search
Back to results

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
AstraZeneca
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  1. Female or male patients aged 18 to 75 years inclusive
  2. Stable Intranasal corticosteroids (INCS) use for at least 4 weeks prior to enrolment and throughout screening
  3. History of treatment with systemic corticosteroids (SCS) or prior surgery for CRSwNP
  4. Bilateral sinonasal polyposis with a nasal polyp score (NPS) of 5 at enrolment and randomization (unilateral score of at least 2 for each nostril)
  5. Ongoing symptoms for at least 12 weeks prior to enrolment
  6. Patient-reported moderate to severe nasal blockage score (NBS) ≥2 at enrolment
  7. Bi-weekly mean NBS ≥ 1.5 at randomization
  8. SNOT-22 total score ≥ 20 at enrolment and randomization
  9. Documented physician-diagnosed asthma
  10. Blood eosinophil count of >2% or ≥150/μL at enrolment

Exclusion criteria:

  1. Any nasal and/or sinus surgery within 3 months prior to enrolment
  2. 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;
  3. Clinically important comorbidities that may put the patient at risk, or may confound interpretation of clinical efficacy and/or safety results
  4. Receipt of SCS for within 4 weeks prior to screening, or a scheduled SCS treatment during the study period.
  5. Receipt of any marketed or investigational biologic product within 6 months of enrolment
  6. Currently pregnant or breastfeeding

Sites / Locations

  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site

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

First Posted
October 23, 2019
Last Updated
August 31, 2023
Sponsor
AstraZeneca
search

