparison with matched subjects with normal hepatic function.
調査の概要
詳細な説明
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
-
-
Florida
-
Miami、Florida、アメリカ、33014
- Investigational Site Number 840002
-
-
Tennessee
-
Knoxville、Tennessee、アメリカ、37920
- Investigational Site Number 840001
-
-
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 :
For subjects with hepatic impairment:
- Male or female subjects, between 18 and 79 years of age, inclusive.
- Body weight between 50.0 and 125.0 kg, inclusive if male, and between 40.0 and 110.0 kg, inclusive if female, body mass index (BMI) between 18.0 and 37 kg/m^2, inclusive.
- Stable chronic liver disease assessed by medical history, physical examination, laboratory values.
- For moderate hepatic impairment cohort: Child-Pugh total score ranging from 7 to 9, inclusive.
- For mild hepatic impairment cohort: Child-Pugh total score ranging from 5 to 6, inclusive.
For matched subjects:
- Male or female subjects, between 18 and 79 years of age, inclusive.
- Body weight within 15% of the body weight of the subjects with hepatic impairment and BMI between 18.0 and 37 kg/m^2, inclusive.
- Matched by cytochrome P450 (CYP) 2D6 predicted phenotype based on genotype.
- Certified as healthy by a comprehensive clinical assessment (detailed medical history and complete physical examination).
Exclusion criteria:
For subjects with hepatic impairment:
- Uncontrolled clinically relevant cardiovascular, pulmonary, gastrointestinal, metabolic, hematological, neurological, psychiatric, systemic, ocular, gynecologic (if female), or infectious disease, or signs of acute illness.
- Hepatocarcinoma.
- Acute hepatitis.
- Hepatic encephalopathy grade 2, 3, and 4.
- Presence or history of drug hypersensitivity, or allergic disease, including active seasonal rhinitis, diagnosed and treated by a physician.
- History or presence of drug or alcohol abuse (alcohol consumption more than 40 g per day) within 2 years before inclusion.
- If female, pregnancy (defined as positive beta-human chorionic gonadotropin [β -HCG] blood test), breastfeeding.
- P-gp inhibitors and/or inducers, CYP2D6 and/or CYP3A inhibitors and/or inducers.
- Positive result on any of the following tests: anti-human immunodeficiency virus 1 and 2 antibodies (anti-HIV1 and anti-HIV2 Ab).
- Pre-existing cardiac disease (current congestive heart failure, recent acute myocardial infarction, bradycardia, heart block, ventricular arrhythmia), long QT syndrome, or use of Class IA (eg, quinidine, procainamide) and Class III (eg, amiodarone, sotalol) anti-arrhythmic medications.
- Any subject with CYP2D6 indeterminate or ultra-rapid metabolizer (URM) phenotype.
For matched subjects:
- Any history or presence of clinically relevant cardiovascular, pulmonary, gastrointestinal, hepatic, renal, metabolic, hematological, neurological, osteomuscular, articular, psychiatric, systemic, ocular, gynecologic (if female), or infectious disease, or signs of acute illness.
- Presence or history of drug hypersensitivity, or allergic disease diagnosed and treated by a physician.
- If female, pregnancy (defined as positive β-HCG blood test), breastfeeding.
- For subjects 50 years of age and younger: any medication (including St John's Wort) within 14 days before inclusion, or within 5 times the elimination half-life or pharmacodynamic half-life of that medication, whichever the longest, with the exception of hormonal contraception or menopausal hormone replacement therapy, any vaccination within the last 28 days, and any biologics (antibody or its derivatives) given within 4 months before inclusion.
- For subjects older than 50 years of age: any significant change in chronic treatment medication within 14 days before inclusion.
- P-gp inhibitors and/or inducers, CYP2D6 and/or CYP3A inhibitors and/or inducers.
- Positive result on any of the following tests: hepatitis B surface antigen (HBs Ag), anti-hepatitis C virus (anti-HCV) antibodies, anti-HIV1 and anti-HIV2 Ab.
- History or presence of drug or alcohol abuse (alcohol consumption more than 40 g per day) within 2 years before inclusion.
- Pre-existing cardiac disease (current congestive heart failure, recent acute myocardial infarction, bradycardia, heart block, ventricular arrhythmia), long QT syndrome, or use of Class IA (eg, quinidine, procainamide) and Class III (eg, amiodarone, sotalol) anti-arrhythmic medications.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
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 |
|---|---|
|
実験的:GZ385660 (健康な被験者)
エリグルスタット酒石酸塩の単回投与は、摂食条件下で投与されます。
|
剤形: カプセル 投与経路: 経口
他の名前:
|
|
実験的:GZ385660 (subjects with mild hepatic impairment)
Single dose of eliglustat tartrate will be given under fed conditions
|
剤形: カプセル 投与経路: 経口
他の名前:
|
|
実験的:GZ385660 (subjects with moderate hepatic impairment)
Single dose of eliglustat tartrate will be given under fed conditions
|
剤形: カプセル 投与経路: 経口
他の名前:
|
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 |
|---|---|
|
Assessment of PK parameter: Maximum plasma concentration observed (Cmax)
時間枠:3 days
|
3 days
|
|
Assessment of PK parameter: Area under the plasma concentration (AUC)
時間枠:3 days
|
3 days
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
PK パラメーターの評価: 血漿濃度対時間曲線の下の面積 (AUClast)
時間枠:3日
|
3日
|
|
PK パラメーターの評価: 見かけの全身クリアランス (CL/F)
時間枠:3日
|
3日
|
|
PK パラメーターの評価: 終末期の見かけの分布量 (Vz/F)
時間枠:3日
|
3日
|
|
PKパラメータの評価:予測蓄積率(Rac、pred)
時間枠:3日
|
3日
|
|
PKパラメータの評価:終末半減期(t1/2z)
時間枠:3日
|
3日
|
|
有害事象の数
時間枠:最大10日間
|
最大10日間
|
|
Change from baseline in ECG parameter
時間枠:Baseline, Up to 10 days
|
Baseline, Up to 10 days
|
協力者と研究者
研究記録日
主要日程の研究
研究開始
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 (見積もり)
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
- POP13777
- U1111-1170-3678 (その他の識別子:UTN)
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。