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Phase III Clinical Trial, long term treatment with TO-204 - Subcutaneous immunotherapy in patients with HDM-sensitized allergic rhinitis and asthma

Phase 3
Conditions
Allergic rhinitis or asthma sensitized to house dust mite
Registration Number
JPRN-jRCT2080221855
Lead Sponsor
TORII PHARMACEUTICAL CO., LTD.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
30
Inclusion Criteria

1) Positive test in RAST(specific anti-HDM IgE >= Class 2)
2) Positive skin prick/scratch test against HDM allergen

Exclusion Criteria

1) Patients with clinical symptoms of perennial rhinitis or asthma caused by allergen other than HDM
2) Patients with severe asthma
3) Patients with severe systemic diseases (i.e., auto-immune disease, immunocomplex disease, immunodeficient disease)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Safety
Secondary Outcome Measures
NameTimeMethod
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