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CompletedNCT00070707

Nasonex Compared With Placebo in Participants With Seasonal Allergic Rhinitis (SAR) and Concomitant Asthma (P03280)

Efficacy and Safety of Nasonex vs. Placebo in Subjects With SAR and Concomitant Asthma

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
188 (actual)
Sponsor
Organon and Co · Industry
Sex
All
Age
15 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study will compare mometasone nasal spray to placebo in treating the nasal and asthma symptoms experienced by participants with seasonal allergic rhinitis (SAR) and concomitant asthma.

Conditions

Interventions

TypeNameDescription
DRUGMometasoneMometasone nasal spray 200 mcg/day administered as 2 sprays (50 mcg/spray) in each nostril.
DRUGPlaceboMatching placebo nasal spray, administered QD as 2 sprays in each nostril.
DRUGAlbuterol/SalbutamolAlbuterol/salbutamol metered dose inhaler (90 mcg/puff) used as needed as asthma rescue medication.

Timeline

Start date
2003-04-03
Primary completion
2003-11-26
Completion
2003-11-26
First posted
2003-10-10
Last updated
2024-09-05
Results posted
2019-07-18

Regulatory

Source: ClinicalTrials.gov record NCT00070707. Inclusion in this directory is not an endorsement.

Nasonex Compared With Placebo in Participants With Seasonal Allergic Rhinitis (SAR) and Concomitant Asthma (P03280) (NCT00070707) · Clinical Trials Directory