drugset / Trial / NCT05525650

Comparative Evaluation of Safety and Immune Activity of New Immunotherapeutic Agents for HDM Allergic Rhinitis Patients

NCT05525650 ↗

Phase 1 Unknown 54 enrolled RAPHAS
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

EvaluationDrugModalityDoseRoute
Subject Dermatophagoides farinae Unknown 200 unknown —
Subject Dermatophagoides farinae Unknown 400 unknown —
Subject Dermatophagoides farinae Unknown 800 unknown —

Indications