Study S003267
An Open-Label, Parallel-Group, Single-Dose Pharmacokinetic Study of HRS-4729 Injection in Healthy Participants and Patients With Renal Impairment
Registration
Registered primary outcomes
- Cmax [assessed up to approximately 4 weeks post-dose;]
- AUC0-t [assessed up to approximately 4 weeks post-dose]
- AUC0-inf. [assessed up to approximately 4 weeks post-dose]
Linked records (0)
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