Study S001738
Investigation on Safety, Tolerability and Pharmacokinetics of Liraglutide-depot in Healthy Subjects. A Randomised, Double-blind, Placebo-controlled Trial Investigating Subcutaneously Single Dose Escalation of a Sustained Release Formulation of Liraglutide Lysine in Healthy Male Subjects
Registration
Registered primary outcomes
- Number of Treatment Emergent Adverse Events (TEAEs) [Day 0 and up to 21 days after treatment]
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