A Study to Assess Safety, Tolerability and Exposure of 4ET1103 in Healthy Human Volunteers
A First in Human Randomized, Double-Blind, Placebo Controlled Single Ascending Dose (SAD) Phase 1 Study to Determine Safety, Tolerability, and Pharmacokinetics of 4ET1103 in Healthy Volunteers
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
-
-
Texas
-
Austin、Texas、アメリカ、78744
- PPD
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Healthy males and females (sex at birth) between 18 and 65 years of age; inclusive based on the date of Screening.
- Body mass index (BMI) between 18 and 32 kg/m2 (inclusive) and weigh at least 50 kg at Screening and Day -1.
- Provision of signed and dated, written informed consent prior to any study-specific procedures
- Female subjects have a negative serum pregnancy test result at Screening and negative urine pregnancy test result at Day -1.
Female subjects with male partners must meet one of the following criteria:
- Using a medically acceptable form of birth control for at least 30 days prior to Screening (60 days on oral contraceptives) until 3 months following the last dose of study drug [e.g., hormonal contraceptives (oral, patch, injectable or vaginal ring), implantable device (implantable rod or intrauterine device), bilateral tubal ligation/tubal occlusion or a double barrier (e.g., diaphragm, cervical cap, condom in conjunction with spermicide or sponge)]. For female subjects using hormonal contraceptives, it is also required to use at least one additional form of contraception, i.e., implantable device (implantable rod or intrauterine device), or a double barrier method (e.g., diaphragm, cervical cap, or condom in conjunction with spermicide or sponge).
Surgically sterile for at least 3 months prior to Screening by one of the following means:
- Bilateral salpingectomy (with or without oophorectomy)
- Surgical hysterectomy
- Bilateral oophorectomy (with or without hysterectomy)
Postmenopausal, defined as the following:
- Female subjects with 12 months consecutive amenorrhea and follicle-stimulating hormone (FSH) levels greater than 40 international units per liter (IU/L) at Screening.
- Female subjects of reproductive potential who are abstinent of heterosexual activity (when in line with the preferred and usual lifestyle of the subject), are acceptable provided they agree to a double barrier method for at least 3 months after their last dose of the study drug should they become sexually active with a male partner.
- Females must agree to avoid egg donation throughout the study and for at least 3 months after last dose of study drug.
- Male subjects with female partners have history of vasectomy or must agree to utilize a highly effective method of contraception (condom with spermicide) during heterosexual intercourse from clinic admission until at least 3 months following the last dose of the study drug and must refrain from donating sperm for this same period.
- Considered healthy by the Investigator, based on subject's reported medical history, full physical examination, clinical laboratory tests, 12-lead ECG, and vital signs at Screening and Day -1.
- Willing and able to adhere to study restrictions and to be confined at the clinical research center
- Subjects willing to defer receiving any vaccines (e.g. influenza or coronavirus or pneumococcal vaccines) within 30 days prior to the first dose of study drug (Day 1) and throughout the study.
- Nicotine-free (cigarettes, pipe, cigar, chewing tobacco, nicotine patches, vapes, etc.) for at least 3 months before Screening and a negative urine cotinine test at Screening and Day -1.
Exclusion Criteria:
- History or presence of any illness, condition, or finding that in the opinion of the Principal Investigator (PI) or designee would put the subject or study conduct at risk, or have the potential to confound the results of the study, if the subject were to participate in the study.
- History or presence of significant cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatologic, neurological, bleeding disorder or psychiatric disease or drug hypersensitivity as determined by the Investigator
- Any surgical or medical condition that could interfere with the absorption, distribution, metabolism, or excretion of the drug. Cholecystectomies will be exclusionary and uncomplicated appendectomies will not be exclusionary
- In opinion of the Investigator, the subject has history of any true drug allergy; excluding histories limited to mild to moderate gastrointestinal distress (nausea, anorexia, diarrhea, infrequent vomiting).
- History of alcohol abuse (drinking 14 units of alcohol per week: 1 unit = 360 mL of beer, or 37 mL of spirits, or 120 mL of wine) within 3 months prior to Screening, or positive urine alcohol test at Screening or Day -1. Subjects must agree to abstain from alcohol intake from 72 hours before study drug administration through discharge from the CRU.
- History of prescription drug abuse, or marijuana or cannabis product use or illicit drug use within 6 months prior to Screening, or positive findings on the urine drug screen at Screening or Day -1.
- History of organ transplant, including history of bone marrow transplant.
- Use of any prescription (excluding contraceptives) medication, over the counter (OTC) medication or herbal supplements within 7 days or 5 half-lives, whichever is longer prior to Day 1.
