Efficacy and Safety Study of Benralizumab in Patient With Eosinophilic Chronic Rhinosinusitis With Nasal Polyps (ORCHID) (ORCHID)
Primary Purpose
Nasal Polyposis
Status
Active
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Benralizumab 30 mg
Matched placebo
Sponsored by
About this trial
This is an interventional treatment trial for Nasal Polyposis focused on measuring Benralizumab, Nasal Polyposis, Eosinophilic Chronic Rhinosinusitis with Nasal Polyposis, Nasal Polyps, Asthma
Eligibility Criteria
Inclusion criteria:
- Female or male patients aged 18 to 75 years inclusive
- Stable Intranasal corticosteroids (INCS) use for at least 4 weeks prior to enrolment and throughout screening
- History of treatment with systemic corticosteroids (SCS) or prior surgery for CRSwNP
- Bilateral sinonasal polyposis with a nasal polyp score (NPS) of 5 at enrolment and randomization (unilateral score of at least 2 for each nostril)
- Ongoing symptoms for at least 12 weeks prior to enrolment
- Patient-reported moderate to severe nasal blockage score (NBS) ≥2 at enrolment
- Bi-weekly mean NBS ≥ 1.5 at randomization
- SNOT-22 total score ≥ 20 at enrolment and randomization
- Documented physician-diagnosed asthma
- Blood eosinophil count of >2% or ≥150/μL at enrolment
Exclusion criteria:
- Any nasal and/or sinus surgery within 3 months prior to enrolment
Patients with conditions that makes them non evaluable for the co-primary efficacy endpoint including but not limited to:
- Unilateral antrochoanal polyps
- Nasal septal deviation that occludes at least one nostril
- Current rhinitis medicamentosa
- Allergic fungal rhinosinusitis or allergic fungal sinusitis;
- Clinically important comorbidities that may put the patient at risk, or may confound interpretation of clinical efficacy and/or safety results
- Receipt of SCS for within 4 weeks prior to screening, or a scheduled SCS treatment during the study period.
- Receipt of any marketed or investigational biologic product within 6 months of enrolment
- Currently pregnant or breastfeeding
Sites / Locations
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Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Benralizumab
Placebo
Arm Description
Benralizumab administered subcutaneously
Placebo administered subcutaneously
Outcomes
Primary Outcome Measures
Nasal Polyp Burden
Change from baseline in endoscopic total nasal polyp score (NPS).
Patient-reported Nasal Blockage (NB)
Change from baseline in mean nasal blockage score (NBS).
Secondary Outcome Measures
Sense of Smell
Change from baseline in difficulty with sense of smell (DSS) score
Sinus Opacification by CT Scan
Change from baseline in Lund Mackay score
Disease specific health-related quality of life (HRQoL)
Change from baseline in SinoNasal Outcome Test (SNOT-22) score.
Nasal Polyp Surgery
Time to first nasal polyp surgery
Systemic corticosteroid (SCS) use
Time to first SCS course for NP
Symptoms associated with CRSwNP
Change from baseline in nasal symptom score(s)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04157335
Brief Title
Efficacy and Safety Study of Benralizumab in Patient With Eosinophilic Chronic Rhinosinusitis With Nasal Polyps (ORCHID)
Acronym
ORCHID
Official Title
A Multicentre, Randomised, Double-Blind, Parallel-Group, Placebo-Controlled Phase 3 Efficacy and Safety Study of Benralizumab in Patients With Eosinophilic Chronic Rhinosinusitis With Nasal Polyps (ORCHID)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 25, 2019 (Actual)
Primary Completion Date
August 19, 2024 (Anticipated)
Study Completion Date
October 10, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AstraZeneca
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomized, double-blind, placebo-controlled, parallel-group, international, multicenter, Phase 3 study to evaluate the efficacy and safety of repeat dosing of benralizumab 30 mg administered subcutaneously (SC) versus placebo in patients with severe nasal polyposis.
Detailed Description
Approximately 275 patients will be randomized to receive benralizumab 30 mg SC or matching placebo. After enrolment, eligible patients will enter a 6-week screening/run in period. Patients who meet eligibility criteria will be randomised 1:1 at Week 0 (Day 0) to receive either placebo or benralizumab 30 mg SC every 4 weeks for the first 3 doses (Weeks 0, 4 and 8) and every 8 weeks thereafter (Weeks 16, 24, 32, 40 and 48). An end of treatment visit will be conducted at Week 56.All patients who complete the 56-week DB treatment period on investigational product (IP) may be eligible to continue into around one year OLE, during which all patients will receive 8 doses of benralizumab 30 mg. Patients in Benra arm during DB period will receive one dummy dose. The last study visit will occur at 8 weeks after the last dose of IP (Week 112/FU). Patients who do not enter OLE, will have their last study visit at Week 56 (EoDB) for follow-up and without administration of IP.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasal Polyposis
Keywords
Benralizumab, Nasal Polyposis, Eosinophilic Chronic Rhinosinusitis with Nasal Polyposis, Nasal Polyps, Asthma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
295 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Benralizumab
Arm Type
Experimental
Arm Description
Benralizumab administered subcutaneously
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo administered subcutaneously
Intervention Type
Biological
Intervention Name(s)
Benralizumab 30 mg
Intervention Description
Benralizumab is 30 mg/ml solution for injection in accessorized pre-filled syringe, 1 ml fill volume.
