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Dose-finding, Pharmacokinetics, and Safety of VABOMERE in Pediatric Subjects With Bacterial Infections

About

Brief Summary

A single dose infusion of Vabomere (meropenem-vaborbactam) is being tested for dose-finding, pharmacokinetics, safety, and tolerability in pediatric subjects from birth to less than 18 years of age with serious bacterial infections

Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase I

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
N/A
Maximum Age
17 Years

Inclusion Criteria:

  • A signed and dated written informed consent from the parent or legal representative and a subject assent (according to local IRB requirements);
  • Male or female from birth to < 18 years of age;
  • Are hospitalized, in stable condition, and receiving systemic antibiotics for a known or suspected bacterial infection; or subjects receiving peri-operative prophylactic use of antibiotics;
  • The subject will be observed in the hospital for at least 6 hours after the study drug is administered;
  • If female and has reached menarche, or has reached Tanner Stage 3 breast development (even if not having reached menarche), the subject is practicing appropriate birth control or is sexually abstinent;
  • Sufficient intravascular access (peripheral or central) to receive study drug.

Subjects will be excluded from the study if any of the following exclusion criteria apply

prior to randomization:

  • Signs of severe sepsis including:
    • Shock or profound hypotension that is not responsive to fluid challenge;
    • Hypothermia (core temperature < 35.6 ºC or 96.1 ºF);
    • Disseminated intravascular coagulation as evidenced by prothrombin time or partial thromboplastin time ≥ 2X the ULN or platelets < 50% of the lower limit of normal;
  • Any surgical or medical condition which, in the opinion of the investigator, would put the subject at increased risk or is likely to interfere with study procedures or PK of the study drug;
  • Females who are of childbearing potential and unwilling to practice abstinence or use at least two methods of contraception (oral contraceptives, barrier methods, approved contraceptive implant) during the entire study period;
  • Female adolescent subjects who are pregnant or breastfeeding or have a positive serum β-hCG pregnancy test at screening and at pre-dose Day 1;
  • Males who are unwilling to practice abstinence or use an acceptable method of broth control during the entire study period (i.e. condom with spermicide);
  • Renal function at screening as estimated by creatinine clearance < 50 mL/min using the Cockcroft-Gault formula;
  • Treatment within 30 days prior to enrollment with valproic acid;
  • Treatment within 30 days prior to enrollment with probenecid;
  • Evidence of significant hepatic disease or dysfunction, including known acute viral hepatitis or hepatic encephalopathy;
  • Neutropenia with absolute neutrophil count (ANC) < 500 cells/mm3;
  • Aspartate aminotransferase or alanine aminotransferase ≥ 3X ULN or total bilirubin ≥ 1.5X ULN;
  • Receipt of any investigational medication or investigational device within 30 days prior to enrollment;
  • Prior exposure to vaborbactam or Vabomere;
  • Use of meropenem within 48 hours of administration of study drug or 12 hours after study drug administration;
  • Known significant hypersensitivity to any beta-lactam antibiotic;
  • Unable or unwilling in the judgment of the Investigator, to comply with the protocol;
  • An employee of the Investigator or study center with direct involvement in the proposed study or other studies under the direction of that Investigator or study center, as well as a family member of the employee or the Investigator;
  • BMI outside the range (below the 5th percentile or above the 95th percentile) for height, age and weight except for children < 2 years of age.)

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Study Stats
Protocol No.
17-000907
Category
Pediatrics
Contact
Elizabeth Lang
Location
  • UCLA Westwood
For Providers
NCT No.
NCT02687906
For detailed technical eligibility, visit ClinicalTrials.gov.