Efficacy and Safety Study of Intravenous to Oral Solithromycin (CEM-101) Compared to Intravenous 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:4/21/2016
Start Date:November 2013
End Date:September 2015

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A Randomized, Double-Blind, Multi-Center Study to Evaluate the Efficacy and Safety of Intravenous to Oral Solithromycin (CEM-101) Compared to Intravenous 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.

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.

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

- Fungal pneumonia

- Pneumocystis jiroveci pneumonia

- Aspiration pneumonia

- Other non-infectious causes of pulmonary infiltrates

- Primary or metastatic lung cancer

- Cystic fibrosis

- Active or suspected tuberculosis

- HIV or myasthenia gravis
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