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A Phase 1, Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ISM8969

17. juni 2026 opdateret af: InSilico Medicine Hong Kong Limited

A Phase 1, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Oral Doses of ISM8969 in Healthy Adult and Elderly Participants and Obese Adult Participants at Risk of Cardiovascular Disease

This is a single center, phase 1, randomized, double-blind, placebo-controlled sequential study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple ascending oral doses of ISM8969 in healthy adults and elderly participants and obese adult participants at risk of cardiovascular disease.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

100

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

    • Victoria
      • Melbourne, Victoria, Australien
        • Rekruttering
        • Nucleus Network Pty Ltd.

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

Participants must meet all the following criteria to be included in the study:

Inclusion criteria 1~4 are only for the healthy participants in the SAD and MAD study:

  1. Male or female participants, including adult participants (≥18 and <65 years of age) for the SAD cohorts 1-6 and MAD cohorts 1-3, and elderly participants (≥65 and ≤80 years of age) for MAD cohort 4.
  2. Body mass index (BMI) >18.5 and <30.0 kg/m2 and body weight ≥50.0 kg for males and ≥45.0 kg for females.
  3. Non-smokers (no use of tobacco or nicotine products within 1 month prior to screening).
  4. Healthy as defined the current protocol.

    Inclusion criteria 5~9 are only for the obese participants at risk of cardiovascular disease in MAD study):

  5. Male or female, ≥18 and ≤65 years of age.
  6. 30.0 kg/m2 ≤ BMI < 42.0 kg/m2.
  7. No change in body weight or self-reported change of less than 5.0% within 3 months before screening.
  8. Presence of 1 or more risk factors for cardiovascular disease such as hypertension, hyperlipidemia. If present, must be controlled with stable medication dose/therapy (defined as a stable medication dose/therapy for 3 months or longer).
  9. hsCRP ≥3 mg/L.

Exclusion Criteria:

Participants for whom any of the following applies will be excluded from the study:

  1. Columbia suicide severity rating scale (C-SSRS) score above Type 1 ideation.
  2. Positive serology test results for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antigen and antibody, treponema pallidum antibody or QuantiFERON®-TB test at screening.
  3. Positive pregnancy test or lactating female participant.
  4. History of any central nervous system (CNS) disorder or history of seizure of any cause.
  5. Clinically significant 12-lead ECG, physical examination, vital signs or laboratory abnormalities at screening, including but not limited to defined in the protocol.
  6. History of significant cardiovascular or cerebrovascular disease within 6 months before screening, including but not limited to defined in the protocol.
  7. History of an active or untreated malignancy or are in remission from a clinically significant malignancy (other than basal- or squamous-cell skin cancer, or in situ carcinomas of the cervix) for less than 5 years; or there is a potential malignancy during screening.
  8. Participation in a clinical research study involving the administration of an investigational or marketed drug or device within 30 days (or 5 half-lives, whichever is longer) prior to the first dosing, administration of a biological product in the context of a clinical research study within 90 days (or 5 half-lives, whichever is longer) prior to the first dosing, or concomitant participation in an investigational study involving no drug or device administration.
  9. Presence of contraindication to lumbar puncture or lumbar catheter as judged by Investigator.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Healthy adults in SAD cohorts will receive ISM8969 or placebo orally up to 6 single-dose levels.
Administration: Oral
Eksperimentel: Healthy adults and elderly participants in MAD cohorts will receive ISM8969 or placebo up to14 days.
Administration: Oral
Eksperimentel: Obese adult participants will receive ISM8969 or placebo orally up to 14 days.
Administration: Oral

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
The incidence of Adverse Events (AEs) after single or multiple doses of ISM8969 tablets.
Tidsramme: Up to 14 days after last dose.
To evaluate the safety and tolerability of ISM8969.
Up to 14 days after last dose.
Number of Participants with Clinical Laboratory Abnormalities, and Abnormalities in Vital Signs, Physical Examinations,12-lead ECG
Tidsramme: Up to 14 days after last dose.
Vital signs (blood pressure, heart rate, respiratory rate, and oral temperature), physical examinations, 12-lead ECG(heart rate , PR interval, QT interval, RR interval, QTcF and QRS),and clinical laboratory tests (hematology, biochemistry, coagulation and urinalysis, etc.)
Up to 14 days after last dose.
C-SSRS Score(Type 1 to Type 5)
Tidsramme: Up to 14 days after last dose.
The C-SSRS(Columbia Suicidality Severity Rating Scale) is a suicidal ideation and behavior rating scale to evaluate suicide risk, higher C-SSRS scores mean a worse outcome.
Up to 14 days after last dose.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Maximal observed plasma concentration (Cmax).
Tidsramme: Day 1 and Day 14 after dose.
To characterize plasma PK of ISM8969 after the first dose and at steady state.
Day 1 and Day 14 after dose.
Time when the maximal concentration is observed (Tmax).
Tidsramme: Day 1 and day 14 after dose.
To characterize plasma PK of ISM8969 after the first dose and at steady state.
Day 1 and day 14 after dose.
Area under the concentration-time curve from time zero to the last observed concentration (AUC0-t).
Tidsramme: Day 3 and Day 17 after dose.
To characterize plasma PK of ISM8969 after the first dose and at steady state.
Day 3 and Day 17 after dose.
Area under the concentration-time curve from time zero to infinity (extrapolated)(AUC0-inf).
Tidsramme: Day 3 and Day 17 after dose.
To characterize plasma PK of ISM8969 after single and multiple dose administration.
Day 3 and Day 17 after dose.
Terminal elimination half-life(T½).
Tidsramme: Day 3 and Day 17 after dose.
To characterize plasma PK of ISM8969 after single and multiple dose administration.
Day 3 and Day 17 after dose.
Apparent clearance (CL/F).
Tidsramme: Day 1 and Day 14 after dose.
To characterize plasma PK of ISM8969 after single and multiple dose administration.
Day 1 and Day 14 after dose.
Apparent volume of distribution (V/F).
Tidsramme: Day 1 and day 14 after dose.
To characterize plasma PK of ISM8969 after single and multiple dose administration.
Day 1 and day 14 after dose.
Maximal observed cerebrospinal fluid(CSF) concentration (Cmax,csf).
Tidsramme: Day 14 after dose.
To characterize cerebrospinal fluid(CSF) PK of ISM8969 at steady state.
Day 14 after dose.
Accumulation ratio (Day 14 : Day 1) (Racc).
Tidsramme: Day 14 after dose.
To characterize the PK of ISM8969.
Day 14 after dose.
Change from baseline in the concentration of blood high sensitivity C-reactive protein(hsCRP).
Tidsramme: Day 14 after dose.
Concentration of hsCRP will be measured and reported.
Day 14 after dose.
Minimal observed concentration at steady-state (Cmin,ss).
Tidsramme: Day 14 before the last dose.
To characterize plasma PK of ISM8969.
Day 14 before the last dose.
Minimal observed cerebrospinal fluid(CSF) concentration at steady-state (Cmin,ss).
Tidsramme: Day 14 before the last dose.
To characterize PK of ISM8969 in cerebrospinal fluid (CSF).
Day 14 before the last dose.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

15. juni 2026

Primær færdiggørelse (Anslået)

29. januar 2027

Studieafslutning (Anslået)

31. marts 2027

Datoer for studieregistrering

Først indsendt

10. april 2026

Først indsendt, der opfyldte QC-kriterier

6. maj 2026

Først opslået (Faktiske)

12. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

17. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • ISM8969-101

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ja

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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