A Single and Multiple Dose Study to Evaluate the Safety and Effects of Inhaled ICF001 Dry Powder in Healthy Participants
2026年8月31日 更新者:VIVID CLINICAL SERVICES PTY LTD
A Randomized, Double-Blind, Placebo-Controlled Phase 1 Clinical Trial to Evaluate the Safety, Tolerability, and Pharmacokinetic Characteristics of Single and Multiple Inhaled Doses of ICF001 Dry Powder in Healthy Adult Participants
The primary purpose of this study is to evaluate the safety, tolerability and pharmacokinetic characteristics of ICF001 following inhaled administration of single and multiple ascending doses in healthy participants.
調査の概要
詳細な説明
This study will consist of 2 parts: a single ascending dose (SAD) study and a multiple ascending dose (MAD) study in healthy participants.
研究の種類
介入
入学 (推定)
72
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
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Queensland
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Brisbane、Queensland、オーストラリア、4006
- Q-Pharm Pty Ltd
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コンタクト:
- Michael Wong, Dr, MD, MPhil, BMedSci
- 電話番号:0737072720
- メール:m.wong@nucleusnetwork.com.au
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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:
- Understand the study procedures and methods, voluntarily participate in this study, and provide written informed consent.
- Healthy adult participants aged 18 to 55 years (inclusive), both genders.
- Body Mass Index (BMI) equal to (=) weight/height squared kilogram per meter square (kg/m^2)): 18 less than or equal to (<=) BMI <=32; male weight greater than or equal to (>=) 50.0 kilogram (kg) and less than (<) 100.0 kg, female weight >=45.0 kg and <100.0 kg.
- Confirmed to have no clinically significant abnormalities through physical examination, laboratory tests, vital signs assessment, and electrocardiogram (ECG), and determined by the investigator to be medically healthy.
- Participants whose peak inspiratory flow rate measured by In-Check^TM DIAL G16 is between 30 to 60 liters per minute (L/min) and whose total inspiratory duration exceeds 2 seconds.
- Participants must be able to correctly and effectively use the inhaler device during the screening period and throughout the study.
- Sexually active female participants of childbearing potential must agree to use effective contraception from screening until 35 days after the last dose and must not become pregnant or donate eggs during this period; Sexually active male participants with partners of childbearing potential must agree to use effective contraception from the first dose until 95 days after the last dose and must not donate sperm during this time; their fertile male or female partners must also agree to use effective contraception during this period.
- Ability to successfully complete test dosing procedure following inhalation training on Day-1.
- Able to understand the study procedures and provide signed informed consent to participate in the study.
Exclusion Criteria:
- Participants with a history of any clinically significant disease (including both past and current medical conditions), including but not limited to respiratory, cardiovascular, neurological, gastrointestinal, hematologic, endocrine, immune, dermatologic, malignancy, neuropsychiatric, ophthalmologic, or metabolic disorders, or any other condition that, in the opinion of the investigator (or designee), would make the participant unsuitable for participation in the study. A history of bariatric surgery or prior cholecystectomy; a history of eczema (provided no use of topical or systemic steroid treatments within 3 months prior to screening); a history of gestational diabetes that has fully resolved; current or past attention deficit hyperactivity disorder (ADHD), anxiety, or depression (provided no use of antidepressant medication within 6 months prior to screening); and Gilbert's syndrome are not considered exclusionary, provided they are not currently clinically significant and are acceptable at the investigator's discretion.
- Participants who have undergone any major surgery within 3 months, or any minor surgery within 1 months prior to dosing, or who plan to undergo surgery during the study, or who have undergone surgery that may significantly affect the pharmacokinetic (PK) or safety evaluation of the study drug.
- Participants with clinically significant oral diseases that, in the investigator's judgment, may affect the study (e.g., oral candidiasis, oral ulcers, lesions of the oral mucosa, etc.).
- Participants with clinically significant nasal diseases such as severe rhinitis, sinusitis, nose cavity and nose septum infections and lesions.
- Risk of bleeding: History of bleeding disorders, active peptic ulcer, or history of gastrointestinal bleeding; abnormal platelet count, international normalized ratio (INR), or activated partial thromboplastin Time (APTT) during the screening period.
- History of asthma, chronic obstructive pulmonary disease (COPD), or reactive airway disease, or pulmonary function test findings consistent with asthma or COPD.
- History of orthostatic hypotension, unexplained syncope, or hypertension.
- During screening or re-screening, participants with a systolic blood pressure of <90 millimeters of mercury (mmHg) or a diastolic blood pressure of <50 mmHg after sitting for 5 minutes.
