drugset / Trial / NCT07024823

A Study to Investigate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD4248 in Healthy Participants and Participants With Chronic Kidney Disease and Type 2 Diabetes and to Assess Home Measurements of Creatinine in a Non Interventional Cohort

NCT07024823 ↗

Phase 1 Recruiting 124 enrolled AstraZeneca Parexel · collab
RandomizedSequentialDouble-blindTreatment

Summary

This study will evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single ascending doses (SAD) and multiple ascending doses (MAD) of AZD4248 administered as an oral solution and intravenous (IV) infusion. Additionally, the study investigates the non-interventional feasibility of home measurement of serum creatinine in participants with diabetic kidney disease (DKD).

Timeline

Start
2025-06-09
Primary completion
2026-12-25
Completion
2026-12-25

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD4248 Unknown — Oral