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
Facility Information:
Facility Name
Research Site
City
Huntington Beach
State/Province
California
ZIP/Postal Code
92647
Country
United States
Facility Name
Research Site
City
Grand Junction
State/Province
Colorado
ZIP/Postal Code
81501
Country
United States
Facility Name
Research Site
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32605
Country
United States
Facility Name
Research Site
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40220
Country
United States
Facility Name
Research Site
City
White Marsh
State/Province
Maryland
ZIP/Postal Code
21162
Country
United States
Facility Name
Research Site
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Facility Name
Research Site
City
White Plains
State/Province
New York
ZIP/Postal Code
10605
Country
United States
Facility Name
Research Site
City
Tulsa
State/Province
Oklahoma
ZIP/Postal Code
74136
Country
United States
Facility Name
Research Site
City
Bethlehem
State/Province
Pennsylvania
ZIP/Postal Code
18017
Country
United States
Facility Name
Research Site
City
Fort Worth
State/Province
Texas
ZIP/Postal Code
76109
Country
United States
Facility Name
Research Site
City
McKinney
State/Province
Texas
ZIP/Postal Code
75070
Country
United States
Facility Name
Research Site
City
Saint George
State/Province
Utah
ZIP/Postal Code
84790
Country
United States
Facility Name
Research Site
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23235
Country
United States
Facility Name
Research Site
City
Bellingham
State/Province
Washington
ZIP/Postal Code
98225
Country
United States
Facility Name
Research Site
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53228
Country
United States
Facility Name
Research Site
City
Buenos Aires
ZIP/Postal Code
C1121 ABE
Country
Argentina
Facility Name
Research Site
City
Buenos Aires
ZIP/Postal Code
C1414AIF
Country
Argentina
Facility Name
Research Site
City
Ciudad de Buenos Aire
ZIP/Postal Code
C1425BEN
Country
Argentina
Facility Name
Research Site
City
San Fernando
ZIP/Postal Code
B1646EBJ
Country
Argentina
Facility Name
Research Site
City
Herston
ZIP/Postal Code
4029
Country
Australia
Facility Name
Research Site
City
Melbourne
ZIP/Postal Code
3004
Country
Australia
Facility Name
Research Site
City
Spearwood
ZIP/Postal Code
6163
Country
Australia
Facility Name
Research Site
City
Bruxelles
ZIP/Postal Code
1200
Country
Belgium
Facility Name
Research Site
City
Gent
ZIP/Postal Code
9000
Country
Belgium
Facility Name
Research Site
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Facility Name
Research Site
City
Plovdiv
ZIP/Postal Code
4001
Country
Bulgaria
Facility Name
Research Site
City
Sofia
ZIP/Postal Code
1303
Country
Bulgaria
Facility Name
Research Site
City
Sofia
ZIP/Postal Code
1606
Country
Bulgaria
Facility Name
Research Site
City
Quillota
ZIP/Postal Code
2260000
Country
Chile
Facility Name
Research Site
City
Santiago
ZIP/Postal Code
7500588
Country
Chile
Facility Name
Research Site
City
Santiago
ZIP/Postal Code
8150000
Country
Chile
Facility Name
Research Site
City
Talca
ZIP/Postal Code
3465584
Country
Chile
Facility Name
Research Site
City
Beijing
ZIP/Postal Code
100044
Country
China
Facility Name
Research Site
City
Beijing
ZIP/Postal Code
100191
Country
China
Facility Name
Research Site
City
Beijing
ZIP/Postal Code
100730
Country
China
Facility Name
Research Site
City
Changchun
ZIP/Postal Code
130061
Country
China
Facility Name
Research Site
City
Changsha
ZIP/Postal Code
410008
Country
China
Facility Name
Research Site
City
Changsha
ZIP/Postal Code
410013
Country
China
Facility Name
Research Site
City
Changsha
Country
China
Facility Name
Research Site
City
Chengdu
ZIP/Postal Code
610041
Country
China
Facility Name
Research Site
City
Chengdu
ZIP/Postal Code
610072
Country
China
Facility Name
Research Site
City
Chongqing
ZIP/Postal Code
400042
Country
China
Facility Name
Research Site
City
Foshan
ZIP/Postal Code
528000
Country
China
Facility Name
Research Site
City
Guangzhou
ZIP/Postal Code
510000
Country
China
Facility Name
Research Site
City
Guangzhou
ZIP/Postal Code
510180
Country
China
Facility Name
Research Site
City
Hangzhou
ZIP/Postal Code
310003
Country
China
Facility Name
Research Site
City
Jinan
ZIP/Postal Code
250014
Country
China
Facility Name
Research Site
City
Nanchang
ZIP/Postal Code
330006
Country
China
Facility Name
Research Site
City
Nanjing
ZIP/Postal Code
210029
Country
China
Facility Name
Research Site
City
Nanning
ZIP/Postal Code
530021
Country
China
Facility Name
Research Site
City
Qingdao
ZIP/Postal Code
266071
Country
China
Facility Name
Research Site
City
Shanghai
ZIP/Postal Code
200065
Country
China
Facility Name
Research Site
City
Shanghai
ZIP/Postal Code
200092
Country
China
Facility Name
Research Site
City
Tianjin
ZIP/Postal Code
300052
Country
China
Facility Name
Research Site
City
Urumqi
ZIP/Postal Code
830054
Country
China
Facility Name
Research Site
City
Wuhan
ZIP/Postal Code
430022
Country
China
Facility Name
Research Site
City
Xi'an
ZIP/Postal Code
710004
