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Study of SYH2062 Injection in Healthy Chinese Volunteers

Phase 1
Recruiting
Conditions
Healthy Chinese Volunteers
Interventions
Drug: SYH2062 injection
Drug: SYH2062-Matching placebo
Registration Number
NCT06842537
Lead Sponsor
CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.
Brief Summary

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

Detailed 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

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
46
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 informed consent.
  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) for males and 45 kg (inclusive) for females.
  4. Has Systolic blood pressure (SBP) ≥100 mmHg and <140 mmHg and diastolic blood pressure (DBP) ≥60 mmHg and <90 mmHg at screening;
  5. The subjects can communicate well with the investigators and complete the trial according to protocol.
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

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SYH2062 injectionSYH2062 injection-
SYH2062-Matching placeboSYH2062-Matching placebo-
Primary Outcome Measures
NameTimeMethod
Number of Participants with Adverse Events (AEs)up to approximately 12 months
Secondary Outcome Measures
NameTimeMethod
Change from Baseline in Blood Angiotensinogen (AGT) Levelup to approximately 12 months
Change from Baseline in in plasma renin concentrationup to approximately 12 months
Change from Baseline in in plasma renin activityup to approximately 12 months
Change from Baseline in in angiotensin Iup to approximately 12 months
Change from Baseline in in angiotensin IIup to approximately 12 months
Change from Baseline in in plasma aldosteroneup to approximately 12 months
To characterize the Cmax of single dose of SYH2062Up to Day 3
To characterize the AUC of single dose of SYH2062Up to Day 3
Number of Participants With Anti- SYH2062 Antibodiesup to approximately 3 months

Trial Locations

Locations (1)

Chinese Academy of Medical Science and Peking Union Medical College Hospital

🇨🇳

Beijing, Beijing, China

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