Clinical Trials Directory

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

TypeNameDescription
DRUGTelithromycinone 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.

Telithromycin in Acute Exacerbation of Chronic Bronchitis (NCT00288223) · Clinical Trials Directory