Country
China
Facility Name
Research Site
City
Xian
ZIP/Postal Code
710061
Country
China
Facility Name
Research Site
City
Yantai
ZIP/Postal Code
264000
Country
China
Facility Name
Research Site
City
Marseille
ZIP/Postal Code
13005
Country
France
Facility Name
Research Site
City
Toulouse CEDEX 09
ZIP/Postal Code
31059
Country
France
Facility Name
Research Site
City
Budapest
ZIP/Postal Code
1033
Country
Hungary
Facility Name
Research Site
City
Budapest
ZIP/Postal Code
1046
Country
Hungary
Facility Name
Research Site
City
Győr
ZIP/Postal Code
9024
Country
Hungary
Facility Name
Research Site
City
Kaposvár
ZIP/Postal Code
7400
Country
Hungary
Facility Name
Research Site
City
Siófok
ZIP/Postal Code
8600
Country
Hungary
Facility Name
Research Site
City
Székesfehérvár
ZIP/Postal Code
8000
Country
Hungary
Facility Name
Research Site
City
Tatabánya
ZIP/Postal Code
2800
Country
Hungary
Facility Name
Research Site
City
Catanzaro
ZIP/Postal Code
88100
Country
Italy
Facility Name
Research Site
City
Pisa
ZIP/Postal Code
56124
Country
Italy
Facility Name
Research Site
City
Roma
ZIP/Postal Code
00161
Country
Italy
Facility Name
Research Site
City
Roma
ZIP/Postal Code
00168
Country
Italy
Facility Name
Research Site
City
Chiba-shi
ZIP/Postal Code
262-0015
Country
Japan
Facility Name
Research Site
City
Fujisawa-shi
ZIP/Postal Code
251-0052
Country
Japan
Facility Name
Research Site
City
Hiroshima-shi
ZIP/Postal Code
734-8551
Country
Japan
Facility Name
Research Site
City
Ichikawa-shi
ZIP/Postal Code
272-0143
Country
Japan
Facility Name
Research Site
City
Iida-shi
ZIP/Postal Code
395-8505
Country
Japan
Facility Name
Research Site
City
Kawasaki-shi
ZIP/Postal Code
211-0063
Country
Japan
Facility Name
Research Site
City
Kumamoto-shi
ZIP/Postal Code
860-0814
Country
Japan
Facility Name
Research Site
City
Meguro-ku
ZIP/Postal Code
153-0061
Country
Japan
Facility Name
Research Site
City
Meguro-ku
ZIP/Postal Code
153-8515
Country
Japan
Facility Name
Research Site
City
Minato-ku
ZIP/Postal Code
105-8471
Country
Japan
Facility Name
Research Site
City
Moriguchi-shi
ZIP/Postal Code
570-0074
Country
Japan
Facility Name
Research Site
City
Nagaoka-shi
ZIP/Postal Code
940-2085
Country
Japan
Facility Name
Research Site
City
Osaka-shi
ZIP/Postal Code
540-0008
Country
Japan
Facility Name
Research Site
City
Shinjuku-ku
ZIP/Postal Code
160-0017
Country
Japan
Facility Name
Research Site
City
Yoshida-gun
ZIP/Postal Code
910-1193
Country
Japan
Facility Name
Research Site
City
Bydgoszcz
ZIP/Postal Code
85-231
Country
Poland
Facility Name
Research Site
City
Elbląg
ZIP/Postal Code
82-300
Country
Poland
Facility Name
Research Site
City
Kraków
ZIP/Postal Code
31-513
Country
Poland
Facility Name
Research Site
City
Lublin
ZIP/Postal Code
20-552
Country
Poland
Facility Name
Research Site
City
Nadarzyn
ZIP/Postal Code
05-830
Country
Poland
Facility Name
Research Site
City
Poznań
ZIP/Postal Code
60-805
Country
Poland
Facility Name
Research Site
City
Wrocław
ZIP/Postal Code
53-301
Country
Poland
Facility Name
Research Site
City
Łodź
ZIP/Postal Code
90-153
Country
Poland
Facility Name
Research Site
City
Izhevsk
ZIP/Postal Code
426061
Country
Russian Federation
Facility Name
Research Site
City
Penza
ZIP/Postal Code
440067
Country
Russian Federation
Facility Name
Research Site
City
Saint-Petersburg
ZIP/Postal Code
196158
Country
Russian Federation
Facility Name
Research Site
City
Taipei City
ZIP/Postal Code
110
Country
Taiwan
Facility Name
Research Site
City
Taipei City
ZIP/Postal Code
11217
Country
Taiwan
Facility Name
Research Site
City
Taipei City
ZIP/Postal Code
114
Country
Taiwan
Facility Name
Research Site
City
Taipei
ZIP/Postal Code
10002
Country
Taiwan
Facility Name
Research Site
City
Taipei
ZIP/Postal Code
235
Country
Taiwan
Facility Name
Research Site
City
Taoyuan
ZIP/Postal Code
333
Country
Taiwan
Facility Name
Research Site
City
Bangkok
ZIP/Postal Code
10330
Country
Thailand
Facility Name
Research Site
City
Bangkok
ZIP/Postal Code
10400
Country
Thailand
Facility Name
Research Site
City
Bangkok
ZIP/Postal Code
10700
Country
Thailand
Facility Name
Research Site
City
Chiang Mai
ZIP/Postal Code
50200
Country
Thailand
Facility Name
Research Site
City
Khon Kaen
ZIP/Postal Code
40002
Country
Thailand
Facility Name
Research Site
City
Phitsanulok
ZIP/Postal Code
65000
Country
Thailand
Facility Name
Research Site
City
Aydin
ZIP/Postal Code
09100
Country
Turkey
Facility Name
Research Site
City
Bakirkoy
ZIP/Postal Code
34147
Country
Turkey
Facility Name
Research Site
City
Izmir
ZIP/Postal Code
35340
Country
Turkey
Facility Name
Research Site
City
Malatya
ZIP/Postal Code
44280
Country
Turkey
Facility Name
Research Site
City
Hanoi
ZIP/Postal Code
100000
Country
Vietnam
Facility Name
Research Site
City
Ho Chi Minh
ZIP/Postal Code
700000
Country
Vietnam

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

Learn more about this trial

Efficacy and Safety Study of Benralizumab in Patient With Eosinophilic Chronic Rhinosinusitis With Nasal Polyps (ORCHID)

We'll reach out to this number within 24 hrs