drugset / Trial / NCT05268237

Safety, Tolerability and Preliminary Efficacy of Sublingual Liraglutide in Patients With Type 2 Diabetes Mellitus

NCT05268237

Phase 1/2 Recruiting 15 enrolled Biolingus Chinese University of Hong Kong · collab
RandomizedSequentialDouble-blindTreatment

Summary

This is a phase Ib/IIa, single ascending dose study of the safety, tolerability and preliminary efficacy of sublingual (SL) Liraglutide in patients with type 2 diabetes mellitus (T2DM).

Timeline

Start
2023-04-25
Primary completion
2025-12
Completion
2026-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Liraglutide Peptide 3 mg Other
Subject Liraglutide Peptide 12 mg Other
Subject Liraglutide Peptide 30 mg Other