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A Study to Assess the Adverse Events and How Subcutaneous (SC) Injections and Intravenous (IV) Infusions of ABBV-142 Move Through the Body of Healthy Adult Participants

← catalyst calendar

NCT06774313

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · Quadruple · Basic science
Enrollment
73actual
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
Start2025-01-22actualWhen the study began enrolling
Primary completion2026-04-08actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-04-08actualThe whole study's end, after follow-up
First posted2025-01-14actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-06actualThe 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: ABBV-142
  • Drug: ABBV-142
  • Drug: Placebo
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants with Adverse Events (AEs)
measured Up to Day 120
Maximum Observed Serum Concentration (Cmax) of ABBV-142
measured Up to Day 120
Time to Cmax (Tmax) of ABBV-142
measured Up to Day 120
Area Under the Serum Concentration-time Curve (AUC) of ABBV-142 from Time 0 to the Time of Last Measurable Concentration (AUCt)
measured Up to Day 120
AUC of ABBV-142 from Time 0 to Infinity (AUCinf)
measured Up to Day 120
Terminal Phase Elimination Rate Constant (β) of ABBV-142
measured Up to Day 120
Terminal Phase Elimination Half-life (t1/2) of ABBV-142
measured Up to Day 120
Dose Normalized Cmax of ABBV-142
measured Up to Day 120
Dose Normalized AUC of ABBV-142
measured Up to Day 120

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