Ta strona została przetłumaczona automatycznie i dokładność tłumaczenia nie jest gwarantowana. Proszę odnieść się do angielska wersja za tekst źródłowy.

Phase 1 Study on the Safety, Tolerability, and Pharmacokinetics of JST-018 in Healthy Adults

14 maja 2026 zaktualizowane przez: Just-Evotec Biologics

Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of JST-018 in Healthy Adults

The goal of this clinical trial is to learn if a single dose of the study drug, JST-018, is safe and tolerable when administered by injection into the arm or thigh muscle of healthy men and women aged 18 to 55. The main questions it aims to answer are:

  • Is a single administration of JST-018 safe?
  • What is the concentration of the JST-018 in the blood over time?
  • Do antibodies to JST-018 develop following a dose of JST-018? Researchers will compare JST-018 to Placebo to see if there are any differences in the safety and tolerability of a single dose at different dose levels.

Participants will be confined to the clinic for the first 3 days. They will receive an injection on the second day, and then return for 9 more visits over the period of 1 year for:

  • Physical exam with vital signs
  • Electro-cardiogram (ECG)
  • Bood collection for clinical labs and research samples
  • Urine sample
  • Assessment of potential adverse effects and medications taken

Przegląd badań

Szczegółowy opis

This is a Phase 1, first-in-human (FIH), randomized, double-blind, placebo-controlled, single ascending dose (SAD) study to assess the safety, tolerability, and PK of a single dose of JST-018 administered IM to healthy participants.

The study will be comprised of a minimum of 3 cohorts (Cohorts A, B, and C, with 12 participants per cohort), each evaluating a single dose of JST-018 administered IM. In each cohort, 2 sentinel participants will be randomized 1:1 such that one participant receives JST-018 and 1 participant receives placebo. Following a favorable blinded safety review committee (SRC) review of sentinel safety data collected through Day 8, the remainder of the cohort (10 non-sentinel participants) will be randomized 4:1 to JST-018 or placebo, and will be dosed.

All safety data for all participants in the current cohort through Day 8 will be reviewed by the SRC in a blinded fashion for each dose cohort before escalating to the next dose cohort (for escalation from Cohort A to Cohort B and escalation from Cohort B to Cohort C); A recommendation on whether to implement Cohort D (along with a recommended dose of JST-018 to be evaluated in Cohort D) may be provided by the SRC following review of blinded safety data from Cohorts A, B, and C.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

48

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • Nevada
      • Las Vegas, Nevada, Stany Zjednoczone, 89113
        • PPD Las Vegas Clinical Research Unit
        • Kontakt:
          • Numer telefonu: (877) 362-2608

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Tak

Opis

Inclusion Criteria:

  1. Healthy men or women 18 to 55 years of age
  2. BMI between 18 and 32 kg/m2
  3. Negative serum pregnancy test
  4. Use of highly effective birth control method(s) for a minimum of 60 days prior to consent and is willing to continue use for at least 12 months, or abstinence
  5. In good general health as determined by medical history, exams and tests

Exclusion Criteria:

  1. Acute illness or fever (≥100.4°F) within 7 days prior to dosing
  2. Any history of receiving treatment, vaccine, or monoclonal antibodies (mAbs) against smallpox, monkeypox, or other orthopox viruses.
  3. Receipt of any vaccine within 30 days prior to Screening, planned receipt of any vaccine prior to Day 1, or planned receipt of any vaccines before 45 days post-injection.
  4. Any medical condition for which IM injections would be contraindicated in the opinion of the investigator (eg, bleeding disorders, anticoagulant therapy, and severe thrombocytopenia)
  5. History of congenital or acquired immunodeficiency syndrome, , including positive human immunodeficiency virus (HIV-1/-2) antibody result
  6. Prior solid organ or bone marrow transplant
  7. Clinically significant corneal or lens abnormality as determined by history, clinical examination, or diagnostic imaging. Including, but not limited to:

    • Corrected vision of less (worse) than 20/40
    • History of any clinically significant history of eye trauma, in the opinion of the investigator
    • History of cataracts or current cataracts
    • Lens opacity greater than NC2, C2, or P0 as determined by the Lens Opacities Classification System (LOCS) III
    • History of uveitis (including acute)
    • Use of ocular or inhaled prescription steroids within 1 year prior to Screening nasal steroids are permissible). A single short course (ie, less than 14 days) of systemic steroid therapy is allowed provided it is concluded more than 6 months prior to Screening.
    • History of diabetes
  8. Use of immunosuppressive agents, anticoagulants, or antiarrhythmics within 1 year prior to Screening. Nasal steroid use is permissible.
  9. Upper arms and thighs are with insufficient muscular tissue for IM injections or is obscured by tattoos or rash
  10. Use of any medications started within 30 days prior to Day -1, including prescription medications, nutritional supplements, and over-the-counter medications

