Safety and Efficacy of Solithromycin in Adolescents and Children With Community-Acquired Bacterial Pneumonia
Status: | Terminated |
---|---|
Conditions: | Pneumonia |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | Any - 17 |
Updated: | 1/5/2019 |
Start Date: | April 2016 |
End Date: | March 21, 2018 |
A Phase 2/3, Randomized, Open-Label, Multi-center Study to Determine the Safety and Efficacy of Solithromycin in Adolescents and Children With Suspected or Confirmed Community-Acquired Bacterial Pneumonia
This is a phase 2/3, randomized, open-label, active control, multi-center study to assess the
safety and efficacy of solithromycin in children and adolescents with community-acquired
bacterial pneumonia (CABP).
safety and efficacy of solithromycin in children and adolescents with community-acquired
bacterial pneumonia (CABP).
Subjects who meet all inclusion/exclusion criteria and sign the informed consent/assent were
enrolled. Subjects were randomized to receive solithromycin or a comparator antibiotic,
administered IV and/or by mouth (PO) based on weight and age. Subjects were treated daily for
5 to 7 days with oral solithromycin and 5 to 7 days with IV or IV-to-oral solithromycin.
Subjects were treated for 5 to 10 days with comparator antibiotics. Subjects received safety
and efficacy assessments during and after treatment.
enrolled. Subjects were randomized to receive solithromycin or a comparator antibiotic,
administered IV and/or by mouth (PO) based on weight and age. Subjects were treated daily for
5 to 7 days with oral solithromycin and 5 to 7 days with IV or IV-to-oral solithromycin.
Subjects were treated for 5 to 10 days with comparator antibiotics. Subjects received safety
and efficacy assessments during and after treatment.
Inclusion Criteria:
- History of and/or documented fever (rectal, ear, or oral temperature ≥38°C or axillary
temperature ≥37.5°C) or hypothermia (rectal, ear, or oral temperature <35°C or
axillary temperature <34.5°C)
- Chest radiograph infiltrates consistent with bacterial pneumonia (or pneumonia caused
by atypical bacterial agents); if a subject is outpatient and starting on oral
therapy, a radiograph is not required.
- Presence of at least 2 of the following signs or symptoms:
- Cough
- Difficulty breathing
- Production of purulent sputum
- Chest pain
- Grunting
- Hypotension
- Tachycardia, defined as follows:
2 months to <24 months: ≥160 beats/min 24 months to <10 years: ≥140 beats/min
- 10 years: ≥100 beats/min
- Tachypnea, defined as follows:
2 months to <12 months: ≥50 breaths/min 12 months to <5 years: ≥40 breaths/min
- 5 years: ≥20 breaths/min
- Physical exam consistent with pulmonary consolidation
- Presence of at least 1 of the following:
- Leukocytosis (≥12,000 white blood cells [WBC]/mm3)
- Leukopenia (<5000 WBC/mm3)
- ≥10% immature neutrophils (bands) regardless of total peripheral WBC
- Elevated inflammatory markers (C-reactive protein or procalcitonin)
- Oxygen saturation <97% on room air
- Organism consistent with a typical respiratory pathogen identified
Exclusion Criteria:
- Ventilator-associated or hospital-acquired pneumonia
- >48 hours of systemic antibacterial therapy
- confirmed or suspected bacterial meningitis
- breast-feeding females
- positive pregnancy test
We found this trial at
22
sites
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