LivingGLP1
Study S001751

A Phase Ib/IIa, Single Ascending Dose Study of the Safety, Tolerability and Preliminary Efficacy of Sublingual Liraglutide in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT05268237
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1; PHASE2
Masking
DOUBLE
Status
RECRUITING
Enrollment
15
Start
2023-04-25
Primary completion
2025-12
Lead sponsor
Biolingus
Conditions
Diabete Type 2
Interventions
DRUG:Liraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Incidence, nature and severity of adverse events [Through study completion, an average of 6 weeks]

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