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
| Type | Name | Description |
|---|---|---|
| DRUG | INS068 injection | Group A subjects were injected formulation T and formulation R of INS068 injection at Day1 and Day8. |
| DRUG | INS068 injection | Group 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.