- During screening or re-screening, participants with a systolic blood pressure of greater than (>) 140 mmHg or a diastolic blood pressure of >90 mmHg after sitting for 5 minutes.
- During screening or re-screening, participants with a heart rate of >100 beats/minute after sitting for 5 minutes.
- Participants with a fever (temperature >37.5 degrees Celsius [°C]) or symptomatic respiratory infection within 1 month prior to dosing, or those with any infection requiring systemic antibiotics/antiviral medications within 3 months prior to screening, or those with a history of recurrent infections.
- Positive for Human Immunodeficiency Virus (HIV), hepatitis B surface antigen, and hepatitis C.
- During screening/baseline visit, participants with alanine transaminase (ALT), aspartate transaminase (AST), gamma-glutamyl transferase (GGT), or total bilirubin >=1.5 the upper limit of normal (ULN).
- Screening/Baseline Visit: Forced Expiratory Volume in 1 Second (FEV1) and Forced Vital Capacity (FVC) <80 percentage (%) of predicted value, or FEV1/FVC < 0.7, or an oxygen saturation (SpO₂) <95%. Spirometry may be repeated at the same visit for a total of 3 tests if initial results are considered unacceptable due to poor effort or technical issues, with the best value recorded.
- Participants who smoked (including vaping) within 3 months prior to dosing, or with positive cotinine test results.
- Participants with potential risk of airway hyperreactivity, such as those with prolonged exposure to dust or harmful gases.
- Participants with a history of heavy alcohol consumption within 3 months prior to screening, defined as >14 alcohol units per week for males and >10 alcohol units per week for females (where 1 standard unit =375 milliliter (mL) of mid-strength beer (3.5% alcohol/volume), 100 mL of wine (13.5% alcohol/volume), or 30 mL of spirits (40% alcohol/volume)), or with a positive breath alcohol test, or who are unable to abstain from alcohol during the study period.
- Participants who have received any known moderate or strong inhibitors/inducers of cytochrome P450 (CYP) enzymes (for example; barbiturates, phenothiazines, cimetidine, carbamazepine) within the 30 days prior to the study, and for whom the investigator believes that these medications may affect the participant's safety or the validity of the study results.
- Participants with a history of drug abuse within 3 months prior to screening, or those with a positive urine drug screen.
- Participants who have participated in any clinical trials of drugs or medical devices within 5 half-lives or 3 months after the last dose/administration, whichever is longer, prior to screening.
- Participants who have donated or lost >=400 mL of blood within 30 days prior to dosing.
- Participants with difficulty in intravenous blood collection or intolerance to venipuncture, or those with a history of vasovagal syncope.
- Participants who have used any medication (including prescription drugs, over-the-counter drugs, vitamin supplements, or traditional medicines, especially anticoagulants, antiplatelet agents, non-steroidal anti-inflammatory drugs, vasodilators, or potent CYP2C8 inhibitors such as gemfibrozil and rifampin) or received any health supplements or vaccines within 7 days prior to dosing (or 5 half-lives of the drug, whichever is longer).
- Participants who have consumed foods that may affect drug metabolism within 7 days prior to dosing (including grapefruit or grapefruit products, pitaya, mango, pomelo, etc.), or those with other dietary habits that the investigator believes may affect the absorption, distribution, metabolism, or excretion of the drug, or those who are unwilling to discontinue consuming the aforementioned foods during the study period.
- Participants who have consumed any coffee or tea, as well as beverages and foods containing coffee or tea ingredients, within 48 hours prior to dosing, or those who are unwilling to discontinue consuming these foods during confinement, and within 24 hours before each follow-up visit.
- Participants with special dietary requirements who cannot comply with a standard diet.
- Participants with a known allergy to the study drug or any of its components.
- Female participants who are pregnant or breastfeeding, or who have plans to become pregnant during the study period or within 2 months after the last dose.
- Participants are deemed by the investigator to be unsuitable for participation in the 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:処理
- 割り当て:ランダム化
- 介入モデル:順次割り当て
- マスキング:4倍
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:Part 1- SAD: ICF001
Participants will receive a single inhaled dose of ICF001 or placebo at 5 escalating dose levels from Day 1 to 3, under fasting conditions.
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ICF001 capsule-based inhalation powders.
Matching-placebo capsule-based inhalation powders.
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実験的:Part 2- MAD: ICF001
Participants will receive a multiple inhaled doses of ICF001 or placebo at 4 escalating dose levels from Days 1 to 7, under fasting conditions.
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ICF001 capsule-based inhalation powders.
Matching-placebo capsule-based inhalation powders.
