Study S000117
Investigation on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of a Long-acting GLP-1 Analogue in Healthy Male Subjects
Registration
Registered primary outcomes
- Frequency of adverse events (AEs) [from the first trial related activity (screening visit) and until completion of the post treatment follow-up visit 91-105 days after first dose]
Linked records (0)
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