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

2026年11月6日 更新者: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.

調査の概要

状態

募集

介入・治療

研究の種類

介入

入学 (推定)

1

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Abu Dhabi Emirate
      • Abu Dhabi、Abu Dhabi Emirate、アラブ首長国連邦
        • 募集
        • Yas Clinic Khalifa City

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~65年 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

男

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:順次割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
The incidence of Adverse Events (AEs) after single dose of ISM9528 capsules.
時間枠: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.
時間枠:Up to 48 hours after last dose.

To evaluate the safety and tolerability of ISM9528.

Up to 48 hours after last dose.

二次結果の測定

結果測定
メジャーの説明
時間枠
Maximal observed plasma concentration (Cmax).
時間枠: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).
時間枠: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).
時間枠: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).
時間枠: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).
時間枠: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).
時間枠: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)
時間枠: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).
時間枠: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)
時間枠: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.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年10月29日

一次修了 (推定)

2026年12月3日

研究の完了 (推定)

2026年12月3日

試験登録日

最初に提出

2026年11月6日

QC基準を満たした最初の提出物

2026年11月6日

最初の投稿 (実際)

2026年11月12日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月12日

QC基準を満たした最後の更新が送信されました

2026年11月6日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

キーワード

その他の研究ID番号

  • ISM9528-000

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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