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

In the current era of increased resistance to extended spectrum cephalosporins, carbapenem
antimicrobial agents are frequently the antibiotics of "last defense" for the most resistant
pathogens in serious infections, including those found in complicated Urinary Tract
Infections (cUTI). The recent dissemination of serine carbapenemases (e.g. KPC) in
Enterobacteriaceae in many hospitals worldwide now poses a considerable threat to the
carbapenems and other members of the beta-lactam class of antimicrobial agents.

Rempex developed meropenem-vaborbactam administered as a fixed combination by IV infusion, to
treat serious Gram-negative infections, such as cUTIs, including those infections caused by
bacteria resistant to currently available carbapenems.

This study is an open label, dose-finding, pharmacokinetics, safety, and tolerability study
of a single dose infusion of meropenem-vaborbactam in pediatric subjects from birth to less
than 18 years of age with serious bacterial infections

Inclusion Criteria:

1. A signed and dated written informed consent from the parent or legal representative
and a subject assent (according to local IRB requirements);

2. Male or female from birth to < 18 years of age;

3. 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;

4. The subject will be observed in the hospital for at least 6 hours after the study drug
is administered;

5. 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;

6. 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:

1. Signs of severe sepsis including:

1. Shock or profound hypotension that is not responsive to fluid challenge;

2. Hypothermia (core temperature < 35.6 ºC or 96.1 ºF);

3. Disseminated intravascular coagulation as evidenced by prothrombin time or
partial thromboplastin time ≥ 2X the ULN or platelets < 50% of the lower limit of
normal;

2. 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;

3. 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;

4. 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;

5. 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);

6. Renal function at screening as estimated by creatinine clearance < 50 mL/min using the
Cockcroft-Gault formula;

7. Treatment within 30 days prior to enrollment with valproic acid;

8. Treatment within 30 days prior to enrollment with probenecid;

9. Evidence of significant hepatic disease or dysfunction, including known acute viral
hepatitis or hepatic encephalopathy;

10. Neutropenia with absolute neutrophil count (ANC) < 500 cells/mm3;

11. Aspartate aminotransferase or alanine aminotransferase ≥ 3X ULN or total bilirubin ≥
1.5X ULN;

12. Receipt of any investigational medication or investigational device within 30 days
prior to enrollment;

13. Prior exposure to vaborbactam or Vabomere;

14. Use of meropenem within 48 hours of administration of study drug or 12 hours after
study drug administration;

15. Known significant hypersensitivity to any beta-lactam antibiotic;

16. Unable or unwilling in the judgment of the Investigator, to comply with the protocol;

17. 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;

18. 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.)