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A Study to Assess Safety, Tolerability and Exposure of 4ET1103 in Healthy Human Volunteers

3 settembre 2026 aggiornato da: 4E Therapeutics

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

This study will dose healthy human volunteers with either active drug (4ET1103) or placebo. Each study subject will receive a single dose of either active drug or placebo, and will then be monitored for safety, tolerability and exposure of active drug.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

This is a randomized, double-blind, placebo-controlled SAD study conducted in approximately 40 healthy male and female volunteers. The study drug (4ET1103 or placebo) will be administered orally under fasting condition. 40 subjects (8 subjects/cohort) will participate across 5 dose cohorts (45, 135, 270, 450 and 720 mg) of 4ET1103.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

40

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Texas
      • Austin, Texas, Stati Uniti, 78744
        • PPD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Sì

Descrizione

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:

    1. 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).
    2. 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)
    3. 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.
    4. 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.
    5. 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:

  1. 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.
  2. 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
  3. 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
  4. 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).
  5. 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.
  6. 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.
  7. History of organ transplant, including history of bone marrow transplant.
  8. 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.
  9. 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.
  10. Subjects who have received any vaccines within 30 days prior to Day 1
  11. Donated or lost blood >500 ml within 60 days prior to Screening
  12. 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.
  13. 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.
  14. Positive serologic findings for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody (Ab), and/or Human immunodeficiency virus (HIV) Ab at Screening.
  15. Positive Columbia-Suicide Severity Rating Scale (C-SSRS) at Screening
  16. Surgery within the past 90 days prior to Day 1 as determined by the Investigator to be clinically relevant.
  17. 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.

  18. 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.
  19. 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:

    1. Mild first-degree A-V block (P-R interval <0.23 sec)
    2. Right or left axis deviation
    3. Incomplete right bundle branch block
    4. Isolated left anterior fascicular block (left anterior hemiblock)
  20. 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.
  21. Subject with abnormal liver function test (LFT) at Screening or Day -1.
  22. 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.
  23. Receipt of an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to dosing on Day 1.
  24. 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.
  25. Subjects with hypersensitivity to any excipients present in study drug (excipients listed in Investigator's Brochure).

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Cohort 1 active
45 mg active
MNK inhibitor for treatment of neuropathic pain
Altri nomi:
  • 4ET1103
Comparatore placebo: Cohort 2 placebo
placebo for 135 mg
Placebo for MNK inhibitor
Comparatore placebo: Cohort 3 placebo
placebo for 270 mg
Placebo for MNK inhibitor
Comparatore placebo: Cohort 4 placebo
placebo for 450 mg
Placebo for MNK inhibitor
Comparatore placebo: cohort 5 placebo
placebo for 720 mg
Placebo for MNK inhibitor
Comparatore placebo: Cohort 1 placebo
Placebo for 45 mg
Placebo for MNK inhibitor
Sperimentale: Cohort 2 active
135 mg active
MNK inhibitor for treatment of neuropathic pain
Altri nomi:
  • 4ET1103
Sperimentale: Cohort 3 active
270 mg active
MNK inhibitor for treatment of neuropathic pain
Altri nomi:
  • 4ET1103
Sperimentale: Cohort 4 active
450 mg active
MNK inhibitor for treatment of neuropathic pain
Altri nomi:
  • 4ET1103
Sperimentale: Cohort 5 active
720 mg active
MNK inhibitor for treatment of neuropathic pain
Altri nomi:
  • 4ET1103

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change from baseline in hematology parameters
Lasso di tempo: 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
Lasso di tempo: 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.
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Drug excreted in urine (Ae) to be determined.
Lasso di tempo: 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)
Lasso di tempo: 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.
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
The change from baseline in the levels of p-eIF4E will be assessed in whole blood at specified timepoints
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Investigatori

  • Investigatore principale: Kristie Miller, MD, PPD Development, LP

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

18 aprile 2025

Completamento primario (Effettivo)

18 agosto 2025

Completamento dello studio (Effettivo)

18 agosto 2025

Date di iscrizione allo studio

Primo inviato

22 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

8 maggio 2026

Primo Inserito (Effettivo)

14 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

8 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 4ET1103-001
  • U44NS115692 (Sovvenzione/contratto NIH degli Stati Uniti)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Individual participant data will not be shared. Data contain proprietary information about an investigational new drug and cannot be disclosed prior to regulatory approval. Patient confidentiality also prohibits sharing due to detailed clinical and pharmacokinetic data from a small cohort.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .