Clinical Trials Directory

Trials / Completed

CompletedNCT05336071

The Relative Bioavailability of INS068 Injection With Two Different Formulations in Healthy Subjects

Study on Bioavailability Study of INS068 Injection by Subcutaneous Injection of New and Old Formulations in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Jiangsu HengRui Medicine Co., Ltd. · Industry
Sex
Male
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The study is a single-centre, randomized, open, 2-period, 2-sequence crossover design clinical trial. It is planned to enroll 24 healthy male subjects. Subjects will receive INS068 injection on Day1 and Day8.

Conditions

Interventions

TypeNameDescription
DRUGINS068 injectionGroup A subjects were injected formulation T and formulation R of INS068 injection at Day1 and Day8.
DRUGINS068 injectionGroup B subjects were injected formulation R and formulation T of INS068 injection at Day1 and Day8.

Timeline

Start date
2022-05-12
Primary completion
2022-05-26
Completion
2022-06-02
First posted
2022-04-20
Last updated
2023-06-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05336071. Inclusion in this directory is not an endorsement.