Trials / Terminated
TerminatedNCT00288223
Telithromycin in Acute Exacerbation of Chronic Bronchitis
Multicenter Non Comparative Phase IV Study on the Safety and Efficacy of Telithromycin 800 mg Per Day for 5 Days in the Treatment of Acute Exacerbation of Chronic Bronchitis in Adults
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 54 (actual)
- Sponsor
- Sanofi · Industry
- Sex
- All
- Age
- 35 Years
- Healthy volunteers
- Not accepted
Summary
Study objectives: * to document the clinical efficacy of telithromycin(800 mg per day for 5 days) at Test Of the Cure (TOC)visit (D12-D19), in acute exacerbation of chronic bronchitis. * to assess the long-term clinical efficacy of telithromycin by telephone at D25-D35 (V3) * to assess the safety of telithromycin
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Telithromycin | one daily intake of 800 mg (i.e. 2 x 400 mg tablets) per os in a single intake with a meal for 5 days. |
Timeline
- Start date
- 2006-01-01
- Primary completion
- 2007-01-01
- Completion
- 2007-01-01
- First posted
- 2006-02-07
- Last updated
- 2009-12-09
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT00288223. Inclusion in this directory is not an endorsement.