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Phase 1 N=35 Basic Science

Safety and Tolerability of Ceftazidime-Avibactam for Pediatric Patients With Suspected or Confirmed Infections

Systemic Infections

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

OutcomeResultp-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).
View full record on ClinicalTrials.gov →

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.

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