- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07595458
Phase 1 Study on the Safety, Tolerability, and Pharmacokinetics of JST-018 in Healthy Adults
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
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
- Name: Nels Royer
- Telefonnummer: (206)651-5094
- E-Mail: jeb.clinicaltrials@evotec.com
Studienorte
-
-
Nevada
-
Las Vegas, Nevada, Vereinigte Staaten, 89113
- PPD Las Vegas Clinical Research Unit
-
Kontakt:
- Telefonnummer: (877) 362-2608
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Healthy men or women 18 to 55 years of age
- BMI between 18 and 32 kg/m2
- Negative serum pregnancy test
- 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
- In good general health as determined by medical history, exams and tests
Exclusion Criteria:
- Acute illness or fever (≥100.4°F) within 7 days prior to dosing
- Any history of receiving treatment, vaccine, or monoclonal antibodies (mAbs) against smallpox, monkeypox, or other orthopox viruses.
- 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.
- Any medical condition for which IM injections would be contraindicated in the opinion of the investigator (eg, bleeding disorders, anticoagulant therapy, and severe thrombocytopenia)
- History of congenital or acquired immunodeficiency syndrome, , including positive human immunodeficiency virus (HIV-1/-2) antibody result
- Prior solid organ or bone marrow transplant
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
- Use of immunosuppressive agents, anticoagulants, or antiarrhythmics within 1 year prior to Screening. Nasal steroid use is permissible.
- Upper arms and thighs are with insufficient muscular tissue for IM injections or is obscured by tattoos or rash
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
- Positive hepatitis B surface antigen, hepatitis B core antigen, or hepatitis C antibody
- 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
- 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
- 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
- Progressive, unstable, or uncontrolled medical conditions that have required medical attention or changes to medication for medical reasons within 90 days prior to consent
- History of allergic reactions or hypersensitivity reactions to other therapeutic antibodies or immunoglobulins
- Receipt of any mAbs in the 12 months prior to Screening
- High blood pressure
- Women who are either pregnant or breast-feeding
- Vulnerable individuals (eg, military recruits, persons in compulsory detention, those with limited legal capacity)
- Receipt of immunoglobulins or any blood products within 90 days prior to consent or planned receipt during the study period
- 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
- 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
- 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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Vervierfachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Aktiver Komparator: JST-018 Investigational Product
|
Monoclonal antibodies
|
|
Placebo-Komparator: JST-017 Placebo
|
Placebo-Komparator
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Safety and tolerability of of JST-018 administered intramuscularly (IM)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: From injection to final visit at Week 48
|
Incidence of Clinically Significant Changes in Vital Sign Measurements
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From injection to final visit at Week 48
|
|
Safety and tolerability of JST-018 administered as IM
Zeitfenster: From injection to final visit at Week 48
|
Incidence of Clinically Significant Changes in ECG results
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From injection to final visit at Week 48
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Pharmacokinetic Cmax of JST-018
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
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Pharmacokinetic AUC0-inf of JST-018
Zeitfenster: From enrollment to the end of study at 48 weeks
|
AUC from time 0 extrapolated to infinity (AUC0-inf)
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From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic t1/2 of JST-018
Zeitfenster: 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
Zeitfenster: From enrollment to the end of study at 48 weeks
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Apparent clearance after IM administration (CL/F)
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From enrollment to the end of study at 48 weeks
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Pharmacokinetic Vz/F of JST-018
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
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From enrollment to the end of study at 48 weeks
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- DDF4-CL101
- MCDC No. W15QKN-16-9-1002 (Andere Kennung: US Department of War)
Plan für individuelle Teilnehmerdaten (IPD)
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Beschreibung des IPD-Plans
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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