Interleukin-4Ra Blockade by Dupilumab Decreases Staphylococcus Colonization and Increases
Hypothesis: The investigators hypothesize that in patients with CRSwNP who demonstrate sinus colonization with staphylococcus aureus, the administration of dupilumab will be associated with decreased staph colonization and an increase in microbial diversity. Primary Objective will be to demonstrate that dupilumab reduc
| Condition(s) | Nasal Polyps, Staphylococcus Aureus |
|---|---|
| Status | Recruiting |
| Phase | Phase 4 |
| Study type | Interventional |
| Summary | Hypothesis: The investigators hypothesize that in patients with CRSwNP who demonstrate sinus colonization with staphylococcus aureus, the administration of dupilumab will be associated with decreased staph colonization and an increase in microbial diversity. Primary Objective will be to demonstrate that dupilumab reduces staphylococcus aureus (phyla firmicutes) abundance while increasing microbial diversity in patients with CRSwNPs who are culture positive for staph aureus at enrollment. Secondary Objectives will be to correlate reduction in Staph aureus abundance and improved bacterial diversity with increased expression of anti-microbial proteins (ß-defensins1-4) and cathelicidin LL-37. In addition, the investigators will correlate improvements in microbial diversity/decreased staph abun |
| Who can participate | Inclusion Criteria: • Adults, ages 18-65 * History of CRSwNP including subjects with AERD * Sinonasal culture demonstrating staph aureus at visit 1 * History of FESS with patent sinus ostia sufficient to obtain culture and tissue samples from the middle meatus * Asthma, if present, should be well controlled * Atopic dermatitis, if present, should be well controlled * Use of nasal saline irrigation and stable dosing (\>1 month) of topical corticosteroids is permitted * Intent of the physicians caring to start dupilumab therapy as part of subject's standard of care * Subject meets FDA approved criteria for the use of dupilumab for nasal polyps Exclusion Criteria: * Concurrent serious medical problem * Uncontrolled asthma (ACT \<20 at screening visit) * Recent (within 60 days) use of oral cor |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Lead sponsor | University of Virginia |
| Locations | Charlottesville, Virginia, United States |
| Start date | 2022-09-01 |
| NCT ID | NCT05094570 |
| Official listing | https://clinicaltrials.gov/study/NCT05094570 |