RecruitingPhase 1NCT07556484

Pharmacokinetics Of Emulsified Avacopan Applied By NG Tube

Pharmacokinetics Of Emulsified Avacopan In ANCA-associated Vasculitis With Severe Diffuse Alveolar Hemorrhage


Sponsor

Mayo Clinic

Enrollment

6 participants

Start Date

May 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to determine the 72-hour pharmacokinetics of emulsified avacopan at a dose of 30 mg twice daily given to up to 6 patients with active severe GPA or MPA with diffuse alveolar hemorrhage (DAH) requiring mechanical ventilation for respiratory support.


Eligibility

Min Age: 18 Years

Inclusion Criteria7

  • Fulfillment of the definitions of the Second Chapel Hill Consensus Conference for ANCA-associated vasculitis (either granulomatosis with polyangiitis (GPA) or microscopic polyangiitis MPA).
  • Positivity for ANCA, directed against PR3 or MPO.
  • Diffuse alveolar hemorrhage.
  • Respiratory failure requiring mechanical ventilation.
  • Severe newly diagnosed disease or severe relapsing disease. Severe new or relapsing disease is defined as at least one major BVAS/WG item or a score ≥ 3 and the investigator deems standard treatment for severe disease is necessary.
  • Minimum BVAS-WG of 3.
  • Requirement of standard-of-care remission induction therapy for active severe ANCA-associated vasculitis (GPA or MPA).

Exclusion Criteria9

  • Diagnosis with eosinophilic granulomatosis with polyangiitis (EGPA, formally Churg-Strauss syndrome) as defined by the Chapel Hill consensus conference.
  • Allergies: History of severe allergic reaction to avacopan
  • History of documented anti-glomerular basement membrane disease (anti-GBM disease)
  • Previous administration of avacopan within the last 5 days.
  • Concomitant use of a strong CYP3A4 inhibitor.
  • Aspartate aminotransferase \[AST\], alanine amino transferase \[ALT\], alkaline phosphatase, or total bilirubin elevation >2.5 times the upper limit of normal (unless attributed to vasculitis) on routine liver function testing obtained within 3 days prior to anticipated treatment with avacopan.
  • Evidence of prior active or current Hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency (HIV) infection.
  • Active serious infection, including localized infection.
  • Pregnancy and breastfeeding

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Interventions

DRUGAvacopan

Avacopan capsules will be solubilized in heated water and administered to patients with Diffuse Alveolar Hemorrhage (DAH) due to GPA or MPA via nasogatric tube.


Locations(1)

Mayo Clinic in Rochester

Rochester, Minnesota, United States

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NCT07556484


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