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

2026년 11월 6일 업데이트: 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.

연구 개요

상태

모병

연구 유형

중재적

등록 (추정된)

1

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Abu Dhabi Emirate
      • Abu Dhabi, Abu Dhabi Emirate, 아랍 에미리트
        • 모병
        • Yas Clinic Khalifa City

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

예

연구 대상 성별

남성

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
The incidence of Adverse Events (AEs) after single dose of ISM9528 capsules.
기간: 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.
기간: Up to 48 hours after last dose.

To evaluate the safety and tolerability of ISM9528.

Up to 48 hours after last dose.

2차 결과 측정

결과 측정
측정값 설명
기간
Maximal observed plasma concentration (Cmax).
기간: 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).
기간: 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).
기간: 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).
기간: 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).
기간: 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).
기간: 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)
기간: 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).
기간: 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)
기간: 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.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 10월 29일

기본 완료 (추정된)

2026년 12월 3일

연구 완료 (추정된)

2026년 12월 3일

연구 등록 날짜

최초 제출

2026년 11월 6일

QC 기준을 충족하는 최초 제출

2026년 11월 6일

처음 게시됨 (실제)

2026년 11월 12일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 12일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 6일

마지막으로 확인됨

2026년 11월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • ISM9528-000

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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