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A Study to Evaluate How Multiple Doses of Itraconazole Interacts With Nacresertib in Healthy Adult Participants

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NCT07649954 · readout ≤ 42 d

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Basic science
Enrollment
12estimated
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
Start2026-06-23actualWhen the study began enrolling
Primary completionSep 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionSep 2026estimatedThe whole study's end, after follow-up
First posted2026-06-16actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-23actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Volunteer

Interventions

  • Drug: Nacresertib
  • Drug: Itraconazole

Primary outcomes

what the primary-completion date above is the date OF
Maximum Observed Plasma Concentration (Cmax) of Nacresertib
measured Up to Day 12
Time to Cmax (Tmax) of Nacresertib
measured Up to Day 12
Area Under the Plasma Concentration-Time Curve (AUC) From Time 0 to the Time of the Last Measurable Concentration (AUCt) of Nacresertib
measured Up to Day 12
AUC From Time 0 to the Time Infinity (AUCinf) of Nacresertib
measured Up to Day 12
Terminal Phase Elimination Rate Constant (Beta) of Nacresertib
measured Up to Day 12
Terminal Phase Elimination Half-Life (t1/2) of Nacresertib
measured Up to Day 12

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