Dupilumab Treatment Effects in an Ethnically Diverse Population With Chronic Rhinosinusitis With Nasal Polyposis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorMontefiore Medical Center

About this trial

The central hypothesis of this study is that the addition of dupilumab treatment onto standard-of-care intranasal corticosteroids will improve patient-reported measures of disease activity and sense of smell in a cohort of mostly ethnical and racial minority patients with CRSwNP

Eligibility criteria

Qualifiers

Patients with physician-diagnosed CRSwNP, with or without comorbid asthma that meet indication criteria for FDA-approved use of Dupilumab.

Patients aged 18 years and older.

Patient willing to provide consent to be a participant in the study.

Patients with insurance that allows Dupilumab coverage or Dupilumab coverage obtained through "Dupixent MyWay Program"

Disqualifiers

Age under 18

Suspected or diagnosed allergic fungal rhinosinusitis.

Suspected or diagnosed cystic fibrosis.

Dupilumab coverage denied through insurance or "Dupixent MyWay Program"

Trial design

Treatments tested in this trial

  • Dupilumab

Treatment groups

60 Participants
are divided into 1 treatment group

Sponsors and collaborators

Montefiore Medical Center

Lead sponsor

Regeneron Pharmaceuticals

Collaborator

Mayo Clinic

Collaborator