Efficacy and Safety of Mepolizumab in Adults With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)/ Eosinophilic Chronic Rhinosinusitis (ECRS) (MERIT)

A Randomised, Double-blind, Placebo Controlled, Parallel Group Phase III Study to Assess the Clinical Efficacy and Safety of 100 mg SC Mepolizumab in Adults With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP) / Eosinophilic Chronic Rhinosinusitis (ECRS) MERIT: Mepolizumab in Eosinophilic Chronic RhinosinusITis Study

This is a randomized, double blind, placebo controlled, parallel group phase III study designed to assess the clinical efficacy and safety of 100 milligrams (mg) subcutaneous (SC) mepolizumab treatment in adults with CRSwNP/ECRS for the purpose of registration in Japan and China. Approximately 160 participants will be randomized in a 1:1 ratio to receive either 100 mg SC mepolizumab or placebo SC. The study will include a 4-week run-in period followed by randomization to a 52-week treatment period, where participants will be administered 4-weekly doses of mepolizumab or placebo via a pre-filled safety syringe device (SSD) injection.

Study Overview

• Status: Completed
• Conditions: Nasal Polyps
• Intervention / Treatment: Drug: Mepolizumab; Drug: Standard of care; Drug: Placebo

• Study Type: Interventional
• Enrollment (Actual): 169
• Phase: Phase 3

Contacts and Locations

Study Locations

• China
  • Beijing, China, 100191
    • GSK Investigational Site
  • Beijing, China, 100730
    • GSK Investigational Site
  • Chengdu, China, 610041
    • GSK Investigational Site
  • Shanghai, China, 200030
    • GSK Investigational Site
  • Shanghai, China, 200003
    • GSK Investigational Site
  • Wuhan, China, 430022
    • GSK Investigational Site
  • Xiamen, China, 361004
    • GSK Investigational Site
  • Yantai, China, 264000
    • GSK Investigational Site
  • Guangdong
    • Dongguan, Guangdong, China, 523326
      • GSK Investigational Site
    • Guangzhou, Guangdong, China, 510000
      • GSK Investigational Site
    • Zhongshan, Guangdong, China, 528400
      • GSK Investigational Site
  • Hainan
    • Haikou, Hainan, China, 570311
      • GSK Investigational Site
  • Hubei
    • Wuhan, Hubei, China, 430060
      • GSK Investigational Site
  • Jiangsu
    • Nanjing, Jiangsu, China, 210029
      • GSK Investigational Site
  • Shandong
    • Qingdao, Shandong, China, 266061
      • GSK Investigational Site
    • Zibo, Shandong, China, 255036
      • GSK Investigational Site
  • Shanxi
    • Taiyuan, Shanxi, China, 300201
      • GSK Investigational Site
• Japan
  • Aichi, Japan, 457-8511
    • GSK Investigational Site
  • Aichi, Japan, 464-8547
    • GSK Investigational Site
  • Aichi, Japan, 471-8513
    • GSK Investigational Site
  • Chiba, Japan, 262-0015
    • GSK Investigational Site
  • Chiba, Japan, 272-0143
    • GSK Investigational Site
  • Fukui, Japan, 910-1193
    • GSK Investigational Site
  • Fukuoka, Japan, 810-0001
    • GSK Investigational Site
  • Fukuoka, Japan, 806-8501
    • GSK Investigational Site
  • Hiroshima, Japan, 734-8551
    • GSK Investigational Site
  • Hyogo, Japan, 663-8501
    • GSK Investigational Site
  • Hyogo, Japan, 665-0827
    • GSK Investigational Site
  • Ibaraki, Japan, 309-1793
    • GSK Investigational Site
  • Ishikawa, Japan, 920-0293
    • GSK Investigational Site
  • Kagawa, Japan, 763-8502
    • GSK Investigational Site
  • Kagoshima, Japan, 890-0062
    • GSK Investigational Site
  • Kanagawa, Japan, 232-0024
    • GSK Investigational Site
  • Kanagawa, Japan, 211-8533
    • GSK Investigational Site
  • Kanagawa, Japan, 250-8558
    • GSK Investigational Site
  • Kumamoto, Japan, 860-0814
    • GSK Investigational Site
  • Kyoto, Japan, 602-8026
    • GSK Investigational Site
  • Kyoto, Japan, 600-8216
    • GSK Investigational Site
  • Mie, Japan, 514-8507
    • GSK Investigational Site
  • Miyagi, Japan, 983-8512
    • GSK Investigational Site
  • Nagano, Japan, 395-8505
    • GSK Investigational Site
  • Niigata, Japan, 940-2085
    • GSK Investigational Site
  • Okayama, Japan, 701-0192
    • GSK Investigational Site
  • Osaka, Japan, 570-8507
    • GSK Investigational Site
  • Osaka, Japan, 565-0871
    • GSK Investigational Site
  • Osaka, Japan, 569-8686
    • GSK Investigational Site
  • Osaka, Japan, 583-8588
    • GSK Investigational Site
  • Tokyo, Japan, 142-8666
    • GSK Investigational Site
  • Tokyo, Japan, 113-8655
    • GSK Investigational Site
  • Tokyo, Japan, 141-0001
    • GSK Investigational Site
  • Tokyo, Japan, 153-8515
    • GSK Investigational Site
  • Tokyo, Japan, 160-0023
    • GSK Investigational Site
  • Tokyo, Japan, 143-8541
    • GSK Investigational Site
  • Tokyo, Japan, 162-8543
    • GSK Investigational Site
• Russian Federation
  • Moscow, Russian Federation, 119991
    • GSK Investigational Site
  • Moscow, Russian Federation, 108840
    • GSK Investigational Site
  • Saint Petersburg, Russian Federation, 197022
    • GSK Investigational Site
  • Saint-Petersburg, Russian Federation, 190013
    • GSK Investigational Site
  • Saint-Petersburg, Russian Federation, 196158
    • GSK Investigational Site
  • St. Petersburg, Russian Federation, 194356
    • GSK Investigational Site
  • Yaroslavl, Russian Federation, 150003
    • GSK Investigational Site