Benralizumab 30 mg subcutaneously will be injected every 4 weeks for the first 3 doses (Weeks 0, 4 and 8) and every 8 weeks thereafter (Weeks 16, 24, 32, 40 and 48).
Intervention Type
Biological
Intervention Name(s)
Matched placebo
Intervention Description
Matching placebo solution for injection in accessorized pre-filled syringe. 1 ml fill volume.
Matching placebo subcutaneously will be injected every 4 weeks for the first 3 doses (Weeks 0, 4 and 8) and every 8 weeks thereafter (Weeks 16, 24, 32, 40 and 48).
Primary Outcome Measure Information:
Title
Nasal Polyp Burden
Description
Change from baseline in endoscopic total nasal polyp score (NPS).
Time Frame
Baseline and Week 56
Title
Patient-reported Nasal Blockage (NB)
Description
Change from baseline in mean nasal blockage score (NBS).
Time Frame
Baseline and week 56
Secondary Outcome Measure Information:
Title
Sense of Smell
Description
Change from baseline in difficulty with sense of smell (DSS) score
Time Frame
Week 56
Title
Sinus Opacification by CT Scan
Description
Change from baseline in Lund Mackay score
Time Frame
Week 56
Title
Disease specific health-related quality of life (HRQoL)
Description
Change from baseline in SinoNasal Outcome Test (SNOT-22) score.
Time Frame
Week 56
Title
Nasal Polyp Surgery
Description
Time to first nasal polyp surgery
Time Frame
Week 56
Title
Systemic corticosteroid (SCS) use
Description
Time to first SCS course for NP
Time Frame
Week 56
Title
Symptoms associated with CRSwNP
Description
Change from baseline in nasal symptom score(s)
Time Frame
Week 56
Other Pre-specified Outcome Measures:
Title
Assessment the safety and tolerability of benralizumab
Description
AEs, Vital signs, Clinical Laboratory and ECG
Time Frame
Week 56
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Female or male patients aged 18 to 75 years inclusive
Stable Intranasal corticosteroids (INCS) use for at least 4 weeks prior to enrolment and throughout screening
History of treatment with systemic corticosteroids (SCS) or prior surgery for CRSwNP
Bilateral sinonasal polyposis with a nasal polyp score (NPS) of 5 at enrolment and randomization (unilateral score of at least 2 for each nostril)
Ongoing symptoms for at least 12 weeks prior to enrolment
Patient-reported moderate to severe nasal blockage score (NBS) ≥2 at enrolment
Bi-weekly mean NBS ≥ 1.5 at randomization
SNOT-22 total score ≥ 20 at enrolment and randomization
Documented physician-diagnosed asthma
Blood eosinophil count of >2% or ≥150/μL at enrolment
Exclusion criteria:
Any nasal and/or sinus surgery within 3 months prior to enrolment
Patients with conditions that makes them non evaluable for the co-primary efficacy endpoint including but not limited to:
Unilateral antrochoanal polyps
Nasal septal deviation that occludes at least one nostril
Current rhinitis medicamentosa
Allergic fungal rhinosinusitis or allergic fungal sinusitis;
Clinically important comorbidities that may put the patient at risk, or may confound interpretation of clinical efficacy and/or safety results
Receipt of SCS for within 4 weeks prior to screening, or a scheduled SCS treatment during the study period.
Receipt of any marketed or investigational biologic product within 6 months of enrolment
Currently pregnant or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luo Zhang, Prof. Dr.
Organizational Affiliation
Beijing Tongren Hospital
Official's Role
Principal Investigator
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Turkey
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Hanoi
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Vietnam
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12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
IPD Sharing Time Frame
AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
IPD Sharing Access Criteria
When a request has been approved AstraZeneca will provide access to the de-identified individual patient-level data in an approved sponsored tool . Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
IPD Sharing URL
https://astrazenecagroup-dt.pharmacm.com/DT/Home
Citations:
PubMed Identifier
33710614
Citation
Chong LY, Piromchai P, Sharp S, Snidvongs K, Webster KE, Philpott C, Hopkins C, Burton MJ. Biologics for chronic rhinosinusitis. Cochrane Database Syst Rev. 2021 Mar 12;3(3):CD013513. doi: 10.1002/14651858.CD013513.pub3.
Results Reference
derived
Links:
URL
https://www.orchidstuffynosestudy.com/
Description
Orchid Study Website
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Efficacy and Safety Study of Benralizumab in Patient With Eosinophilic Chronic Rhinosinusitis With Nasal Polyps (ORCHID)
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