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NCT07556484RecruitingPhase 1

Pharmacokinetics Of Emulsified Avacopan Applied By NG Tube

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

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
6 (estimated)
First submitted
8 Apr 2026
Start date
1 Aug 2027
Primary completion date
1 Aug 2028
Lead sponsor
Mayo Clinic
NCT number
NCT07556484

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 6
  • From 1 Aug 2027 to the primary completion date, 1 Aug 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous administration of avacopan within the last 5 days.
  • Concomitant use of a strong CYP3A4 inhibitor.
  • Evidence of prior active or current Hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency (HIV) infection.

Other illness

  • 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)
  • Active serious infection, including localized infection.

Lab values

  • 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.

Other

  • Pregnancy and breastfeeding

Who the study is looking for

  • 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).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.