RecruitingPhase 2NCT06300203

Study of CM310 in Patients With Uncontrolled Seasonal Allergic Rhinitis

The Efficacy and Safety of Humanized Antibody Targeting the Interleukin-4 Receptor Alpha Subunit (IL-4Rα) in Patients With Uncontrolled Seasonal Allergic Rhinitis Under Standard Treatment: A Randomized, Double-Blind, Placebo-controlled IIT Study


Sponsor

Beijing Tongren Hospital

Enrollment

120 participants

Start Date

Mar 18, 2024

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a biological treatment called Interleukin-4 receptor responders and Placebo for people with seasonal allergic rhinitis. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALInterleukin-4 receptor responders

Interleukin-4 receptor was injected subcutaneously.

OTHERPlacebo

Placebo was injected subcutaneously.


Locations(1)

Beijing Tongren Hospital, Capital Medical University

Beijing, Beijing Municipality, China

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NCT06300203


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