Study S000701
A Randomized, Parallel-Group Study to Assess the Safety, Tolerability, and Pharmacokinetics of Exenatide Implant
Registration
Registered primary outcomes
- Area under the plasma concentration-time curve (AUC) [9 weeks]
- Maximum plasma concentration observed (Cmax) [9 weeks]
- Time to maximum plasma concentration observed (Tmax) [9 weeks]
- Adverse events [9 weeks]
Linked records (0)
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No records link to this registration yet.