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Participants of 18 years of age and older inclusive, at the time of signing the informed consent.
• Body weight greater than or equal to 40 kilograms (kg).
• Male or female participants (with appropriate contraceptive methods) to be eligible for entry into the study.
• Female participant is eligible to participate if she is not pregnant or breastfeeding, one of the following conditions applies:
• Is a woman of non- childbearing potential (WONCBP) : or
• Is a woman of child bearing potential (WOCBP) and using a contraceptive method that is highly effective [with a failure rate of less than (<)1percent (%) per year], preferably with low user dependency, during the study intervention period and for at least 105 days after the last dose of study intervention. The investigator should evaluate the potential for contraceptive method failure (for example [e.g.] noncompliance, recently initiated) in relationship to the first dose of study intervention.
• A WOCBP must have a negative highly sensitive urine pregnancy test within 24 hours before the first dose of study intervention.
• If a urine test cannot be confirmed as negative (e.g., an ambiguous result), a serum pregnancy test is required. In such cases, the participant must be excluded from participation if the serum pregnancy result is positive.
• The investigator is responsible for review of medical history, menstrual history, and recent sexual activity to decrease the risk for inclusion of a woman with an early undetected pregnancy.
• A documented blood eosinophil count of over 2% in the 12 months prior to Visit 0 or through a blood sample taken between Visit 0 and Visit 1. All participants must meet blood eosinophil count of over 2% by Visit 1. Participants with peripheral blood eosinophil count over 2% to 5% must also have comorbid bronchial asthma, aspirin intolerance, or nonsteroidal anti-inflammatory drug intolerance at Visit 1 assessment in order to return for Visit 2.
• Endoscopic bilateral NP score of at least 5 out of a maximum score of 8 (with a minimum score of 2 in each nasal cavity) assessed by the investigator.
• Participants who have had at least one of the following at Visit 1: previous nasal surgery for the removal of NP; have used at least three consecutive days of systemic corticosteroids in the previous 2 years for the treatment of NP: medically unsuitable or intolerant to systemic corticosteroid.
• Participants with severe NP symptoms defined as a nasal obstruction VAS symptom score of greater than (>)5.
• Presence of symptoms of CRS as described by at least two different symptoms for at least 12 weeks prior to Visit 1, one of which should be either nasal blockage/obstruction/congestion or nasal discharge (anterior/posterior nasal drip), plus facial pain/pressure, and/or reduction or loss of smell
• Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and study protocol.

