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Study details
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A Study to Investigate Safety and How AZD4248 Works

AstraZeneca
NCT IDNCT07024823ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

124

Study length

about 11 months

Ages

18–75

Locations

5 sites in CA, IL, MI +2

About this study

Researchers are testing the safety, how well AZD4248 works in the body (pharmacokinetics), and how it affects the body (pharmacodynamics) when given as a pill or injection. The trial also looks at whether people with kidney disease can measure creatinine at home.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take AZD4248
  • 2.Take Placebo
PhasePhase 1
Primary goalPart D: Intra- and inter-participant variability of estimated glomerular filtration rate (eGFR) derived from home self-testing device measurements

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low11%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Part D: Intra- and inter-participant variability of estimated glomerular filtration rate (eGFR) derived from home self-testing device measurements, Parts A, B, and C: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)

Secondary: Accumulation ratio for AUC (Rac AUC), Accumulation ratio for Cmax (Rac Cmax), Apparent total body clearance (CL/F), Dose normalized Cmax (Cmax/D), Individual and cumulative amount of unchanged drug excreted into urine from time t1 to time t2 [Ae(t1-t2)], Maximum observed drug concentration (Cmax), Part D: Estimated glomerular filtration rate (eGFR), Part D: Intra- and inter-participant variability of eGFR derived from laboratory measurements

Body systems

Renal