Trials / Completed
CompletedNCT00632502
Neutrophilic Asthma Study With Navarixin (MK-7123, SCH 527123) (MK-7123-017)(COMPLETED)
Safety of SCH 527123 in Subjects With Neutrophilic Asthma
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 37 (actual)
- Sponsor
- Merck Sharp & Dohme LLC · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
4-Week Safety Study in Subjects with Neutrophilic Asthma
Detailed description
Effect of treatment with navarixin (MK-7123, SCH 527123) on sputum neutrophils and asthma symptoms
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Navarixin | Navarixin 30 mg capsule to be taken by mouth once daily in the morning for 4 weeks. |
| DRUG | Placebo | Placebo capsule to match navarixin to be taken by mouth once daily in the morning for 4 weeks. |
| DRUG | Rescue medication | Participant choice of short-acting beta-2 agonist (salbutamol/albuterol), anticholinergic, or combination medication as needed for asthma symptoms |
Timeline
- Start date
- 2008-05-01
- Primary completion
- 2009-02-01
- Completion
- 2009-02-01
- First posted
- 2008-03-10
- Last updated
- 2019-01-02
- Results posted
- 2014-11-18
Source: ClinicalTrials.gov record NCT00632502. Inclusion in this directory is not an endorsement.