NCT Number: NCT00092144
Study of an Approved Drug in Patients With Asthma (0476-289)(COMPLETED)
The purpose of this study is to assess the efficacy and safety of an approved drug on asthma symptoms in patients with chronic asthma which is also active during the allergy season.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Asthma symptoms brought on by allergies
Exclusion criteria
- Patient has any lung disease
- Currently have a sinus infection or cold symptoms
Treatment and study plan
Comparator: placebo / Duration of Treatment: 4 weeks
DrugPrimary outcomes
-
To assess daytime asthma symptoms as measured by daily diaries over a 3-week treatment period
Secondary outcomes
-
To assess the following over a 3-week treatment period:
-
nighttime symptoms
-
AM PEFR
-
PM PEFR
-
B-agonist use
-
asthma attacks
-
discontinuations due to asthma
Sponsors and collaborators
Lead sponsor
Organon and Co
Industry
Registry information
Official study title
A Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel-Group Study to Evaluate the Clinical Effect of Oral MK0476 Vs Placebo During the Allergy Season in Patients With Seasonal Aeroallergen Sensitivity and Chronic Asthma Which is Also Active During Allergy Season
Important dates
- Study start
- 2004
- Primary completion
- 2004
- Study completion
- 2004
- First posted
- Sep 24, 2004
- Registry last updated
- Aug 15, 2024
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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