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Not Yet RecruitingNCT07532655

A Single Ascending Dose Study of SYH2082 Injection in Healthy Participants

A Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Dose of SYH2082 Injection in Healthy Participants

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
CSPC ZhongQi Pharmaceutical Technology Co., Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

To evaluate the safety and tolerability of single dose of SYH2082 Injection in healthy participants.

Conditions

Interventions

TypeNameDescription
DRUGSYH2082 InjectionA subcutaneous injection in the abdomen of the corresponding dose of SYH2082 Injection according to the assigned dose cohort.
DRUGPlaceboA subcutaneous injection in the abdomen of the corresponding dose of Placebo according to the assigned dose cohort.

Timeline

Start date
2026-04-14
Primary completion
2026-10-28
Completion
2027-02-09
First posted
2026-04-16
Last updated
2026-04-16

Source: ClinicalTrials.gov record NCT07532655. Inclusion in this directory is not an endorsement.