Exclusion Criteria:

• As a result of medical interview, physical examination, or screening investigation the physician responsible considers the participant unfit for the study. (e.g. symptomatic herpes zoster within 3 months prior to screening, evidence of tuberculosis [TB] active or latent).
• Cystic fibrosis
• Eosinophilic granulomatosis with polyangiitis (also known as Churg Strauss syndrome), Young's, Kartagener's or dyskinetic ciliary syndromes.
• Antrochoanal polyps.
• Severe nasal septal deviation preventing full assesment of nasal polyps in both nostrils.
• Acute sinusitis or upper respiratory tract infection (URTI) at screening or in 2 weeks prior to screening.
• Ongoing rhinitis medicamentosa (rebound or chemical induced rhinitis).
• Participants who have had an asthma exacerbation requiring admission to hospital within 4 weeks of screening.
• Participants who have undergone any intranasal and/or sinus surgery (for example polypectomy, balloon dilatation or nasal stent insertion) within 6 months prior to Visit 1.
• Participants where NP surgery is contraindicated in the opinion of the Investigator.
• Participants with a known medical history of Human Immunodeficiency Virus (HIV) infection.
• Participants with a known, pre-existing parasitic infestation within 6 months prior to Visit 1.
• Participants who are currently receiving or have received within 3 months (or 5 half-lives - whatever is the longest) prior to first mepolizumab dose, chemotherapy, radiotherapy or investigational medications/therapies.
• Participants with a history of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GlaxoSmithKline (GSK) Medical Monitor, contraindicates their participation. Aspirin sensitive participants are acceptable.
• Participants with a history of allergic reaction to anti-IL-5 or other monoclonal antibody therapy.
• Participants that have taken part in previous mepolizumab clinical studies.
• Participants currently using intranasal corticosteroids (INCS) and inhaled corticosteroids exhalation through nose (ICS/ETN) for the management of their ECRS who are not willing to maintain using this method of administration throughout the study.
• Use of systemic corticosteroids (including oral corticosteroids) or corticosteroid nasal solution (intranasal corticosteroid is excepted) within 4 weeks prior to screening or planned use of such medications during the double-blind period.
• INCS and/or inhaled corticosteroids exhalation through nose (ICS/ETN) dose changes within 1 month prior to Visit 1 (if applicable).
• Treatments with biological or immunosuppressive treatment (other than Xolair) treatment within 5 terminal phase half-lives of Visit 1.
• Omalizumab (Xolair) treatment in the 130 days prior to Visit 1.
• Commencement or change of dose of leukotriene antagonist treatment less than 30 days prior to Visit 1.
• Commencement or change of dose of allergen immunotherapy within the previous 3 months.
• Women who are pregnant or lactating or are planning on becoming pregnant during the study.
• Any participant who is considered unlikely to survive the duration of the study period or has any rapidly progressing disease or immediate life-threatening illness (e.g. cancer). In addition, any participant who has any other condition (e.g. neurological condition) that is likely to affect respiratory function should not be included in the study.
• Participants who have known, pre-existing, clinically significant endocrine, autoimmune, cardiovascular, metabolic, neurological, renal, gastrointestinal, hepatic, hematological or any other system abnormalities that are uncontrolled with standard treatment.
• Participants with symptoms suggestive of active Coronavirus Disease-2019 (COVID-19) infection (that is fever, cough etc) are excluded.
• Participants with known COVID-19 positive contacts within the past 14 days should be excluded for at least 14 days since the exposure and the participant remains symptom free.
• A known immunodeficiency (e.g. HIV), other than that explained by the use of corticosteroids taken as therapy.
• A current malignancy or previous history of cancer in remission for less than 12 months prior to screening.
• Current active liver or biliary disease (with the exception of Gilbert's syndrome or asymptomatic gallstones or otherwise stable chronic liver disease per investigator assessment).
• Alanine aminotransferase (ALT) >2 times Upper limit of normal (ULN).
• Bilirubin >1.5 times ULN (isolated bilirubin >1.5 times ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).
• Current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminemia, esophageal or gastric varices, persistent jaundice, or cirrhosis.
• Participants with a QT interval, from the electrocardiogram (ECG) conducted at Screening Visit 1, corrected with Fridericia's formula (QTcF) >450 milliseconds (msec) (or QTcF >480msec in participants with bundle branch block).
• Known or suspected history of alcohol or drug abuse within 2 years prior to Screening (Visit 1) that in the opinion of the investigator would prevent the participant from completing the study procedures.
• Is an investigator, sub-investigator, and study coordinator, employee of a participating investigator or study site, or immediate family member of the aforementioned that is involved in this study.
• In the opinion of the investigator, any participant who is unable to read and/or would not be able to complete a questionnaire.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Participants receiving mepolizumab + Standard of care (SoC); Participants will receive one dose of 100 mg mepolizumab SC on top of SoC every 4 weeks during the 52-week treatment period.	Drug: Mepolizumab; Mepolizumab will be available as a clear to opalescent, colorless solution for SC injection in a single-use, safety syringe at a unit dose strength of 100 mg/milliliters (mL).; Drug: Standard of care; Participants will continue to receive Standard of care as they are used to before entry in the study.
Placebo Comparator: Participants receiving placebo + SoC; Participants will receive one dose of placebo via SC route on top of SoC, every 4 weeks during the 52-week treatment period.	Drug: Standard of care; Participants will continue to receive Standard of care as they are used to before entry in the study.; Drug: Placebo; Placebo will be available as a clear to opalescent, colorless sterile solution for SC injection in a single-use, safety syringe

