Kimura'
Conditions
Interventions
a fixed schedule of eight cycles of omalizumab 300 mg, administered subcutaneously at intervals of 2 weeks
Sponsors
Tokyo Women's Medical University, Department of Otorhinolaryngolog
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. patients aged >20 years old 2. patients who are unresponsive to standard therapies 3. Levels of serum IgE >30 4. patients agreed to prior written informed consent
Exclusion criteria
Exclusion criteria: 1. patients who are hypersinsitive to omalizumab 2. pregnenat or breast feeding patients 3. patients who are considered inadequate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes of mass lesion | — |
Countries
Japan
Contacts
Public ContactEri Sakitani
Tokyo Women's Medical University Department of Otorhinolaryngology
Outcome results
None listed