Study S002051
A Phase 2a Dose-Finding Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of NLY01, a PEGylated Exenatide, When Administered as a Single Dose in Subjects With Type 2 Diabetes
Registration
Registered primary outcomes
- Number of participants with Treatment Emergent Adverse Events [35 days]
- Number of Incidences of Adverse Events [35 days]
- Plasma glucose [24 hours]
- Change in serum insulin [24 hours]
- Change in plasma glucagon [24 hours]
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