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A Study to Investigate Multiple Ascending Doses and Relative Bioavailability of AZD5004 in Healthy Participants

← catalyst calendar

NCT06555822

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · Single · Treatment
Enrollment
31actual
Sites
1
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
Start2024-08-15actualWhen the study began enrolling
Primary completion2025-03-06actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-03-06actualThe whole study's end, after follow-up
First posted2024-08-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-03-17actualThe 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: AZD5004 — also filed as ECC5004
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Part A: Number of participants with adverse events (AEs) and serious adverse events (SAEs)
measured From screening (Day -28) to last follow up visit (Day 120)
Part B: Maximum observed plasma (peak) drug concentration (Cmax) of AZD5004
measured From Day 1 (Treatment Period 1) to Day 13 (end of Treatment Period 2)
Part B: Area under the concentration-curve from time zero to the last quantifiable concentration (AUClast)
measured From Day 1 (Treatment Period 1) to Day 13 (end of Treatment Period 2)
Part B: Area under concentration-time curve from time 0 to infinity (AUCinf)
measured From Day 1 (Treatment Period 1) to Day 13 (end of Treatment Period 2)
Part B: Time to reach maximum observed concentration (tmax)
measured From Day 1 (Treatment Period 1) to Day 13 (end of Treatment Period 2)

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