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A Study of Absorption, Distribution, Metabolism and Excretion (ADME) of [14C]AZD4144

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NCT07518459

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
16actual
Sites
1
Country
United Kingdom

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
Start2026-02-11actualWhen the study began enrolling
Primary completion2026-05-26actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-05-26actualThe whole study's end, after follow-up
First posted2026-04-08actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-22actualThe 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: [14C]AZD4144 Solution for Infusion — also filed as AZD4144
  • Drug: [14C]AZD4144 Oral Solution — also filed as AZD4144

Primary outcomes

what the primary-completion date above is the date OF
Amount of AZD4144 excreted (Ae)
measured Urine and faecal samples collected from pre-dose until up to 216 hours post-dose
Amount of AZD4144 excreted expressed as a percentage of the radioactive dose administered (Fe)
measured Urine and faecal samples collected from pre-dose until up to 216 hours post-dose
Cumulative amount of AZD4144 excreted (CumAe)
measured Urine and faecal samples collected from pre-dose until up to 216 hours post-dose
Cumulative amount of AZD4144 excreted expressed as a percentage of the radioactive dose administered (CumFe)
measured Urine and faecal samples collected from pre-dose until up to 216 hours post-dose
Area under the curve (AUC) of circulating plasma total radioactivity (TR) accounting for 10% or more of the dose
measured Plasma, urine and faecal samples from pre-dose until up to 216 hours post-dose
80% or more of the radioactivity recovered in excreta
measured Plasma, urine and faecal samples from pre-dose until up to 216 hours post-dose

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