Efficacy and Safety Study of Oral Solithromycin (CEM-101) Compared to Oral Moxifloxacin in Treatment of Patients With Community-Acquired Bacterial Pneumonia
Status: | Completed |
---|---|
Conditions: | Pneumonia |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/8/2014 |
Start Date: | December 2012 |
End Date: | July 2014 |
Contact: | Kay Clark, RN |
Email: | kclark@cempra.com |
A Randomized, Double-Blind, Multi-Center Study to Evaluate the Efficacy and Safety of Oral Solithromycin (CEM-101) Compared to Oral Moxifloxacin in the Treatment of Adult Patients With Community-Acquired Bacterial Pneumonia
This study will evaluate the safety and efficacy of an experimental antibiotic,
solithromycin, in the treatment of adult patients with community-acquired pneumonia.
solithromycin, in the treatment of adult patients with community-acquired pneumonia.
Community-acquired bacterial pneumonia (CABP) is an acute infection of the pulmonary
parenchyma with symptoms such as fever or hypothermia, chills, rigors, chest pain, and/or
dyspnea. The widespread emergence of antibiotic resistant pathogens, including the
macrolide-resistant Streptococcus pneumoniae, has resulted in a need for new and effective
antibiotics that have activity against CABP pathogens. Solithromycin is a fourth generation
macrolide antibiotic with excellent activity against resistant S. pneumoniae and other key
typical and atypical bacterial respiratory pathogens. A completed Phase 2 study showed
comparable efficacy to levofloxacin in adults with CABP.
parenchyma with symptoms such as fever or hypothermia, chills, rigors, chest pain, and/or
dyspnea. The widespread emergence of antibiotic resistant pathogens, including the
macrolide-resistant Streptococcus pneumoniae, has resulted in a need for new and effective
antibiotics that have activity against CABP pathogens. Solithromycin is a fourth generation
macrolide antibiotic with excellent activity against resistant S. pneumoniae and other key
typical and atypical bacterial respiratory pathogens. A completed Phase 2 study showed
comparable efficacy to levofloxacin in adults with CABP.
Inclusion Criteria:
- Male and female patients ≥ 18 years of age
- An acute onset of at least 3 of the following signs and symptoms (new or worsening):
1. Cough
2. Production of purulent sputum
3. Shortness of breath (dyspnea)
4. Chest pain due to pneumonia
- At least 1 of the following:
1. Fever
2. Hypothermia
3. Presence of pulmonary rales and/or evidence of pulmonary consolidation
- PORT Risk Class II, III, or IV
- Presence of lobar, multilobar, or patchy parenchymal infiltrate(s) consistent with
acute bacterial pneumonia on a pulmonary imaging study
- Not received any systemic antibiotics during the prior 7 days
Exclusion Criteria:
- Ventilator-associated pneumonia
- Known anatomical or pathological bronchial obstruction or a history of bronchiectasis
or documented severe chronic obstructive pulmonary disease
- Hospitalization within 90 days or residence in a long-term care facility within 30
days prior to the onset of symptoms
- Presence of known:
1. Viral or fungal pneumonia
2. Pneumocystis jiroveci pneumonia
3. Aspiration pneumonia
4. Other non-infectious causes of pulmonary infiltrates (e.g. pulmonary embolism,
hypersensitivity pneumonia, congestive heart failure)
5. Primary or metastatic lung cancer
6. Cystic fibrosis
7. Active or suspected tuberculosis
- Known HIV or myasthesia gravis
We found this trial at
26
sites
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