Phase 1
N=35
Safety and Tolerability of Ceftazidime-Avibactam for Pediatric Patients With Suspected or Confirmed Infections
Systemic Infections
Bottom Line
View on ClinicalTrials.gov: NCT01893346 ↗Enrolled (actual)
35
Serious AEs
0.0%
Results posted
May 2015
Primary outcome: Primary: Pharmacokinetic Parameters of Avibactam and Ceftazidime for Cohort 1 and 2: AUC — 35140; 219100; 33590; 212400 h*ng/mL
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 1
- Interventions
- CAZ-AVI (Drug)
- Age
- Pediatric · 0+ yrs
- Sex
- All
- Sponsor
- Pfizer
- Primary completion
- Oct 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pharmacokinetic Parameters of Avibactam and Ceftazidime for Cohort 1 and 2: AUC |
35140; 219100; 33590; 212400; 36250; 229200 | — |
| PRIMARY Pharmacokinetic Parameters of Avibactam and Ceftazidime for Cohort 1 and 2: Cmax |
15090; 79750; 14140; 81270 | — |
Summary
To assess the pharmacokinetics, safety and tolerability of a single dose of CAZ-AVI in children from 3 months of age to <18 years.
Eligibility Criteria
Inclusion Criteria
- Written informed consent will be obtained from parent(s) or other legally acceptable representative(s), and informed assent from patient (if age appropriate) will be obtained
- Male or female children ages ≥3 months to <18 years.
- Hospitalized, receiving systemic antibiotic therapy for the treatment of a suspected or confirmed infection, and expected to require hospitalization until after the end of treatment (EOT) evaluations are completed.
- If female and has reached menarche, or has reached Tanner stage 3 breast development (even if not having reached menarche), the patient is practicing appropriate birth control or is sexually abstinent.
- Likely to survive the current illness or hospitalization.
- Sufficient intravascular access (peripheral or central) to receive study drug.
Exclusion Criteria
- History of hypersensitivity reactions to carbapenems, cephalosporins, penicillin, other β-lactam antibiotics.
- If female, currently pregnant or breast feeding or has a positive serum β-human chorionic gonadotropin (β-hCG) pregnancy test.
- Receipt of a blood or blood component (e.g., red blood cells, fresh frozen plasma, platelets) transfusion during the 24-hour period before enrolment.
- BMI outside the range (below the 5th percentile or above the 85th percentile) for height, age, and weight except for children <2 years of age.
- Babies born prior to 37 weeks gestation (cohort 4 only).
Data sourced from ClinicalTrials.gov (NCT01893346). 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.