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A Study to Investigate the Effect of Capivasertib on the Pharmacokinetics of Oral Dextromethorphan (CYP2D6 Substrate) in Healthy Participants

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NCT07241065

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Na · None · Other
Enrollment
42actual
Sites
1
Country
Germany

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
Start2026-03-19actualWhen the study began enrolling
Primary completion2026-07-20actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-07-20actualThe whole study's end, after follow-up
First posted2025-11-21actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-27actualThe 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: Dextromethorphan
  • Drug: Capivasertib

Primary outcomes

what the primary-completion date above is the date OF
Area under concentration time curve from time 0 to infinity (AUCinf) of dextromethorphan
measured Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8
Area under concentration curve from time 0 to the last quantifiable concentration (AUClast) of dextromethorphan
measured Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8
Maximum observed drug concentration (Cmax) of dextromethorphan
measured Period 1: Day 1 to Day 3, Period 2: Day 6 to Day 8

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