drugset / Trial / NCT05525650
Comparative Evaluation of Safety and Immune Activity of New Immunotherapeutic Agents for HDM Allergic Rhinitis Patients
RandomizedParallel-groupQuadruple-blindTreatment
Summary
When administering clinical trial drugs to patients with house dust mite allergic rhinitis, safety/tolerance is comparatively evaluated as the primary outcome, and symptom improvement and immune activity of the disease are comparatively evaluated as secondary outcome.
Timeline
- Start
- 2022-01-20
- Primary completion
- 2024-12-21
- Completion
- 2025-06-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Dermatophagoides farinae | Unknown | 200 unknown | — |
| Subject | Dermatophagoides farinae | Unknown | 400 unknown | — |
| Subject | Dermatophagoides farinae | Unknown | 800 unknown | — |