Seasonal allergic rhinitis Respiratory Diseases of upper respiratory tract
Conditions
Interventions
Patients randomly assigned once-daily (QD) SCH34117 at doses of 2.5, 5, 7.5, 10, or 20 mg versus placebo for two weeks.
Sponsors
Schering-Plough Research Institute (SPRI) (USA)
Eligibility
Inclusion criteria
Inclusion criteria: Subjects 12 years or older with a two-year documented history of seasonal allergic rhinitis and otherwise in good health
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United States of America
Outcome results
None listed