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

Inclusion Criteria1

  • Voluntarily sign the informed consent form.

Exclusion Criteria1

  • Have any condition that are not suitable for participating in this study.

Interested in this trial?

Get notified about updates and connect with the research team.

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

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06300203


Related Trials