Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06741800

Microbial Study of Sublingual Immunotherapy Tablets in Patients With Allergic Rhinitis

Microbial Characterization in Patients With Allergic Rhinitis Before and After Sublingual Immunotherapy Tablets

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
The First Affiliated Hospital with Nanjing Medical University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The incidence of allergic rhinitis (AR) in Chinese adults was reported to be as high as 24.1% and 16.8% in children. The current symptomatic treatment has the disadvantage of poor efficacy and cannot change the natural course of the disease. Allergen immunotherapy (AIT) is the only causative treatment approved by the WHO, bringing a new option to patients with allergic diseases. The quality of allergen preparations is critical to the diagnosis and treatment of the disease, emphasizing the need for standardized preparations, and AIT treatment in the early stages of the disease may change the long-term progression of the disease. Recent studies have reported that the microbiome of patients with different efficacy of desensitization therapy is different and may be correlated with the clinical symptoms of patients, but no prospective studies have been reported.

Conditions

Interventions

TypeNameDescription
DRUGACARIZAX®️ACARIZAX®️:The recommended dose for adults (18-65 years) is one freeze-dried tablet (12 SQ-HDM) daily, placed under the tongue.

Timeline

Start date
2024-12-20
Primary completion
2028-07-01
Completion
2032-07-01
First posted
2024-12-19
Last updated
2024-12-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06741800. Inclusion in this directory is not an endorsement.