Study S003295

A Phase I, Multicentre, Single-Dose, Non-Randomised, Open-Label, Parallel Group Study to Investigate the Effect of Renal Impairment on the Pharmacokinetics, Safety, and Tolerability of AZD5004

ClinicalTrials.gov record

Registration

Registration: NCT06742762
Study type: INTERVENTIONAL
Allocation: NON_RANDOMIZED
Phase: PHASE1
Masking: NONE
Status: COMPLETED
Enrollment: 16
Start: 2024-12-17
Primary completion: 2025-04-20
Lead sponsor: AstraZeneca
Conditions: Renal Impairment
Interventions: DRUG:AZD5004
Results posted: FALSE
Individual participant data sharing: YES

Registered primary outcomes

AUCinf [Day 1 to Day 5]
AUClast [Day 1 to Day 5]
Cmax [Day 1 to Day 5]

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