drugset / Trial / NCT06742762

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

NCT06742762

Phase 1 Completed 16 enrolled AstraZeneca
Non-randomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2024-12-17
Primary completion
2025-04-20
Completion
2025-04-20

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD5004 Unknown Oral