- Evidence of severe acute respiratory syndrome-related coronavirus-2 (SARS-CoV-2) infection or oral temperature >38°C at Day -1. During the study, if subjects have infections, the subjects may continue the study at the discretion of the Investigator. In the case of COVID-19 infection, subject will be withdrawn.
- Subjects who have received any vaccines within 30 days prior to Day 1
- Donated or lost blood >500 ml within 60 days prior to Screening
- Acute illness within 14 days of study Day 1; acute illness occurring before this must show complete recovery at least 14 days prior to Day 1.
- Regular consumption of > 3caffeine - or xanthine-containing products in 2 weeks before Screening and unwilling to consume <3 caffeine - or xanthine-containing products while confined at the CRU.
- Positive serologic findings for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody (Ab), and/or Human immunodeficiency virus (HIV) Ab at Screening.
- Positive Columbia-Suicide Severity Rating Scale (C-SSRS) at Screening
- Surgery within the past 90 days prior to Day 1 as determined by the Investigator to be clinically relevant.
Seated systolic blood pressure (SBP) not within the range of 90 mmHg to 140 mmHg and diastolic blood pressure (DBP) not within the range of 50 mmHg to 90 mmHg at Screening or Day 1.
Note: If a subject fails to meet SBP and/or DBP criteria, optional repeat visits/measurements can, at the discretion of the Investigator, to be completed. For those subjects who have a repeat blood pressure measurement, the repeat value will be used to determine eligibility.
- Heart rate <40 bpm or >99 bpm at Screening or Day -1. Note: If a subject fails to meet heart rate criteria, optional repeat visits/measurements can, at the discretion of the Investigator, to be completed. For those subjects who have a repeat blood pressure measurement, the repeat value will be used to determine eligibility.
Any clinically significant ECG abnormality at Screening (as deemed by the Investigator).
NOTE: The following (a-d) are considered not clinically significant without consulting Sponsor's Medical Monitor:
- Mild first-degree A-V block (P-R interval <0.23 sec)
- Right or left axis deviation
- Incomplete right bundle branch block
- Isolated left anterior fascicular block (left anterior hemiblock)
- QTcF interval >450 msec for male and >470 msec for female (the average value for the triplicate ECG at Screening and Day -1), or history of prolonged QT syndrome.
- Subject with abnormal liver function test (LFT) at Screening or Day -1.
- Subjects with estimated glomerular filtration rate (eGFR) < or = 75 mL/min/1.73m2 using Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation 2021 at Screening or Day -1.
- Receipt of an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to dosing on Day 1.
- Subjects who have taken a special diet (including dragon fruit, mango, grapefruit or grapefruit juice and other known inhibitors of CYP) or strenuous exercise, or other factors affecting drug absorption, distribution, metabolism, and excretion within 5 days before Day 1.
- Subjects with hypersensitivity to any excipients present in study drug (excipients listed in Investigator's Brochure).
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:並列代入
- 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 |
|---|---|
|
実験的:Cohort 1 active
45 mg active
|
MNK inhibitor for treatment of neuropathic pain
他の名前:
|
|
プラセボコンパレーター:Cohort 2 placebo
placebo for 135 mg
|
Placebo for MNK inhibitor
|
|
プラセボコンパレーター:Cohort 3 placebo
placebo for 270 mg
|
Placebo for MNK inhibitor
|
|
プラセボコンパレーター:Cohort 4 placebo
placebo for 450 mg
|
Placebo for MNK inhibitor
|
|
プラセボコンパレーター:cohort 5 placebo
placebo for 720 mg
|
Placebo for MNK inhibitor
|
|
プラセボコンパレーター:Cohort 1 placebo
Placebo for 45 mg
|
Placebo for MNK inhibitor
|
|
実験的:Cohort 2 active
135 mg active
|
MNK inhibitor for treatment of neuropathic pain
他の名前:
|
|
実験的:Cohort 3 active
270 mg active
|
MNK inhibitor for treatment of neuropathic pain
他の名前:
|
|
実験的:Cohort 4 active
450 mg active
|
MNK inhibitor for treatment of neuropathic pain
他の名前:
|
|
実験的:Cohort 5 active
720 mg active
|
MNK inhibitor for treatment of neuropathic pain
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change from baseline in hematology parameters
時間枠:14 days
|
Hematology laboratory parameters (for example, complete blood count including erythrocytes, leukocytes with differential, hemoglobin, hematocrit, and platelets) will be summarized as observed values and changes from baseline at each postdose time point, and the number of subjects with clinically significant abnormalities will be reported.
|
14 days
|
|
Change from baseline in serum chemistry parameters
時間枠:14 days
|
Serum chemistry laboratory parameters (for example, electrolytes, liver function tests, renal function tests, and lipids) will be summarized as observed values and changes from baseline at each post dose time point, and the number of subjects with clinically significant abnormalities will be reported.
|
14 days
|
|
Change from baseline in urinalysis parameters.
