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Not Yet RecruitingNCT07264335

A Study on the Bioavailability of SHR-1819 Injection Administered Subcutaneously Using Different Injection Devices in Healthy Subjects

A Randomized, Open-Label, Parallel-Group Clinical Study to Evaluate the Bioavailability and Safety of Subcutaneous SHR-1819 Injection Administered Using Different Injection Devices in Healthy Subjects

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

Summary

This study is a randomized, parallel-group, open-label Phase I clinical trial designed to compare the bioavailability and safety of subcutaneous SHR-1819 injection administered via different injection devices in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGSHR-1819 InjectionSHR-1819 injection.

Timeline

Start date
2025-12-01
Primary completion
2026-03-01
Completion
2026-03-01
First posted
2025-12-04
Last updated
2025-12-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07264335. Inclusion in this directory is not an endorsement.

A Study on the Bioavailability of SHR-1819 Injection Administered Subcutaneously Using Different Injection Devices in He (NCT07264335) · Clinical Trials Directory