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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

Active, not recruiting · Phase 2 · NCT05139602

Conditions: Hidradenitis Suppurativa

At a glance

Research payments reported, 2025
$316,732
U.S. investigators named
16
Sites paid
17
Planned or actual enrollment
210

About the trial

Sponsor
AbbVie
Tested
Lutikizumab (biological), Placebo (drug)
Dates
Started 2021-12-28; completion 2027-12
Results posted
Not yet

Hidradenitis suppurativa (HS) is a chronic and often painful inflammatory skin disease which includes the forming of lumps, abscesses and scars in areas of the skin such as under the breasts, under armpits, inner thighs, groin and buttocks. Despite the clinical benefit anti-tumor necrosis factor (TNF) therapy offers to patients with HS, there remains a significant unmet medical need for patients who fail to achieve adequate benefit with anti-TNF therapy. This study will compare lutikizumab (ABT-981) versus placebo for the treatment of adult participants with moderate to severe HS who have failed anti-TNF therapy. Lutikizumab (ABT-981) is an investigational drug being developed for the tre…

From ClinicalTrials.gov, last updated 2026-02-13. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $316,732 in research payments for this study in 2025 (159 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.