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A Study to Assess Change in Disease Activity, Adverse Events, and How the Drug Moves Through the Body in Adult Participants Living With Human Immunodeficiency Virus (HIV) Receiving Intravenous (IV) Infusion or Subcutaneous (SC) Injection of Budigalimab and/or ABBV-382

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NCT06032546

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

Phase
Phase 2
Status
Terminated
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
163actual
Sites
80
Countries
Belgium, Brazil, Canada +10

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

Why the sponsor stopped it

Company Decision

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-10-12actualWhen the study began enrolling
Primary completion2025-09-22actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-09-22actualThe whole study's end, after follow-up
First posted2023-09-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Human Immuno-deficiency Virus (HIV) Disease

Interventions

  • Drug: Budigalimab — also filed as ABBV-181
  • Drug: Placebo for Budigalimab
  • Drug: ABBV-382
  • Drug: Placebo for ABBV-382
  • Drug: Budigalimab — also filed as ABBV-181

Primary outcomes

what the primary-completion date above is the date OF
Percentage of Participants with Viral Control Without Antiretroviral Therapy (ART) Restart
measured Week 24
Number of Participants with Adverse Events (AEs)
measured Up to approximately Week 112

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