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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 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Number of Participants With an Adverse Event (AE)
時間枠:From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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An AE is any untoward medical occurrence in a clinical study participant, temporarily associated with the use of study intervention, whether or not considered related to the study intervention.
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From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Number of Participants With Clinically Significant Change From Baseline in Local Tolerability Findings
時間枠:From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Local tolerability includes observation of cough, wheezing, chest tightness, sore throat, choking cough, throat itching, and foreign object sensation in the throat.
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From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Number of Participants With Clinically Significant Change From Baseline in Clinical Laboratory Findings
時間枠:From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Laboratory parameters included hematology, blood chemistry, urinalysis, coagulation tests.
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From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Number of Participants With Clinically Significant Change From Baseline in Electrocardiogram (ECG) Findings
時間枠:From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Number of Participants With Clinically Significant Change From Baseline in Pulmonary Function Test Abnormalities
時間枠:From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Number of Participants With Clinically Significant Change From Baseline in Vital Sign Values
時間枠:From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Vital signs included blood pressure, heart rate, respiratory rate, and body temperature.
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From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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Number of Participants With Clinically Significant Change From Baseline in Physical Examination Findings
時間枠:From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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From start of the study up to follow up (up to 38 days [SAD] and 50 Days [MAD])
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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SAD and MAD: Maximum Observed Plasma Concentration (Cmax) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
|
SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD and MAD: Time of the Maximum Measured Plasma Concentration (Tmax) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD and MAD: Area Under the Plasma Concentration-Time Curve from Zero to the Last Measurable Time Point (AUC0-t) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
|
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SAD and MAD: Area Under the Plasma Concentration-Time Curve from Zero to Infinity (AUC0-∞) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD and MAD: Terminal Elimination Half-life (t½) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD and MAD: Terminal Elimination Rate Constant (λz) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD: Predose, 5,15,30 mins,1,1.5,2,4,6,8,10,12,24,36,48 hrs postdose; MAD: Day 1: predose, 5,15,30 mins,1,1.5, 2,4,6,8,10,12 hrs post first dose; Days 2-7: predose; Day 7: 5,15,30 mins,1,1.5, 2,4,6,8,10,12,24 hours (Day 8) and 48 hours (Day 9) postdose
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SAD: Apparent Clearance (CL/F) of ICF001 Only
時間枠:Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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SAD: Apparent Volume of Distribution (Vd/F) of ICF001 Only
時間枠:Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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SAD: Mean Residence Time (MRT) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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SAD: Area Under the Curve Extrapolated Percentage (AUC_%Extrap) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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Predose, 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24, 36, 48 hours postdose
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MAD: Area Under the Concentration-Time Curve from Zero to 12 Hours (AUC0-12) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Area Under the Plasma Concentration-Time Curve from Zero to the Last Measurable Time Point (AUC0-t) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Steady-state Average Concentration (Cavg,ss) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Maximum Plasma Concentration in Steady State (Cmax,ss) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Steady-state Trough Plasma Concentration (Ctrough,ss) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Time of the Maximum Measured Plasma Concentration Steady State (Tmax,ss) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Area Under the Plasma Concentration-Time Curve Over the Dosing Interval at Steady State (AUC0-τ, ss) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Apparent Clearance at Steady State (CLss/F) of ICF001 Only
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Apparent Volume of Distribution at Steady State (Vdss/F) of ICF001 Only
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Accumulation Ratio (Rac) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Degree of Fluctuation (DF) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Steady-State Plasma Concentration Fluctuation (Swing) of ICF001 and its Active Metabolite IC001-R1
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Ratio of Maximum Plasma Concentration (RCmax) of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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MAD: Ratio of Area Under the Plasma Concentration-Time Curve (RAUC) Following the last Dose of ICF001 and its Active Metabolite (IC001-R1)
時間枠:Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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Day 1: predose, 5, 15, 30 mins,1,1.5, 2, 4, 6, 8, 10,12 hrs post first dose; Days 2-7: predose; Day 7: 5, 15, 30 mins,1, 1.5, 2, 4, 6, 8, 10, 12, 24 hours (Day 8) and 48 hours (Day 9) postdose
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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。
捜査官
- スタディディレクター:Jian Wang、VIVID CLINICAL SERVICES PTY LTD
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 (推定)
2026年9月1日
一次修了 (推定)
2027年5月14日
研究の完了 (推定)
2027年8月26日
試験登録日
最初に提出
2026年8月31日
QC基準を満たした最初の提出物
2026年8月31日
最初の投稿 (実際)
2026年9月4日
学習記録の更新
投稿された最後の更新 (実際)
2026年9月4日
QC基準を満たした最後の更新が送信されました
2026年8月31日
最終確認日
2026年7月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- nIC001-202601
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。