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NCT05525650

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

ENROLLING BY INVITATION Phase 1 Last updated 10 April 2024
What this trial tests

Phase 1 trial testing House Dust Mite Extract, Dermatophagoides Farinae in Mite Allergy in 54 participants. Enrolling by invitation.

Timeline
20 January 2022
Primary endpoint
21 December 2024
15 June 2025

Quick facts

Lead sponsorRAPHAS
PhasePhase 1
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment54
Start date20 January 2022
Primary completion21 December 2024
Estimated completion15 June 2025
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

RAPHAS — full company profile →

Who can join

Adults 19 to 60, any sex, with Mite Allergy or Rhinitis, Allergic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. From mechanism to applications: Advanced microneedles for clinical medicine.
    Yang Y, Sun H, Sun X, Wang Y, et al · · 2025 · cited 9× · PMID 40463395 · DOI 10.1016/j.bioactmat.2025.04.025

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