drugset / Trial / NCT06422624

A Study to Evaluate Safety, Tolerability and pK of Semaglutide ER Injectable Suspension in Healthy, Adult Human Subjects

NCT06422624

Phase 1 Unknown 14 enrolled Bostal Drug Delivery Co., Ltd
Non-randomizedSequentialOpen-labelTreatment

Summary

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.

Timeline

Start
2024-08
Primary completion
2024-11
Completion
2024-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Semaglutide Peptide 1 mg Subcutaneous
Subject Semaglutide Peptide 4 mg Subcutaneous
Subject Semaglutide Peptide 8 mg Subcutaneous