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Not Yet RecruitingNCT07241910

A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SYH2061

A Phase I, Single-Center, Randomized, Double-Blind, Placebo-Controlled, Single-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of SYH2061 in Healthy Subjects

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a randomized, double-blind, placebo-controlled, single-ascending dose study in healthy subjects to evaluate the safety, tolerability, PK, and PD of SYH2061.

Conditions

Interventions

TypeNameDescription
DRUGSYH2061subcutaneous injection
DRUGPlacebosubcutaneous injection

Timeline

Start date
2025-11-24
Primary completion
2026-11-24
Completion
2027-04-01
First posted
2025-11-21
Last updated
2025-11-21

Source: ClinicalTrials.gov record NCT07241910. Inclusion in this directory is not an endorsement.

A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SYH2061 (NCT07241910) · Clinical Trials Directory