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A Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD4144 as Well as the Impact of AZD4144 on the Pharmacokinetics of Rosuvastatin and Furosemide in Healthy Participants

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NCT06491550

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
91actual
Sites
2
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-07-15actualWhen the study began enrolling
Primary completion2025-06-11actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-06-11actualThe whole study's end, after follow-up
First posted2024-07-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-07-04actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Participants

Interventions

  • Drug: AZD4144- Part A
  • Drug: Placebo- Part A
  • Drug: AZD4144- Part B
  • Drug: Placebo- Part B
  • Drug: Rosuvastatin and Furosemide- Part C
  • Drug: Rosuvastatin, Furosemide, and AZD4144 Part C

Primary outcomes

what the primary-completion date above is the date OF
Number of participants with adverse events (AEs) (Part A and Part B)
measured Part A: Day 1 to Day 10+3; Part B: Day 1 to Day 20+3.
Area under plasma concentration-time curve from time 0 to infinity (AUCinf) (Part C)
measured Treatment period 1: Day 1 to 3; Treatment period 2: Day 10 to 12.
Area under concentration-curve from time 0 to the last quantifiable concentration (AUClast) (Part C)
measured Treatment period 1: Day 1 to 3; Treatment period 2: Day 10 to 12.
Maximum observed drug concentration (Cmax) (Part C)
measured Treatment period 1: Day 1 to 3; Treatment period 2: Day 10 to 12.

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