Overview

A Phase I Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD5004

Status:
COMPLETED
Trial end date:
2025-04-20
Target enrollment:
Participant gender:
Summary
This is a Phase I, multicentre, single-dose, non-randomised, open-label, parallel-group study to examine the PK, safety, and tolerability of AZD5004 in male and female participants with severe renal impairment and moderate renal impairment (optional) compared with male and female participants with normal renal function.
Phase:
PHASE1
Details
Lead Sponsor:
AstraZeneca