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change from Baseline in total endoscopic NP score at Week 52 (scores on a scale)	NP score is graded and based on NP size recorded as the sum of the right and left nostril scores with a range of 0-8; higher scores indicate worse status. Individual score ranges from 0 (no polyps) to 4 (large polyps causing almost complete congestion/ obstruction of the inferior meatus) within each nostril.	Baseline (Day 0) and at Week 52
Change from Baseline in mean nasal obstruction visual analogue scale (VAS) score (scores on a scale)	Participant will be asked to indicate on a VAS the severity of 5 nasal polyposis symptoms (one VAS for each symptom) and symptoms overall: 1. nasal obstruction; 2. nasal discharge; 3. mucus in the throat; 4. loss of smell; 5. Facial pain; 6. overall VAS symptoms score. The left-hand side of the scale (0) represents "None" and the right-hand side of the scale (100) represents "As bad as you can imagine". The participant selects a point on the line that represents their current state on the continuum. VAS will be collected using an electronic Diary, suitably pixilated to allow the selection of all integers from 0 to 100.	Baseline (Day 0) and up to 52 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change from Baseline in sino-nasal outcome test (SNOT)-22 total score at Week 52 (scores on a scale)	SNOT-22 is a 22-item measure of disease specific health related quality of life (HRQoL). Participants will be asked to rate the severity of their condition on each of the 22 items over the previous 2 weeks using a 6-point rating scale of 0-5 including: 0 =Not present/no problem; 1 =Very mild problem; 2 = Mild or slight problem; 3 = Moderate problem; 4 = Severe problem; 5=Problem as "bad as it can be". The total score range for the SNOT-22 is 0-110, where higher scores indicate greater disease impact.	Baseline (Day 0) and at Week 52
Change from Baseline in mean overall VAS symptom score (scores on a scale)	Participant will be asked to indicate on a VAS the severity of 5 nasal polyposis symptoms (one VAS for each symptom) and symptoms overall: 1. nasal obstruction; 2. nasal discharge; 3. mucus in the throat; 4. loss of smell; 5. Facial pain; 6. overall VAS symptoms score. The left-hand side of the scale (0) represents "None" and the right-hand side of the scale (100) represents "As bad as you can imagine". The participant selects a point on the line that represents their current state on the continuum. VAS will be collected using an electronic Diary, suitably pixilated to allow the selection of all integers from 0 to 100.	Baseline (Day 0) and up to 52 weeks
Change from Baseline in the mean composite VAS score [combining VAS scores for nasal obstruction, nasal discharge, mucus in the throat and loss of smell] (scores on a scale)	Participant will be asked to indicate on a VAS the severity of 5 nasal polyposis symptoms (one VAS for each symptom) and symptoms overall: 1. nasal obstruction; 2. nasal discharge; 3. mucus in the throat; 4. loss of smell; 5. Facial pain; 6. overall VAS symptoms score. The left-hand side of the scale (0) represents "None" and the right-hand side of the scale (100) represents "As bad as you can imagine". The participant selects a point on the line that represents their current state on the continuum. VAS will be collected using an electronic Diary, suitably pixilated to allow the selection of all integers from 0 to 100.	Baseline (Day 0) and up to 52 weeks
Change from Baseline in Lund Mackay (LMK) computed tomography (CT) score at Week 52 (scores on a scale)	The LMK CT scoring system is based on localization with points given for degree of opacification: 0 =normal, 1 = partial opacification, 2 = total opacification. These points are then applied to the maxillary, anterior ethmoid, posterior ethmoid, sphenoid, frontal sinus on each side. The osteomeatal complex (OC) is graded as 0 = not occluded, or 2 = occluded deriving a maximum score of 12 per side. The range for the LMK CT score is therefore 0-24 when summed across both sides.	Baseline (Day 0) and at Week 52
Change from Baseline in mean individual VAS symptom score for loss of smell (scores on a scale)	Participant will be asked to indicate on a VAS the severity of 5 nasal polyposis symptoms (one VAS for each symptom) and symptoms overall: 1. nasal obstruction; 2. nasal discharge; 3. mucus in the throat; 4. loss of smell; 5. Facial pain; 6. overall VAS symptoms score. The left-hand side of the scale (0) represents "None" and the right-hand side of the scale (100) represents "As bad as you can imagine". The participant selects a point on the line that represents their current state on the continuum. VAS will be collected using an electronic Diary, suitably pixilated to allow the selection of all integers from 0 to 100.	Baseline (Day 0) and up to 52 weeks
Time to first nasal surgery or course of systemic corticosteroids (CS) for CRSwNP/ECRS up to Week 52	NP surgery is defined as any procedure involving instruments resulting in incision and removal of tissue from the nasal cavity (for example polypectomy). Additionally, the number of courses of systemic steroids and reason for treatment will be recorded throughout the study.	Up to 52 weeks

