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

3 augustus 2026 bijgewerkt door: 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

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

48

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

    • Nevada
      • Las Vegas, Nevada, Verenigde Staten, 89113
        • Werving
        • PPD Las Vegas Clinical Research Unit
        • Contact:
          • Telefoonnummer: (877) 362-2608

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Preventie
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Actieve vergelijker: JST-018 Investigational Product
Monoclonal antibodies
Placebo-vergelijker: JST-017 Placebo
Placebo-vergelijker

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Safety and tolerability of of JST-018 administered intramuscularly (IM)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: From injection to final visit at Week 48
Incidence of Clinically Significant Changes in ECG results
From injection to final visit at Week 48

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Pharmacokinetic Cmax of JST-018
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

23 juni 2026

Primaire voltooiing (Geschat)

9 november 2026

Studie voltooiing (Geschat)

4 oktober 2027

Studieregistratiedata

Eerst ingediend

7 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

14 mei 2026

Eerst geplaatst (Werkelijk)

19 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

5 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

3 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

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

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

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

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Ja

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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