Study of Single Dose Daptomycin in Pediatric Patients With Gram-positive Infection for Which They Are Receiving Standard Antibiotics
Status: | Completed |
---|---|
Conditions: | Infectious Disease, Infectious Disease |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 2 - 17 |
Updated: | 12/22/2017 |
Start Date: | August 24, 2005 |
End Date: | August 9, 2006 |
An Evaluation of the Pharmacokinetics of a Single Dose of Daptomycin (4 mg/kg) in Pediatric Patients Aged Two to Seventeen Years Who Are Concurrently Receiving Standard Antibiotic Therapy for Proven or Suspected Gram-positive Infection
The purpose of this study is to evaluate the pharmacokinetics of a single dose of daptomycin
in patients aged 2-17 years old who have a suspected or proven gram-positive infection for
which they are receiving standard antibiotic therapy. The tolerability of a single dose of
daptomycin in these patients will also be assessed.
in patients aged 2-17 years old who have a suspected or proven gram-positive infection for
which they are receiving standard antibiotic therapy. The tolerability of a single dose of
daptomycin in these patients will also be assessed.
Inclusion Criteria:
- 2-17 years old
- Suspected or diagnosed gram-positive infection for which the patient is receiving
standard antibiotic therapy
- Clinically stable with no evidence of hemodynamic instability in the 72 hour window
prior to enrollment, and no history or evidence of renal or hepatic compromise, or
clinically significant alterations in fluid/electrolyte homeostasis
- Creatinine clearance (CLcr) ≥ 80 ml/min/1.73 m2 as determined by the Schwartz equation
- Creatine phosphokinase (CPK) levels within normal limits
Exclusion Criteria:
- Known allergy to daptomycin
- History of clinically significant cardiovascular, renal, hepatic, pulmonary
(well-controlled asthma is acceptable), gastrointestinal, endocrine, hematologic, or
autoimmune disease
- Pneumonia as sole gram-positive infection
- Use of HMG-CoA reductase inhibitors or other systemic anti-hyperlipidemic agents
within 7 days prior to study drug administration and expected use through 3 days
post-dose
- Clinically significant abnormal laboratory test results (including electrocardiograms
[ECGs]), as determined by Investigator
- Body mass index (BMI) that is outside of the 5th to 95th percentile for age
- History (personal or 1st degree relative) of clinically significant muscular disease,
nervous system, seizure or psychiatric disorder
- Expected intramuscular (IM) injection within 3 days following dosing
- Expected surgical procedure(s) within 3 days following dosing
- Unexplained muscular weakness
- Rhabdomyolysis, myositis or septic shock
We found this trial at
3
sites
529 West Markham Street
Little Rock, Arkansas 72205
Little Rock, Arkansas 72205
(501) 686-7000
University of Arkansas for Medical Sciences The University of Arkansas for Medical Sciences (UAMS) in...
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