Collaborators and Investigators

• Sponsor: GlaxoSmithKline
• Collaborators: BioClinica, Inc.; Signant Health
• Investigators: Study Director: GSK Clinical Trials, GlaxoSmithKline

Study record dates

Study Major Dates

• Study Start (Actual): February 8, 2021
• Primary Completion (Actual): April 12, 2023
• Study Completion (Actual): April 12, 2023

Study Registration Dates

• First Submitted: October 23, 2020
• First Submitted That Met QC Criteria: October 23, 2020
• First Posted (Actual): October 28, 2020

Study Record Updates

• Last Update Posted (Actual): February 14, 2024
• Last Update Submitted That Met QC Criteria: February 13, 2024
• Last Verified: February 1, 2024

More Information

Terms related to this study

• Keywords: Mepolizumab; Chronic rhinosinusitis; Eosinophilic chronic rhinosinusitis
• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Pathological Conditions, Anatomical; Nose Diseases; Nasal Polyps; Polyps
• Other Study ID Numbers: 209692

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: IPD for this study will be made available via the Clinical Study Data Request site.
• IPD Sharing Time Frame: IPD will be made available within 6 months of publishing the results of the primary endpoints, key secondary endpoints and safety data of the study.
• IPD Sharing Access Criteria: Access is provided after a research proposal is submitted and has received approval from the Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months but an extension can be granted, when justified, for up to another 12 months.
• IPD Sharing Supporting Information Type: STUDY_PROTOCOL; SAP; ICF; CSR

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No