Clinical Trials Directory

Trials / Completed

CompletedNCT06995001

Phase I Study on the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a Single Subcutaneous Injection of SHR-2173 in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Guangdong Hengrui Pharmaceutical Co., Ltd · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The study is being conducted to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics and immunogenicity of a single dose of SHR-2173 by subcutaneous injection.

Conditions

Interventions

TypeNameDescription
DRUGSHR-2173SHR-2173 injection dose 1;
DRUGSHR-2173 ;PlaceboSHR-2173 injection dose 2 ;Pacebo dose 2
DRUGSHR-2173 ;PlaceboSHR-2173 injection dose 3 ;Pacebo dose 3
DRUGSHR-2173 ;PlaceboSHR-2173 injection dose 4 ;Pacebo dose 4
DRUGSHR-2173 ;PlaceboSHR-2173 injection dose 5 ;Pacebo dose 5

Timeline

Start date
2024-04-28
Primary completion
2024-11-28
Completion
2024-11-28
First posted
2025-05-29
Last updated
2025-05-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06995001. Inclusion in this directory is not an endorsement.