A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SYH2053

NCT06229548 | Completed Phase 1

• 1 other identifier: SYH2053-001
• Study Type: interventional
• Target: 39
• Locations: 1 country
• Sites: 1

Brief Summary

This is a randomized, double-blind, placebo-controlled, single ascending dose (SAD) study of SYH2053 when administered subcutaneously to subjects with normal and elevated LDL-C.

Conditions

Hyperlipemia

Outcome Measures

Primary Outcomes (1)

• The Number of Participants with Treatment Related Adverse Events as Assessed by CTCAE v5.0

  The investigator will make an assessment of intensity for each AE and SAE reported during the study according to CTCAE V5.0

  Pre-dose and multiple timepoints no less than 57 days

Secondary Outcomes (16)

• The serum LDL-C level after dosing SYH2053

  Pre-dose and multiple timepoints no less than 57 days

• The serum PCSK9 level after dosing SYH2053

  Pre-dose and multiple timepoints no less than 57 days

• PK parameters (Cmax)

  Pre-dose and multiple timepoints up to 4 days

• PK parameters (Tmax)

  Pre-dose and multiple timepoints up to 4 days

• PK parameters (AUC)

  Pre-dose and multiple timepoints up to 4 days

Study Arms (2)

SYH2053 SAD experimental group

EXPERIMENTAL

Subjects in SAD experimental groups will receive a single subcutaneous injection of SYH2053 on Day 1.

Drug: SYH2053

Placebo SAD group

PLACEBO COMPARATOR

Subjects in SAD placebo groups will receive a single subcutaneous injection of placebo on Day 1.

Drug: Placebo

Interventions

SYH2053 DRUG

subcutaneous injection

SYH2053 SAD experimental group

Placebo DRUG

subcutaneous injection

Placebo SAD group

Eligibility Criteria

• Age: 18 Years - 60 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Subjects must give informed consent before the trial, fully understand the content, procedures and possible adverse reactions, and voluntarily sign a written informed consent.
• Sex: male or female subjects.
• Age of 18 - 60 years (inclusive).
• BMI: 18.6-28.5 kg/m\^2 (inclusive), with a minimum weight of 50 kg (inclusive) for male and 45 kg (inclusive) for female.
• During screening and baseline, LDL-C ≥100 mg/dL (2.6 mmol/L) and \< 190 mg/dL (4.9 mmol/L); TG ≤ 400 mg/dL (4.5 mmol/L); TC \< 278 mg/dL (7.2 mmol/L) in serum under fasting state;
• Subjects have no history of chronic or serious diseases or family history of early-onset coronary heart disease, including cardiovascular, liver, kidney, blood and lymphatic, endocrine, immune, psychiatric, neurological, and gastrointestinal systems, and are generally in good health.
• The subjects can communicate well with the investigators and complete the trial according to the protocol.

You may not qualify if:

• Allergic constitution or known history of allergy to the components of the study drug or similar drugs.
• Antibody drugs targeting PCSK9 have been used within 6 months prior to screening, oligonucleotides targeting PCSK9 have been used within 12 months prior to screening.
• There are currently medical disorders of clinical significance, including but not limited to, circulatory, hematological or hematopoietic diseases, respiratory, endocrine, urinary, digestive, neurological or psychiatric disorders, infections, tumors, severe trauma, or any other diseases that the investigator considers to be excluded or likely to interfere with the interpretation of the findings.
• Those who underwent major surgery within 6 months prior to initial administration, or who planned to undergo surgery during the study.
• Clinically significant abnormalities in vital signs, physical examination, electrocardiogram and laboratory examination.
• The estimated glomerular filtration rate (eGFR) during screening was \< 90 mL/min/1.73 m\^2 (calculated by simplified MDRD formula).
• During screening, any item of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin (TBIL), γ-glutamyltransferase (GGT), alkaline phosphatase (ALP) \> 1.5×ULN (retest once within 1 week allowed).
• During screening or baseline, subjects with prolonged QT/QTc interval (QTcF \> 450 ms in male, \> 470 ms in female).
• Subjects with non-negative test for any of HBsAg, HCV antibodies, syphilis antibodies, and HIV antibodies.
• Blood loss or blood donation of more than 200 mL within 3 months prior to administration (except for female menstrual period), and/or platelet donation within 2 weeks prior to administration.
• Use of any drug, supplement, vitamin or dietary supplement known to affect lipid metabolism within 28 days prior to administration; use of any drug for therapeutic purposes (except topical drugs with local effects) within 14 days prior to administration or within the 7 half-lives of the drug (whichever is longer).
• A history of drug abuse, and/or drug use within 3 months prior to screening, and/or habitual use of any psychotropic drug, including Chinese herbs.
• Positive urine drug screening.

Sponsors & Collaborators

• CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.: lead

Study Sites (1)

10 Chedaogou Rd.,Haidian District, Beijing, China

Beijing, Beijing Municipality, China

Location

MeSH Terms

Conditions

Hyperlipidemias

Condition Hierarchy (Ancestors)

Dyslipidemias; Lipid Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 20, 2023
• First Posted: January 29, 2024
• Study Start: January 8, 2024
• Primary Completion: December 23, 2024
• Study Completion: March 25, 2025
• Last Updated: April 4, 2025

Record last verified: 2023-12

Locations

CN (1)