Study of Cidecin™ (Daptomycin) to Rocephin® (Ceftriaxone) in the Treatment of Moderate to Severe Community-Acquired Acute Bacterial Pneumonia Due to S. Pneumoniae
This study has been completed.
Information provided by (Responsible Party):
Cubist Pharmaceuticals LLC
First received: October 4, 2007
Last updated: July 16, 2015
Last verified: October 2007
A COMPARASON OF CIDECIN™ (DAPTOMYCIN) TO ROCEPHIN® (CEFTRIAXONE) IN THE TREATMENT OF MODERATE TO SEVERE COMMUNITY-ACQUIRED ACUTE BACTERIAL PNEUMONIA DUE TO S. PNEUMONIAE
Intervention Model: Parallel Assignment
| Study Start Date:
| Study Completion Date:
| Primary Completion Date:
||February 2002 (Final data collection date for primary outcome measure)
|Ages Eligible for Study:
||18 Years and older (Adult, Senior)
|Sexes Eligible for Study:
- Provide signed and dated informed consent.
- Adults, 18 years of age or older of either gender and of any race weighing up to 150 kg. Female patients of childbearing potential MUST be nonpregnant (confirmed by negative serum pregnancy test), nonlactating, and must be willing to practice reliable birth control measures during and for at least 30 days after treatment with study drug(s).
- Have a new pulmonary infiltrate on chest radiograph.
Exhibit at least two of the following clinical symptoms of pneumonia on history or physical:
- Production of purulent sputum or change in character of sputum
- Auscultatory findings on pulmonary examination of rales and/or evidence of pulmonary consolidation (dullness to percussion, bronchial breath sounds, or egophony)
- Dyspnea or tachypnea
- Documented fever, defined as body temperature >38.0 ºC (100.4 ºF) taken orally; >38.5 ºC (101.2 ºF) tympanically; or >39.0 ºC (102.2 ºF) rectally or hypothermia, defined as core body temperature of <35.0 ºC (95.0 ºF)
- An elevated total peripheral white blood cell count (WBC >10,000/mm3); or >15% immature neutrophils (bands), regardless of total peripheral white count; or leukopenia with total WBC <4500/mm3.
- Hypoxemia with a PO2 < 60 mmHg (on room air) or O2 saturation <90% on room air
- Pneumonia which requires hospitalization and intravenous therapy for at least 5 days.
- Willingness to participate in this study and to complete all follow-up assessments.
- Patients with Grade V pneumonia (based on Fine Score; Attachment 8).
- Patients in respiratory failure or incipient respiratory failure if the patient is not a candidate for mechanical ventilation (for any reason).
Any of the following pulmonary conditions that may preclude interpretation of study results:
- Cystic fibrosis
- Primary lung cancer or another malignancy metastatic to the lungs
- Known bronchial obstruction or a history of post-obstructive pneumonia
- Known or suspected active tuberculosis.
- Severe shock (systolic blood pressure <90 mm Hg for >30 minutes not corrected by fluid bolus).
- Clinical evidence of bacterial meningitis (based on lumbar puncture results).
- Severe renal impairment (calculated creatinine clearance <30 mL/min).
- Moribund clinical condition: high likelihood of death during the first 48 hours.
- If HIV positive, known CD4 counts <200/mm3 or evidence of Pneumocystis carinii pneumonia.
- Inability to tolerate ceftriaxone or history of allergy to beta-lactam antibiotics (history of rash alone will not exclude a patient).
- Any individual previously treated with a potentially effective anti-infective agent for > 24 hours (or one dosing day) within 72 hours of enrollment, or prior treatment with any investigational drug (including experimental biologic agents) in previous 30 days or prior therapy with daptomycin.
- Patients who must continue HMG-CoA reductase inhibitor therapy (e.g., simvastatin, lovastatin, etc.) during the study treatment period.
- Anticipation that a second non-protocol systemic antibiotic will be required.
- Induction chemotherapy within 2 weeks prior to enrollment (or exogenous therapies which are anticipated to result in PMN counts of <200 mm3 during Treatment Phase), or patients with severe neutropenia (<200 PMN cells/mm3).
- Patients considered unreliable to return for visits or to comply with study procedures.
- Progressive neoplastic disease (Note: patients with malignancies in remission are eligible).
- Women who are pregnant or nursing/lactating.
- Patients presenting with nosocomial pneumonia (i.e., <14 days after discharge from a skilled nursing facility or hospital with an initial hospitalization of >=3 days duration).
- Clinical suspicion of Legionella pneumonia.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
No Contacts or Locations Provided
||Cubist Pharmaceuticals LLC
History of Changes
|Other Study ID Numbers:
|Study First Received:
||October 4, 2007
||July 16, 2015
Keywords provided by Cubist Pharmaceuticals LLC:
Moderate to Severe Community-Acquired Acute Bacterial Pneumonia Due to S. Pneumoniae
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on July 24, 2017
Respiratory Tract Diseases
Respiratory Tract Infections