Study of CM310 in Patients With Uncontrolled Seasonal Allergic Rhinitis
Condition(s) studied
Investigational drug(s) / intervention(s)
Interleukin-4 receptor responders: Interleukin-4 receptor was injected subcutaneously.
Placebo: Placebo was injected subcutaneously.
Study 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
Primary outcome measure(s)
- Average change from baseline in daily retrospective total nasal symptom score (rTNSS) at week 2. — up to Week 2
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.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beijing Tongren Hospital, Capital Medical University | Beijing | Beijing Municipality | Recruiting |
More Beijing Tongren Hospital trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06300203 on ClinicalTrials.gov ↗ ← All trials in China