A Phase 1 Study to Assess the Effect of Itraconazole on ABBV-722 in Healthy Adult Participants
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Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Na · 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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-05-05 | estimated | When the study began enrolling |
| Primary completion | Jul 2026 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | Jul 2026 | estimated | The whole study's end, after follow-up |
| First posted | 2026-05-20 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-05-20 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Healthy Volunteers
Interventions
- Drug: ABBV-722
- Drug: Itraconazole
Primary outcomes
what the primary-completion date above is the date OFMaximum Observed Plasma Concentration (Cmax) of ABBV-722
measured Up to Day 8 in Period 1 and Up to Day 14 in Period 2
Time to Cmax (Tmax) of ABBV-722
measured Up to Day 8 in Period 1 and Up to Day 14 in Period 2
Area Under the Plasma Concentration-Time Curve From Time 0 to Time of Last Measurable Concentration (AUCt) of ABBV-722
measured Up to Day 8 in Period 1 and Up to Day 14 in Period 2
Area Under the Plasma Concentration-Time Curve From Time 0 to Infinite Time (AUCinf) of ABBV-722
measured Up to Day 8 in Period 1 and Up to Day 14 in Period 2
Terminal Phase Elimination Rate Constant (β) of ABBV-722
measured Up to Day 8 in Period 1 and Up to Day 14 in Period 2
Terminal Phase Elimination Half-Life (t1/2) of ABBV-722
measured Up to Day 8 in Period 1 and Up to Day 14 in Period 2
Number of Participants with Adverse Events (AEs)
measured Up to Approximately 45 Days
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