Phase
Condition
Sinusitis
Soft Tissue Infections
Nasal Obstruction
Treatment
dupilumab
placebo
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age 18-75 with history of chronic sinusitis without polyps
SNOT-22 score of at least 30 at baseline
Bilateral Lund-Mackay CT score 4 or more and/or MLK endoscopy score 4 or more
Blood eosinophil count of at least 300/ul and/or SPT positive to at least 5/30allergens, or eosinophil less than 300/ul and SPT negative (Th2 low group).
Prior oral steroid or antibiotic use is acceptable but not required for entry
Informed Consent
Effective birth control (with <1% failure rate), post menopausal or documentedabstinence
Women ≥50 years old would be considered postmenopausal if they have been amenorrheicfor 12 months or more following cessation of all exogenous hormonal treatment.
All male subjects who are sexually active must agree to use an acceptable method ofcontraception (condom or vasectomy) from V1-V16
Exclusion
Exclusion Criteria:
Immunosuppression other than oral steroids in the past 3 months
History of nasal polyps within the past 3 years or noted at screening by CT orendoscopy
Acute sinusitis at the time of entry
Acute fungal sinusitis at the time of entry
Uncontrolled asthma
Cystic fibrosis
Primary immune deficiency including CVID
Other; serious concomitant illness or sinus disease that the investigator determinesto disqualify
A history of known immunodeficiency disorder including HIV
History of hepatitis B or C
Primary ciliary dyskinesia (PCD)
Use of any biologic medication within the last 5 months or 5 half-lives whichever islonger
Receipt of any investigational non-biologic within 5 half-lives prior to visit 0
Receipt of immunoglobulin or blood products within 30 days prior to V1
Scheduled sinus surgery
Significant structural abnormalities or severe septal deviation
Symptomatic or untreated life threatening cardiopulmonary disorders
History of cancer not in remission at least 5 years prior to the date informedconsent
Subjects who are febrile (≥38°C; ≥100.4°F);
Untreated helminth parasitic infection within 24 weeks prior to informed consent
Pregnant or nursing
Any other medical illness that precludes study involvement
History of anaphylaxis to any biologic therapy or vaccine
The following medications are excluded:
Any type of anti-interleukin therapy (e.g. Omalizumab, benralizumab, dupilumabmepolizumab, reslizumab, lebrikizumab etc.) within the last 5 months or 5half-lives whichever is longer
Receipt of any investigational non-biologic within 30 days or 5 half-livesprior to visit 0, whichever is longer.
Immunosuppressive medications such as methotrexate, azathioprine, cyclosporine,tacrolimus
Receipt of immunoglobulin or blood products within 30 days prior to the dateinformed consent is obtained.
Daily high dose aspirin greater than 81mg daily
Allergen Immunotherapy during build-up phase during the last three months
Other medications that could interfere with the action of dupilumab or suppresseosinophils
Study Design
Study Description
Connect with a study center
Johns Hopkins University School of Medicine
Baltimore, Maryland 21224
United StatesSite Not Available
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