Clinical Study of S-649266 for the Treatment of Nosocomial Pneumonia Caused by Gram-negative Pathogens
Status: | Completed |
---|---|
Conditions: | Pneumonia, Pneumonia |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/6/2019 |
Start Date: | October 24, 2017 |
End Date: | April 1, 2019 |
A Multicenter, Randomized, Double-blind, Parallel-group, Clinical Study of S-649266 Compared With Meropenem for the Treatment of Hospital-acquired Bacterial Pneumonia, Ventilator-associated Bacterial Pneumonia, or Healthcare-associated Bacterial Pneumonia Caused by Gram-negative Pathogens
To compare all-cause mortality at Day 14 in participants receiving S-649266 with participants
receiving the comparator, meropenem, in adults with hospital-acquired bacterial pneumonia
(HABP), ventilator-associated bacterial pneumonia (VABP), or healthcare-associated bacterial
pneumonia (HCABP) caused by Gram-negative pathogens.
receiving the comparator, meropenem, in adults with hospital-acquired bacterial pneumonia
(HABP), ventilator-associated bacterial pneumonia (VABP), or healthcare-associated bacterial
pneumonia (HCABP) caused by Gram-negative pathogens.
Inclusion Criteria:
- Subjects 18 years or older at the time of signing informed consent
- Subjects who have provided written informed consent or their informed consent has been
provided by a legally authorized representative
- Subjects who meet the clinical diagnosis criteria for hospital-acquired bacterial
pneumonia (HABP),ventilator-associated bacterial pneumonia (VABP), or
healthcare-associated bacterial pneumonia (HCABP)
- All subjects must fulfill at least 1 of the following clinical criteria at screening:
1. New onset or worsening of pulmonary symptoms or signs, such as cough, dyspnea,
tachypnea (eg, respiratory rate > 25 breaths/minute), expectorated sputum
production, or requirement for mechanical ventilation
2. Hypoxemia (eg, a partial pressure of oxygen [PaO2] < 60 mm Hg while the subject
is breathing room air, as determined by arterial blood gas [ABG], or worsening of
the ratio of the PaO2 to the fraction of inspired oxygen [PaO2/FiO2])
3. Need for acute changes in the ventilator support system to enhance oxygenation,
as determined by worsening oxygenation (ABG or PaO2/FiO2) or needed changes in
the amount of positive end-expiratory pressure
4. New onset of or increase in (quantity or characteristics) suctioned respiratory
secretions, demonstrating evidence of inflammation and absence of contamination
- All subjects must have at least 1 of the following signs:
1. Documented fever (ie, core body temperature [tympanic, rectal, esophageal] ≥ 38°C
[100.4°F], oral temperature ≥ 37.5°C, or axillary temperature ≥ 37°C)
2. Hypothermia (ie, core body temperature [tympanic, rectal, esophageal] ≤ 35°C
[95.0°F], oral temperature ≤ 35.5°C and axillary temperature ≤ 36°C)
3. Leukocytosis with a total peripheral white blood cell (WBC) count ≥ 10,000
cells/mm³
4. Leukopenia with total peripheral WBC count ≤ 4500 cells/mm³
5. Greater than 15% immature neutrophils (bands) noted on peripheral blood smear
- All subjects must have a chest radiograph during screening showing the presence of new
or progressive infiltrate(s) suggestive of bacterial pneumonia. A computed tomography
(CT) scan in the same time window showing the same findings could also be acceptable
- All subjects must have a suspected Gram-negative infection involving the lower
respiratory tract
Exclusion Criteria:
- Subjects who have known or suspected community-acquired bacterial pneumonia (CABP),
atypical pneumonia, viral pneumonia, or chemical pneumonia (including aspiration of
gastric contents, inhalation injury)
- Other exclusions based on the prescribing information of meropenem or linezolid, prior
antibiotic usage, age, and pregnancy.
We found this trial at
16
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