Efficacy and Safety Study of Benralizumab for Patients with Severe Nasal Polyposis - OSTRO

Exclusion Criteria

• 1. Patients who have undergone any nasal and/or sinus surgery within 3 months prior to V1.
• 2. Patients with conditions or concomitant disease that makes them non evaluable for the co-primary efficacy endpoint such as:
• - Unilateral antrochoanal polyps;
• - Nasal septal deviation that occludes at least one nostril;
• - Acute sinusitis, nasal infection, or upper respiratory infection at screening or in the 2 weeks before screening;
• - Current rhinitis medicamentosa;
• - Allergic fungal rhinosinusitis (AFRS) or Allergic fungal sinusitis (AFS);
• - Nasal cavity tumors.
• 3. Clinically important comorbidities that could confound interpretation of clinical efficacy results including, but not limited to: active upper or lower respiratory tract infection, cystic fibrosis, primary ciliary dyskinesia, eosinophilic diseases other than asthma (e.g. allergic bronchopulmonary aspergillosis/mycosis, eosinophilic granulomatosis with polyangitis [Churg-Strauss syndrome], hypereosinophilic syndromes), granulomatosis with polyangitis (Wegener's granulomatosis), Young’s syndrome, etc.
• 4. Any disorder, including but not limited to: cardiovascular, gastrointestinal, hepatic, renal, neurological, musculoskeletal, infectious, endocrine, metabolic, haematological, psychiatric, or major physical impairment that is not stable in the opinion of the Investigator or AstraZeneca and could:
• - Affect the safety of the patient throughout the study;
• - Influence the findings of the studies or their interpretations;
• - Impede the patient’s ability to complete the entire duration of study.
• 5. Patients experiencing an asthma exacerbation requiring systemic (oral and/or parenteral) corticosteroids treatment or hospitalization (>24hrs) for treatment of asthma within 4 weeks prior to V1.
• 6. History of anaphylaxis to any biologic therapy or vaccine.
• 7. Known history of allergy or reaction to any component of the Investigational Product (IP) formulation.
• 8. History of Guillain-Barré syndrome.
• 9. A helminth parasitic infection diagnosed within 24 weeks prior to V1 and has not been treated with, or has failed to respond to standard of care therapy.
• 10. Current malignancy, or history of malignancy, except for: - Patients who have had basal cell carcinoma, localized squamous cell carcinoma of the skin, or in situ carcinoma of the cervix are eligible provided that patient is in remission and curative therapy was completed at least 12 months prior to V1; - Patients who have had other malignancies are eligible provided that the patient is in remission and curative therapy was completed at least 5 years prior to V1.
• NOTE: Hormonal therapy is allowed. As long as the cancer is in remission for 5 years, the patient is eligible.
• 11. Any clinically significant cardiac disease or any electrocardiogram (ECG) abnormality obtained during the screening/run-in period, which may put the patient at risk or interfere with study assessments.
• 12. Positive hepatitis B surface antigen, or hepatitis C virus antibody serology (confirmed by additional testing, e.g. hepatitis C RNA test, if indicated), or a positive medical history for hepatitis B or C (Note: Patients with history of hepatitis B vaccination without history of hepatitis B are allowed to enroll).
• 13. History of known immunodeficiency disorder, including a positive human immunodeficiency virus (HIV) test.
• 14. Infection requiring systemic antibiotics (Ab) within 14 days prior to V1
• 15. Use of immunosuppressive medication (including but not limited to: methotrexate, troleandomycin, cyclosporine, azathioprine, or any experimental anti-inflammatory therapy) within 3 months prior to V1.
• 16. Receipt of any marketed or investigational biologic products (monoclonal or polyclonal antibody) within 6 months or 5 half-lives prior to the date informed consent, is obtained, whichever is longer, prior to V1 and during the study period. This also applies to patients who previously participated in clinical studies and were treated with monoclonal antibodies (e.g. mepolizumab, reslizumab, dupilumab, omalizumab). Note that this restriction do not apply to patients, who are confirmed to have only received treatment with placebo.
• 17. Previous receipt of benralizumab.
• 18. Receipt of immunoglobulin or blood products within 30 days prior to V1.
• 19. Receipt of live attenuated vaccines 30 days prior to the date of randomization.
• 20. Receipt of any investigational drug within 30 days or 5 half-lives whichever is longer prior to randomization.
• 21. Receipt of systemic corticosteroid 4 weeks prior to V1, or a scheduled systemic corticosteroid treatment during the study period.
• NOTE: Sustained release steroids (e.g. Kenalog [Triamcinolone acetonide]) or depot injections require minimum 6 weeks washout prior to V1.
• 22. Receipt of leukotriene antagonist/modifiers for patients who were not on a continuous stable dose for ≥30 days prior to V1.
• 23. Concurrent enrolment in another clinical drug interventional trial.
• 24. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) level ≥ 3 times the upper limit of normal (ULN) confirmed during screening period.
• 25. Previous randomization in the present study.
• 26. Planned major surgical procedures or scheduled NP surgery at the time of the study enrolment and randomization.
• 27. Initiated or is being maintained on an aspirin desensitization regimen for the management of aspirin exacerbated respiratory disease (AERD) at the time of study enrolment or during the run-in period.
• 28. For women only – currently pregnant (or intend to become pregnant), breastfeeding or lactating.