A Study of CM310 in Patients With Uncontrolled Seasonal Allergic Rhinitis (MERAK)
Primary Purpose
Allergic Rhinitis
Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Interleukin-4 receptor responders 1
Interleukin-4 receptor responders 2
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Allergic Rhinitis
Eligibility Criteria
Inclusion Criteria:
- Voluntarily sign the informed consent form.
Exclusion Criteria:
- Have any condition that are not suitable for participating in this study.
Sites / Locations
- Beijing Tongren Hospital, Capital Medical University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Interleukin-4 receptor responders 1
Interleukin-4 receptor responders 2
Controls
Arm Description
Interleukin-4 receptor was injected subcutaneously, once every two weeks.
Interleukin-4 receptor was injected subcutaneously, once a week.
Placebo was injected subcutaneously.
Outcomes
Primary Outcome Measures
Average change from baseline in daily retrospective total nasal symptom score (rTNSS) during treatment period.
Average change from baseline in daily retrospective total nasal symptom score (rTNSS) during treatment period. The Total Nasal Symptom Score (TNSS) is the sum of the four symptom scores of runny nose, nasal congestion, nasal itching, and sneezing, with each symptom scoring from 0 to 3.
Secondary Outcome Measures
Full Information
NCT ID
NCT05470647
First Posted
July 19, 2022
Last Updated
October 17, 2023
Sponsor
Beijing Tongren Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05470647
Brief Title
A Study of CM310 in Patients With Uncontrolled Seasonal Allergic Rhinitis
Acronym
MERAK
Official Title
The Efficacy and Safety of CM310 Injection in Patients With Uncontrolled Seasonal Allergic Rhinitis Under Conventional Treatment: A Randomized, Double-Blind, Placebo-controlled Investigator Initiated Trial (IIT) Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
August 17, 2022 (Actual)
Primary Completion Date
September 24, 2022 (Actual)
Study Completion Date
December 28, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Beijing Tongren Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Allergic rhinitis (AR) is a non-infectious chronic inflammatory disease of the nasal mucosa mainly mediated by immunoglobulin E after exposure to allergens in atopic individuals. The typical symptoms of AR are paroxysmal sneezing, watery rhinorrhea, itching, and nasal congestion, which may be accompanied by ocular symptoms, including eye itching, tearing, redness, and burning sensation, which are more common in patients with hay fever allergies. Bronchial asthma is associated with bronchial asthma in 40% of patients with AR, suggesting a comorbid feature of allergic disease.
Detailed Description
AR is a common clinical chronic nasal disease, affecting 10% to 20% of the world's population, and has become a global health problem. AR not only seriously affects the quality of life of patients, resulting in patient fatigue, impaired learning, attention, and decision-making ability, but also causes a heavy social burden.
AR has a variety of classification methods. According to the type of allergen, it can be divided into seasonal (SAR, common allergens are seasonal allergens such as pollen) and perennial (PAR, common allergens are indoor allergens such as dust mites or occupational allergies), which is a classification method often used in clinical studies. According to the course of the disease, it can be divided into intermittent (symptom onset < 4 days/week, or < 4 consecutive weeks) and persistent (symptom onset ≥ 4 days/week, and ≥ 4 consecutive weeks). According to the severity of the disease, it can be divided into minor AR (mild symptoms, with no significant impact on quality of life) and moderate-severe AR (more severe or severe symptoms, with significant impact on quality of life). The results of the cooperative survey showed that persistent moderate-to-severe disease was the most common in the overall population, accounting for 52.2%, indicating that the treatment and control of AR has become an urgent problem to be solved.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Rhinitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
93 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Interleukin-4 receptor responders 1
Arm Type
Experimental
Arm Description
Interleukin-4 receptor was injected subcutaneously, once every two weeks.
Arm Title
Interleukin-4 receptor responders 2
Arm Type
Experimental
Arm Description
Interleukin-4 receptor was injected subcutaneously, once a week.
Arm Title
Controls
Arm Type
Placebo Comparator
Arm Description
Placebo was injected subcutaneously.
Intervention Type
Biological
Intervention Name(s)
Interleukin-4 receptor responders 1
Intervention Description
Interleukin-4 receptor was injected subcutaneously.
Intervention Type
Biological
Intervention Name(s)
Interleukin-4 receptor responders 2
Intervention Description
Interleukin-4 receptor was injected subcutaneously.
Intervention Type
Biological
Intervention Name(s)
Placebo
Intervention Description
Placebo was injected subcutaneously.
Primary Outcome Measure Information:
Title
Average change from baseline in daily retrospective total nasal symptom score (rTNSS) during treatment period.
Description
Average change from baseline in daily retrospective total nasal symptom score (rTNSS) during treatment period. The Total Nasal Symptom Score (TNSS) is the sum of the four symptom scores of runny nose, nasal congestion, nasal itching, and sneezing, with each symptom scoring from 0 to 3.
Time Frame
up to week 2
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Voluntarily sign the informed consent form.
Exclusion Criteria:
Have any condition that are not suitable for participating in this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luo zhang
Organizational Affiliation
Beijing Tongren Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Beijing Tongren Hospital, Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100000
Country
China
12. IPD Sharing Statement
Learn more about this trial
A Study of CM310 in Patients With Uncontrolled Seasonal Allergic Rhinitis
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