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Study identifier: NCT07024823 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Chronic Kidney Disease  ·  Sponsor: AstraZeneca

PhasePhase 1
Planned participants124
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersYes

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

AstraZeneca Clinical Study Information Center  ·  1-877-240-9479  ·  information.center@astrazeneca.com

Always discuss trial participation with your own doctor first.

Locations (5)

Research SiteGlendale, California, United StatesRecruiting
Research SiteChicago, Illinois, United StatesRecruiting
Research SiteAnn Arbor, Michigan, United StatesActive Not Recruiting
Research SiteSaint Paul, Minnesota, United StatesRecruiting
Research SiteSan Antonio, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07024823