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A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-981) in Adult Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-Tumor Necrosis Factor (TNF) Therapy and Who Are Naïve to Biologic Therapy

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NCT05139602 · readout ≤ 499 d

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

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
210actual
Sites
54
Countries
Australia, Canada, Germany +5

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
Start2021-12-28actualWhen the study began enrolling
Primary completionDec 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2027estimatedThe whole study's end, after follow-up
First posted2021-12-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Hidradenitis Suppurativa

Interventions

  • Biological: Lutikizumab — also filed as ABT-981
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Percentage of Participants Achieving Hidradenitis Suppurative Clinical Response (HiSCR)
measured Week 16
Number of Participants with Adverse Events (AEs)
measured Up to Approximately Week 68

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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