Phase 3
N=764
A Study to Evaluate the Efficacy and Safety of Intravenous Ceftaroline Versus Intravenous Ceftriaxone in the Treatment of Adult Hospitalised Patients With Community-Acquired Bacterial Pneumonia in Asia
Community-Acquired Bacterial Pneumonia · Lung Infection of Individual Not Recently Hospitalized
Bottom Line
View on ClinicalTrials.gov: NCT01371838 ↗Enrolled (actual)
764
Serious AEs
7.7%
Results posted
Sep 2014
Primary outcome: Primary: Clinical Cure Rate for Ceftaroline Compared to That for Ceftriaxone at Test of Cure (TOC) in CE Population — 217; 178; 41; 62 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Ceftaroline (Drug); Ceftriaxone (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Pfizer
- Primary completion
- May 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Clinical Cure Rate for Ceftaroline Compared to That for Ceftriaxone at Test of Cure (TOC) in CE Population |
217; 178; 41; 62 | — |
| SECONDARY Clinical Response at End of Treatment (EOT) Visit in MITT Population |
321; 281; 45; 82; 15; 19 | — |
| SECONDARY Clinical Response at End of Treatment (EOT) Visit in CE Population |
222; 186; 36; 54 | — |
| SECONDARY Clinical Response at the Test of Cure (TOC) Visit in MITT Population |
305; 256; 53; 91; 23; 35 | — |
| SECONDARY Clinical Response at the Test of Cure (TOC) Visit in mMITT Population |
68; 67; 9; 21; 3; 8 | — |
| SECONDARY Clinical Response at the Test of Cure (TOC) Visit in ME Population |
50; 47; 7; 15 | — |
| SECONDARY Clinical Response at Test of Cure (TOC) Visit by Pathogen in ME Population |
4; 4; 4; 2; 0; 2 | — |
| SECONDARY Per-Pathogen Microbiological Response at Test of Cure (TOC) Visit by Pathogen in ME Population |
4; 4; 4; 2; 0; 2 | — |
| SECONDARY Per-Patient Microbiological Response at Test of Cure (TOC) Visit in mMITT Population |
68; 67; 9; 21; 3; 8 | — |
| SECONDARY Per-Patient Microbiological Response at Test of Cure (TOC) Visit in ME Population |
50; 47; 7; 15 | — |
| SECONDARY Overall (Clinical and Radiographic) Success Rate at Test of Cure (TOC) Visit in MITT Population |
305; 256; 53; 91; 23; 35 | — |
| SECONDARY Overall (Clinical and Radiographic) Success Rate at Test of Cure (TOC) Visit in CE Population |
217; 178; 41; 62 | — |
| SECONDARY Clinical Relapse at the LFU Visit for Clinical Cure Patients at Test of Cure (TOC) Visit in MITT Population |
286; 244; 7; 5; 12; 7 | — |
| SECONDARY Clinical Relapse at the LFU Visit for Clinical Cure Patients at Test of Cure (TOC) Visit in CE Population |
199; 167; 6; 3; 12; 8 | — |
| SECONDARY Microbiological Re-infection/Recurrence at LFU Visit in mMITT Population |
0; 2; 68; 67; 68; 66 | — |
| SECONDARY Microbiological Re-infection/Recurrence at LFU Visit in ME Population |
0; 1; 50; 47; 50; 46 | — |
Summary
This purpose of this study is to Evaluate the Efficacy and Safety of Intravenous Ceftaroline Versus Intravenous Ceftriaxone in the Treatment of Adult Hospitalised Patients With Community-Acquired Bacterial Pneumonia in Asia.
Eligibility Criteria
Inclusion Criteria
- Males and females 18 or more years of age
- Lung Infection of Individual not Recently Hospitalized meeting the following criteria: Radiographically-confirmed pneumonia (new or progressive infection site of the lungs) consistent with bacterial pneumonia), AND Acute illness (≤ 7 days duration) with at least three of the following clinical signs or symptoms consistent with lung infection: New or increased cough, Purulent sputum or change in sputum character, Auscultatory findings consistent with pneumonia, Difficulty in breathing, short breath, or decreased partial pressure of oxygen in blood, Fever greater than 38ºC oral or body temperature lower than that required for normal body function(< 35ºC), White blood cell count greater than or less than the normal, Greater than 15% immature neutrophils (bands) irrespective of white blood cell count, AND Moderate lung infection
- The subject must require initial hospitalization, or treatment in an emergency room or urgent care setting, by the standard of care
- The subject's infection would require initial treatment with intravenous antimicrobials
- Female subjects of child-bearing potential, and those who are fewer than 2 years post-menopausal, must agree to, and comply with, using highly effective methods of birth control while participating in this study
Exclusion Criteria
- Lung Infection of Individual not Recently Hospitalized suitable for outpatient therapy with an oral antimicrobial agent
- Confirmed or suspected respiratory tract infections attributable to sources other than bacteria from the individuals not recently hospitalized(e.g., ventilator-associated pneumonia, hospital-acquired pneumonia, visible/gross aspiration pneumonia, suspected viral, fungal, or mycobacterial infection of the lung)
- Non-infectious causes of lung lesion (e.g., pulmonary embolism, chemical pneumonitis from aspiration, hypersensitivity pneumonia, congestive heart failure)
- Accumulation of pus in the pleural cavity
- Microbiologically-documented infection with a pathogen known to be resistant to ceftriaxone, or epidemiological or clinical context suggesting high likelihood of a ceftriaxone-resistant "typical" bacterial pathogen.
Data sourced from ClinicalTrials.gov (NCT01371838). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.