Condition: Chronic Kidney Disease · Sponsor: AstraZeneca
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.
AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com
Always discuss trial participation with your own doctor first.
| Research Site | Glendale, California, United States | Recruiting |
| Research Site | Chicago, Illinois, United States | Recruiting |
| Research Site | Ann Arbor, Michigan, United States | Active Not Recruiting |
| Research Site | Saint Paul, Minnesota, United States | Recruiting |
| Research Site | San Antonio, Texas, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07024823