    • Vitamin supplements are allowed
    • Recommended doses of acetaminophen are allowed, except for 24 hours prior to dosing
    • Recommended doses of non-steroidal anti-inflammatory drugs (NSAIDs) (eg, aspirin, ibuprofen) are also allowed, except for 7 days prior to dosing
  11. Positive hepatitis B surface antigen, hepatitis B core antigen, or hepatitis C antibody
  12. Positive urine drug test or cotinine (indicating active current smoking) at Screening or Day -1, positive alcohol breath test at Screening or on Day -1, or suspected/known drug abuse and/or alcohol use disorder
  13. Smoking or has used nicotine or nicotine-containing products (eg, snuff, nicotine patch, nicotine chewing gum, mock cigarettes, or inhalers) within 3 months before study drug dosing
  14. Dosing in any clinical research study evaluating another investigational drug or therapy within 30 days or at least 5 half-lives (whichever is longer) of receiving the investigational drug prior to Screening
  15. Progressive, unstable, or uncontrolled medical conditions that have required medical attention or changes to medication for medical reasons within 90 days prior to consent
  16. History of allergic reactions or hypersensitivity reactions to other therapeutic antibodies or immunoglobulins
  17. Receipt of any mAbs in the 12 months prior to Screening
  18. High blood pressure
  19. Women who are either pregnant or breast-feeding
  20. Vulnerable individuals (eg, military recruits, persons in compulsory detention, those with limited legal capacity)
  21. Receipt of immunoglobulins or any blood products within 90 days prior to consent or planned receipt during the study period
  22. Donation or loss of >500 mL of blood within 30 days or plasma within 7 days of Day 1; any planned donation of blood or plasma during the study period
  23. History of any malignant neoplasm within the last 5 years, with the exception of adequately treated localized or in situ non-melanoma carcinoma of the skin or the cervix
  24. Strenuous activity or contact sports within 48 hours before study drug dosing and through Day 8

26. History of relevant drug and/or food allergies

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Zapobieganie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Poczwórny

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny komparator: JST-018 Investigational Product
Monoclonal antibodies
Komparator placebo: JST-017 Placebo
Komparator placebo

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Safety and tolerability of of JST-018 administered intramuscularly (IM)
Ramy czasowe: From injection to Day 7
Incidence of solicited local (injection site) and systemic AEs post-injection through Day 7 (with the inpatient and outpatient participant diaries being collected on Day 3 and Day 8, respectively)
From injection to Day 7
Safety and tolerability of of JST-018 administered IM
Ramy czasowe: From injection to final visit at Week 48
Incidence of unsolicited AEs through end of study (EOS)
From injection to final visit at Week 48
Safety and tolerability of of JST-018 administered IM
Ramy czasowe: From injection to final visit at Week 48
Incidence of SAEs, medically attended AEs (MAAEs), and AEs of special interest (AESIs)
From injection to final visit at Week 48
Safety and tolerability of of JST-018 administered IM
Ramy czasowe: From injection to final visit at Week 48
Incidence of Clinically Significant Changes in Laboratory Values
From injection to final visit at Week 48
Safety and tolerability of JST-018 administered as IM
Ramy czasowe: From injection to final visit at Week 48
Incidence of Clinically Significant Changes in Vital Sign Measurements
From injection to final visit at Week 48
Safety and tolerability of JST-018 administered as IM
Ramy czasowe: From injection to final visit at Week 48
Incidence of Clinically Significant Changes in ECG results
From injection to final visit at Week 48

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Pharmacokinetic Cmax of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
Maximum observed concentration (Cmax)
From enrollment to the end of study at 48 weeks
Pharmacokinetic Tmax of JST-018
Ramy czasowe: Time Frame: From enrollment to the end of study at 48 weeks
Time to reach maximum observed concentration (Tmax)
Time Frame: From enrollment to the end of study at 48 weeks
Pharmacokinetic Tlast of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
The timepoint with the last quantifiable concentration (Tlast)
From enrollment to the end of study at 48 weeks
Pharmacokinetic AUC0-t of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
Area under the concentration versus time curve (AUC) from time 0 to the timepoint with the last quantifiable concentration (AUC0-t)
From enrollment to the end of study at 48 weeks
Pharmacokinetic AUC0-inf of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
AUC from time 0 extrapolated to infinity (AUC0-inf)
From enrollment to the end of study at 48 weeks
Pharmacokinetic t1/2 of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
Terminal elimination half-life (t1/2)
From enrollment to the end of study at 48 weeks
Pharmacokinetic CL/F of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
Apparent clearance after IM administration (CL/F)
From enrollment to the end of study at 48 weeks
Pharmacokinetic Vz/F of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
Apparent volume of distribution after IM administration (Vz/F)
From enrollment to the end of study at 48 weeks
Evaluation the effect of anti-drug antibodies (ADA)
Ramy czasowe: From enrollment to the end of study at 48 weeks
Effect of ADAs on pharmacokinetics of JST-018
From enrollment to the end of study at 48 weeks
Evaluate if and to what extent ADAs develop following a single dose of JST-018
Ramy czasowe: From enrollment to the end of study at 48 weeks
Proportion of participants with pre-existing ADAs and those who develop ADAs (treatment boosted and treatment induced) to JST-018
From enrollment to the end of study at 48 weeks

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

11 czerwca 2026

Zakończenie podstawowe (Szacowany)

9 listopada 2026

Ukończenie studiów (Szacowany)

4 października 2027

Daty rejestracji na studia

Pierwszy przesłany

7 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

14 maja 2026

Pierwszy wysłany (Rzeczywisty)

19 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

19 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

14 maja 2026

Ostatnia weryfikacja

1 maja 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • DDF4-CL101
  • MCDC No. W15QKN-16-9-1002 (Inny identyfikator: US Department of War)

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Opis planu IPD

This is a study in healthy volunteers. Individual participant data is not meaningful.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Badania kliniczne na Lek przeciwwirusowy

  • University Hospitals Cleveland Medical Center
    Washington University School of Medicine; Case Western Reserve University; Papua... i inni współpracownicy
    Zakończony
    Eliminacja Filariozy Limfatycznej przez Mass Drug Administration | Monitorowanie i ocena masowego podawania leków w przypadku Filariozy limfatycznej | Dopuszczalność masowego podawania leków w przypadku Filariozy limfatycznej
    Papua Nowa Gwinea

Badania kliniczne na Placebo

Subskrybuj