A Study to Evaluate Safety, Tolerability and pK of Semaglutide ER Injectable Suspension in Healthy, Adult Human Subjects
NCT06422624 · Not yet recruiting
Last updated 2026-05-28This clinical trial tests the safety, tolerability, and how the body processes a long-acting injectable form of semaglutide in healthy adults.
Status Not yet recruiting Approved but enrollment has not started.
Phase Phase 1 Checks safety and dosing in a small group.
Type Interventional (clinical trial)
Design Non-randomized, open-label (no blinding) treatment study
Participants 14 people Planned (estimated).
Who can join Ages 18–45 · all sexes Healthy volunteers accepted.
Timeline Started 2024-08 · est. completion 2024-11
What this study is testing ClinicalTrials.gov NCT06422624 ↗
Description as written by the study sponsor.
The purpose of the trail is to evaluate the safety, tolerability and pharmacokinetics of a single escalated doses of semaglutide extended-release injectable suspension in healthy adult, human study participants under fasting condition.
Treatments tested
- Semaglutide Extended-release for Injectable Suspension, 1 mg Drug
Singel-dose; Subcutaneous
- Semaglutide Extended-release for Injectable Suspension, 4 mg Drug
Singel-dose; Subcutaneous
- Semaglutide Extended-release for Injectable Suspension, 8 mg Drug
Singel-dose; Subcutaneous
| Main thing measured | Cmax |
|---|---|
| Sponsor | Bostal Drug Delivery Co., Ltd |
| Conditions studied | Diabetes Mellitus, Type 2 |
| GLP-1 drugs | semaglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT06422624 ↗