Study of SYH2062 Injection in Healthy Chinese Volunteers

Last updated: March 20, 2025
Sponsor: CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.
Overall Status: Active - Recruiting

Phase

1

Condition

N/A

Treatment

SYH2062-Matching placebo

SYH2062 injection

Clinical Study ID

NCT06842537
SYH2062-001
  • Ages 18-55
  • All Genders

Study Summary

The purpose of this study is to evaluate the safety, tolerability, efficacy, pharmacodynamics and pharmacokinetics of SYH2062 injection in healthy Chinese volunteers

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Subjects must give informed consent before the trial, fully understand the content,process and possible adverse reactions, and voluntarily sign a written informedconsent.

  2. Age of 18 - 55 years (inclusive).

  3. BMI: 19.0-26.0 kg/m^2 (inclusive), with a minimum weight of 50 kg (inclusive) formales and 45 kg (inclusive) for females.

  4. Has Systolic blood pressure (SBP) ≥100 mmHg and <140 mmHg and diastolic bloodpressure (DBP) ≥60 mmHg and <90 mmHg at screening;

  5. The subjects can communicate well with the investigators and complete the trialaccording to protocol.

Exclusion

Exclusion Criteria:

Allergic constitution, or known history of allergy to the components of the study drug or similar drugs.

2 Subjects with the following diseases of clinical significance (including but not limited to diseases of the circulatory system, diseases of the blood or hematopoietic system, diseases of the respiratory system, diseases of the endocrine system, diseases of the urinary system, diseases of the digestive system, neurological or mental diseases, infections, tumors, serious injuries).

3 Those who underwent major surgery within 6 months prior to initial administration, or who planned to undergo surgery during the study.

4 Blood loss or blood donation of more than 200 mL within 3 months prior to initial administration (except for female menstrual period), and/or platelet donation within 2 weeks prior to initial administration.

5 Positive urine drug screening. 6 Those who smoked more than 5 cigarettes per day within 3 months prior to screening and/or did not agree to refrain from using any tobacco products during hospitalization.

7 Regular drinkers within 6 months prior to screening, i.e., those who drank more than 14 units of alcohol per week, and/or those who could not stop drinking alcohol during their hospitalization, and/or test positive for breath alcohol.

Study Design

Total Participants: 42
Treatment Group(s): 2
Primary Treatment: SYH2062-Matching placebo
Phase: 1
Study Start date:
March 01, 2025
Estimated Completion Date:
December 31, 2025

Study Description

A Phase 1, randomized, double-Blind, placebo-Controlled study to evaluate the safety, tolerability, pharmacokinetic and pharmacodynamic characteristics of SYH2062 injection after a single administration in healthy subjects

Connect with a study center

  • Chinese Academy of Medical Science and Peking Union Medical College Hospital

    Beijing, Beijing
    China

    Active - Recruiting

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