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A Phase 1, Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ISM9528

6. November 2026 aktualisiert von: InSilico Medicine Hong Kong Limited

A Phase 1, Open-Label, Sequential Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Dose of ISM9528.

This is an open-label, phase 1, sequential study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single ascending dose of ISM9528 in healthy adult.

Studienübersicht

Status

Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

1

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Abu Dhabi Emirate
      • Abu Dhabi, Abu Dhabi Emirate, Vereinigte Arabische Emirate
        • Rekrutierung
        • Yas Clinic Khalifa City

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 65 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Männlich

Beschreibung

Inclusion Criteria:

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

  1. Male, ≥18 and ≤65 years of age.
  2. BMI >18.5 and <30.0 kg/m2 and body weight ≥50.0 kg for male.
  3. Non-smokers (no use of tobacco or nicotine products from 3 months prior to screening through the EOS visit).
  4. Healthy as defined the current protocol.
  5. Male participant who are not vasectomized for at least 3 months prior to dosing, and who are sexually active with a female partner of childbearing potential must be willing to use the acceptable contraceptive methods as defined the current protocol from the first dose and for 90 days after the last dose.
  6. Male participant (including men who have had a vasectomy) with a pregnant partner must agree to use a condom from the first dose and for 90 days after the last dose.
  7. Male participant must be willing not to donate sperm for 90 days after the last dose.
  8. Able to understand the study procedures and provide signed informed consent to participate in the study.

Exclusion Criteria:

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

  1. The participant had current evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease.
  2. Any clinically significant abnormal finding at physical examination.
  3. The participant had any condition possibly affecting drug absorption.
  4. Presence of fever (body temperature >37.5°C) (e.g., a fever associated with a symptomatic viral or bacterial infection) within 2 weeks prior to dosing.
  5. The participant had supine blood pressure (BP) >140 mm Hg (systolic) or >90 mm Hg (diastolic) following at least 5 minutes of supine rest.
  6. The participant has HR less than 50 or over 100 bpm.
  7. The participant had 12-lead ECG demonstrating corrected QT interval by Fridericia (QTcF) >450 msec or a QRS interval >120 msec at screening.
  8. The participant had any of the abnormalities as defined the current protocol in clinical laboratory tests at screening.
  9. C-SSRS score above Type 1 ideation at Screening.
  10. Clinically significant abnormal laboratory test results or positive serology test results for HBsAg, HCV antibody, or HIV antibody at Screening.
  11. Positive urine drug screen, urine cotinine test, or urine alcohol test.
  12. History of significant allergic reactions to any drug.
  13. History of any central nervous system (CNS) disorder or history of seizure of any cause.
  14. History of drug abuse within 1 year prior to screening or recreational use of soft drugs within 1 month or hard drugs within 3 months prior to screening.
  15. History of alcohol abuse within 1 year prior to screening or regular use of alcohol within 6 months prior to screening that exceeds 10 units for women or 15 units for men of alcohol per week or who are unwilling to abstain from alcohol during the study.
  16. History of active tuberculosis or presence of active or latent tuberculosis at Screening.
  17. History of clinically significant opportunistic infection.
  18. History of serious local infection or systemic infection within 3 months prior to screening.
  19. Use of medications for the timeframes specified below, with the exception of medications exempted by the Investigator on a case-by-case basis because they are judged unlikely to affect the PK profile of the study drug or participant safety.
  20. Participation in a clinical research study involving the administration of an investigational or marketed drug or device within 30 days prior to the first dosing, administration of a biological product in the context of a clinical research study within 90 days prior to the first dosing, or concomitant participation in an investigational study involving no drug or device administration.
  21. Donation of plasma within 7 days prior to dosing or donation or loss of 500 mL or more of whole blood within 8 weeks prior to dosing.
  22. Participant who consumed excessive amounts of tea, coffee, or caffeine-containing beverages within 3 months prior to screening, or who are unwilling to abstain from coffee during the study.
  23. Participant who have consumed specific foods/beverages within 48 hours prior to dosing.
  24. The participant had a history of cancer with the exception of adequately treated basal cell or squamous cell carcinoma of the skin.
  25. Withdrawal of the hand before 15 seconds of immersion or after 120 seconds in the cold water bath in any cold pressor test during the Screening familiarization sessions.
  26. The Lower PTT < 50% of the higher PTT in the second and third CPT assessments among the three cold pressor tests performed during Screening.
  27. Participant who have difficulty in venous blood collection or have a history of needle and blood fainting.
  28. Participant with dysphagia, or who are unable to swallow the study drug whole as judged by the investigator.
  29. Any reason which, in the opinion of the Investigator, would prevent the participant from participating in the study.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Sequenzielle Zuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: ISM9528 capsule will be administered orally with three single doses in a healthy male participant.

ISM9528 capsules will be orally administered as per the schedule specified in the protocol.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
The incidence of Adverse Events (AEs) after single dose of ISM9528 capsules.
Zeitfenster: Up to 28 days after last dose.

To evaluate the safety and tolerability of ISM9528.

Up to 28 days after last dose.
The incidence of abnormalities in vital signs measurements, 12-lead ECG, physical examinations,CNS safety battery,C-SSRS(Columbia Suicidality Severity Rating Scale) and clinical laboratory test.
Zeitfenster: Up to 48 hours after last dose.

To evaluate the safety and tolerability of ISM9528.

Up to 48 hours after last dose.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Maximal observed plasma concentration (Cmax).
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Time when the maximal concentration is observed (Tmax).
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Area under the concentration-time curve from time zero to the last observed concentration (AUC0-t).
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Area under the concentration-time curve from time zero to infinity (extrapolated)(AUC0-inf).
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Terminal elimination half-life(T½).
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Apparent clearance (CL/F).
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Apparent Volume of Distribution(Vz/F)
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Percentage of AUC0-inf Obtained by Extrapolation(%AUCex).
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.
Terminal Elimination Rate Constant(Kel)
Zeitfenster: From pre-dose through at least 48 hours post-dose, depending on the dose period.

To characterize plasma PK of ISM9528 after each single dose.

From pre-dose through at least 48 hours post-dose, depending on the dose period.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

29. Oktober 2026

Primärer Abschluss (Geschätzt)

3. Dezember 2026

Studienabschluss (Geschätzt)

3. Dezember 2026

Studienanmeldedaten

Zuerst eingereicht

6. November 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

6. November 2026

Zuerst gepostet (Tatsächlich)

12. November 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

12. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

6. November 2026

Zuletzt verifiziert

1. November 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Andere Studien-ID-Nummern

  • ISM9528-000

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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