Overview

The primary purpose of the study is evaluate the effect of brensocatib compared with placebo.

Eligibility

Inclusion Criteria:

• Diagnosis of HS (confirmed by a dermatologist), with a history of signs and symptoms consistent with HS for at least 6 months before the Screening Visit.
• Moderate or severe HS defined as a total of ≥6 inflammatory lesions (inflammatory nodules and/or abscesses) for at least 8 weeks before the Baseline Visit.
• HS lesions in at least 2 distinct anatomic areas, 1 of which must be at least Hurley Stage II or Hurley Stage III at both the Screening and Baseline Visits.

Exclusion Criteria:

• Draining tunnel count of ≥20 at the Baseline Visit.
• Surgical or laser intervention for an HS lesion during the Screening Period.
• Clinical diagnosis of Papillon-Lefèvre Syndrome.
• Participants with an absolute neutrophil count <1,000/mm3 at the Screening Visit.
• Participants having active liver disease or hepatic dysfunction.
• Have diagnosed periodontal disease under active management by a dentist or expected to have periodontal disease-related procedures within the study period.
• Received systemic (intravenous or orally [PO]) antibiotic therapy within 8 weeks before the Baseline Visit
  1. Doxycycline or minocycline up to 100 mg twice daily is permitted provided the dosing regimen being stable for at least 8 weeks before the Baseline Visit and is expected to continue.
• Received PO or transdermal opioid analgesics (except tramadol) for any reason within

  4 weeks before the Baseline Visit.

• Permitted analgesics for HS-related pain have not been at a stable dose regimen for at least 4 weeks before the Baseline Visit.
• Received prescription topical therapies for the treatment of HS within 2 weeks before the Baseline Visit.
• Received any anti-tumor necrosis factor (TNF)-α/other biologics treatment within 12 weeks or 5 elimination half-lives, whichever is longer, before the Baseline Visit.
• Received systemic nonbiologic therapies (eg, corticosteroids and retinoids) for HS within 4 weeks before the Baseline Visit.
• Received any immunomodulatory agents within 4 weeks before the Baseline Visit.

Note: Other Inclusion/Exclusion criteria may apply.