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A Study to Assess How the Body Absorbs ABBV-8736 Subcutaneous Injections Relative to Intravenous Injections in Adult Healthy Volunteers

← catalyst calendar

NCT07413133

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
40actual
Sites
2
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
Start2026-02-11actualWhen the study began enrolling
Primary completion2026-06-19actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-06-19actualThe whole study's end, after follow-up
First posted2026-02-17actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-20actualThe 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-8736
  • Drug: ABBV-8736

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants with Adverse Events (AEs)
measured Up to At Least 3 Months
Maximum Observed Serum Concentration (Cmax) of ABBV-8736
measured Up to At Least 3 Months
Time to Maximum Observed Serum Concentration (Tmax) of ABBV-8736
measured Up to At Least 3 Months
Area Under the Plasma Concentration-Time Curve (AUC) From Time 0 to the Time Last (AUClast) of ABBV-8736
measured Up to At Least 3 Months
AUC From Time 0 to the Time Infinity (AUCinf) of ABBV-8736
measured Up to At Least 3 Months
Terminal Phase Elimination Rate Constant (β) of ABBV-8736
measured Up to At Least 3 Months
Terminal Elimination Half-Life (t1/2) of ABBV-8736
measured Up to At Least 3 Months
Apparent Clearance of the Analyte in Serum (CL) of ABBV-8736
measured Up to At Least 3 Months

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