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

AbbVie

Status and phase: Active, not recruiting; Phase 2

Conditions: Hidradenitis Suppurativa

Treatments: Drug: Placebo; Biological: Lutikizumab

Study type: Interventional

Funder types: Industry

Identifiers

NCT05139602

M20-262

2020-004108-33 (EudraCT Number)

Details and patient eligibility

About

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 treatment of HS. In the Main Study, participants will be put in 1 of 4 groups, called treatment arms. There is a 1 in 4 chance that participants will be assigned to placebo. Around 160 adult participants with moderate to severe HS who have failed anti-TNF therapy will be enrolled in the study at approximately 50 sites worldwide. In the Sub-study, participants will be put in 1 of 2 groups, called treatment arms. Both arms will receive treatment at different dosing intervals. Around 40 adult participants with moderate to severe HS who are naïve to biologic therapy will be enrolled in the study at certain sites.

In the Main Study, participants will receive subcutaneous injections of lutikizumab (ABT-981) or placebo every week for 16 weeks. In the Sub-study, participants will receive subcutaneous injections of lutikizumab (ABT-981) every week for the first 15 weeks, then either every week or every other week for 36 weeks.

There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires and diaries.

Enrollment: 210 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• A clinical diagnosis of hidradenitis suppurativa (HS) for at least 1 year prior to Baseline as determined by the investigator.
• A total abscess and inflammatory nodule (AN) count of >= 5 at Baseline
• HS lesions must be present in at least 2 distinct anatomic areas.
• Must have failed anti-TNF treatment for HS.
• To be eligible for the Sub-study, participants must be naïve to biologic therapy for treatment of HS.

Exclusion criteria

• History of active skin disease other than HS that could interfere with the assessment of HS, including skin infections (e.g., bacterial, fungal, or viral) requiring systemic treatment within 4 weeks of the Baseline visit.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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210 participants in 6 patient groups, including a placebo group

Main Study: Lutikizumab Dose A

Experimental group

Description:

Lutikizumab Dose A every week

Treatment:

Biological: Lutikizumab

Main Study: Lutikizumab Dose B

Experimental group

Description:

Lutikizumab Dose B every other week

Treatment:

Biological: Lutikizumab

Main Study: Lutikizumab Dose C

Experimental group

Description:

Lutikizumab Dose C every other week

Treatment:

Biological: Lutikizumab

Main Study: Placebo

Placebo Comparator group

Description:

Placebo every week

Treatment:

Drug: Placebo

Sub-study: Group 1

Experimental group

Description:

Period 1: Lutikizumab Dose A every week. Period 2: Lutikizumab Dose A every week.

Treatment:

Biological: Lutikizumab

Sub-study: Group 2

Experimental group

Description:

Period 1: Lutikizumab Dose A every week. Period 2: Lutikizumab Dose A every other week.

Treatment:

Biological: Lutikizumab