Status:
TERMINATED
Study Comparing the Clinical Efficacy and Health Outcomes of Outpatients With Mild to Moderate Community-Acquired Pneumonia (CAP) Treated With Either Telithromycin Once Daily for 7 Days, or Azithromycin Once Daily for 5 Days
Lead Sponsor:
Sanofi
Conditions:
Pneumonia
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
A multinational, multicenter, randomized, double-blind, study in areas of high pneumococcal resistance comparing the clinical efficacy and health outcomes of outpatients with mild to moderate Communit...
Eligibility Criteria
Inclusion
- Male or female outpatients aged 20 or greater.
- Subjects with a positive Binax NOW S. pneumoniae Urinary Antigen Test and/or positive gram stain for diplococci.
- Subjects with ≤ 7 days of signs and symptoms of CAP.
- Subjects with chest x-ray findings that support a diagnosis of acute pneumonia with presence of a new infiltrate. For subjects with history of chronic obstructive pulmonary disease (COPD), a comparison to previous chest x-ray report is required to confirm the finding of new infiltrates.
- Subjects with diagnosis of acute mild to moderate CAP based on at least one of the following:
- fever (oral \>37.5°C/99.5°F or axillary \>37.4°C/99.4°F or rectal \>38.5°C/101.5°F) or
- elevated total peripheral white blood cell count \>10,000/mm3 or \>15% immature neutrophils (bands), regardless of total peripheral white count and
- new and sudden onset (equal or less than 48 hours) of at least two of the following signs or symptoms:
- cough
- dyspnea or tachypnea (particularly if progressive in nature)
- pleuritic chest pain
- purulent sputum production or change in sputum character
- auscultatory findings (such as rales and/or evidence of pulmonary consolidation)
Exclusion
- Subjects presenting with any of the following will not be included in the study.
- Subjects with CAP requiring hospitalization.
- Subjects with signs and symptoms of severe CAP lasting greater than 7 days.
- Subjects requiring parenteral antibiotic treatment.
- Subjects discharged from hospital within the 10 days before study entry.
- Subjects with visible/gross aspiration pneumonia.
- Subjects with any concomitant pulmonary disease, condition or complication that could confound the interpretation or evaluation of drug efficacy or safety, including:
- severe bronchiectasis, cystic fibrosis or suspected active pulmonary tuberculosis
- suspected acute pulmonary embolism
- emphysema, lung abscess, extra pulmonary extension (e.g., meningitis, septic arthritis, endocarditis)
- known bronchial obstruction or a history of postobstructive pneumonia.
- Subjects with neoplastic lung disease (lung cancer) or another malignancy metastatic to the lungs, and/or requiring chemotherapeutic interventions for this or other neoplasms.
- Subjects with infection requiring administration of other systemic antimicrobial agents.
- Subjects with progressively fatal disease; life expectancy ≤3 months.
- Subjects with myasthenia gravis.
- Subjects with any concomitant condition, including severe and/or uncontrolled cardiovascular, neurologic, endocrine, or other severe and/or uncontrolled major systemic disease that make implementation of the protocol or interpretation of the study results difficult.
- Immunocompromised subjects, such as:
- known HIV subjects with CD4+ T-lymphocyte count dated less than 3 months \<200/mm3 and /or HIV subjects treated with isoniazide or clarithromycin as prophylaxis
- neutropenia (\<1500 neutrophils/mm3) not attributable to the acute infectious disease
- metastatic or hematological malignancy
- splenectomy or known hyposplenia or asplenia
- chronic corticosteroid therapy.
- Subjects with a history of congenital or a family history of long QT syndrome (if not excluded by previous ECG) and subjects with known acquired QT interval prolongation
- Known severe impaired renal function as shown by creatinine clearance \< 30 ml/min either measured or estimated with Cockroft formula.
- Subjects who have received more than 24 hours of effective treatment with other antibiotics, within the 7 days prior to enrollment in the study.
- Subjects with a known or suspected hypersensitivity to, or a known or suspected serious adverse reaction to telithromycin or any macrolide antibiotic.
- Subjects who will require on-study treatment with medications known to have potential drug interactions, including ergot alkaloids derivatives, terfenadine, astemizole, cisapride, pimozide, simvastatin, atorvastatin and lovastatin (see Section 6.2).
- Subjects who have received any investigational drug within 1 month prior to study entry or such treatment is planned for during the study period.
- Subjects who are pregnant or breast-feeding.
- Subjects with recent drug or alcohol abuse.Subjects with a mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study.
- Subject is the investigator or any subinvestigator, research assistance, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the protocol.
- Subjects already enrolled in this study.
Key Trial Info
Start Date :
November 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2006
Estimated Enrollment :
110 Patients enrolled
Trial Details
Trial ID
NCT00237445
Start Date
November 1 2005
End Date
September 1 2006
Last Update
January 11 2011
Active Locations (1)
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1
Sanofi-Aventis
Bridgewater, New Jersey, United States, 08807