時間枠:14 days
|
Urinalysis parameters (for example, urine specific gravity, pH, protein, glucose, ketones, blood/occult blood, nitrite, leukocyte esterase, and bilirubin) will be summarized as observed values and changes from baseline at each post dose time point, and the number of subjects with clinically significant abnormalities will be reported
|
14 days
|
|
Change from baseline in coagulation parameters
時間枠:14 days
|
Coagulation parameters (for example, prothrombin time, international normalized ratio, and activated partial thromboplastin time) will be summarized as observed values and changes from baseline at each post dose time point, and the number of subjects with clinically significant abnormalities will be reported.
|
14 days
|
|
Change from bassline in vital signs
時間枠:14 days
|
Vital signs, including systolic and diastolic blood pressure, pulse rate, respiratory rate, and body temperature, will be summarized as observed values and changes from baseline at each postdose time point, and the number of subjects with clinically significant abnormalities will be reported.
|
14 days
|
|
Change from baseline in 12-lead ECG parameters
時間枠:14 days
|
Twelve-lead ECG parameters (for example, heart rate, PR interval, QRS duration, QT interval, and QTc) will be summarized as observed values and changes from baseline at each post dose time point, and the number of subjects with clinically significant ECG abnormalities will be reported.
|
14 days
|
|
Incidence of treatment-emergent adverse events (TEAEs)
時間枠:72 hours
|
The number of subjects with treatment-emergent adverse events (TEAEs), including serious and non-serious AEs, will be summarized by system organ class and preferred term, severity, and relationship to study drug from first dose through the end of safety follow-up
|
72 hours
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Drug excreted in urine (Ae) to be determined.
時間枠:24 hours after single dose 4ET1103
|
The amount of drug excreted in urine will be calculated in milligrams
|
24 hours after single dose 4ET1103
|
|
Peak Plasma Concentration (Cmax)
時間枠:PK measurements will be followed for out to 7 days from single dose of 4ET1103
|
Peak Plasma Concentration (Cmax) will be measured and reported in ng/mL.
|
PK measurements will be followed for out to 7 days from single dose of 4ET1103
|
|
Renal clearance (CLR) will be measured.
時間枠:24 hours following single dose of 4ET1103
|
Renal clearance (CLR) will be presented in liters/hour (L/h)
|
24 hours following single dose of 4ET1103
|
|
Fraction of dose excreted renally (Fe)
時間枠:24 hours following single dose of 4ET1103
|
The fraction of dose excreted renally will be measured following oral single ascending dose administration
|
24 hours following single dose of 4ET1103
|
|
Area under the plasma concentration versus time curve (AUC)
時間枠:PK measurements out to 7 days following single dose of 4ET1103
|
Area under the plasma concentration versus time curve (AUC) will be measured and reported (h x ng/mL)
|
PK measurements out to 7 days following single dose of 4ET1103
|
|
Time to maximum concentration (Tmax)
時間枠:Monitoring up to 7 days following single dose of 4ET1103
|
Tmax will be determined and reported in hours (h)
|
Monitoring up to 7 days following single dose of 4ET1103
|
|
Half life (T1/2) will be determined
時間枠:Monitoring for up to 7 days following single dose of 4ET1103
|
Half life (T1/2) will be determined and reported in hours (h)
|
Monitoring for up to 7 days following single dose of 4ET1103
|
|
Apparent total body clearance (CL/F)
時間枠:Up to 7 days following single dose of 4ET1103
|
Apparent total body clearance (CL/F) will be determined and reported as liters/hour (L/h)
|
Up to 7 days following single dose of 4ET1103
|
|
Apparent volume of distribution (Vz/F)
時間枠:Up to 7 days following single dose of 4ET1103
|
Vz/F will be determined and reported in liters (L)
|
Up to 7 days following single dose of 4ET1103
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The change from baseline in the levels of p-eIF4E will be assessed in whole blood at specified timepoints
時間枠:Out to 7 days post dose 4ET1103
|
In whole blood samples, levels of p-eIF4E will be determined and reported as the change from baseline (prepose levels of p-eIF4E versus postdose levels of p-eIF4E)
|
Out to 7 days post dose 4ET1103
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Kristie Miller, MD、PPD Development, LP
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
本研究に関する用語
その他の研究ID番号
- 4ET1103-001
- U44NS115692 (米国 NIH グラント/契約)
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?
IPD プランの説明
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
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。