MAD Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Intravenous Zidebactam in Healthy Adults

A double-blind, placebo-controlled study where healthy adult subjects will be randomly
assigned to receive either of the investigational products (Zidebactam or placebo) in 2
multiple ascending dose (MAD) cohorts.

Primary Objective: to evaluate the safety and tolerability of multiple escalating doses of
intravenous (IV) zidebactam in healthy adult human subjects.

Secondary Objective: to evaluate the pharmacokinetics (PK) of multiple escalating doses of
IV zidebactam in healthy adult human subjects.

Inclusion Criteria:

1. Have a body mass index of 18 to 30 kg/m2 (both inclusive) calculated as weight
(kg)/height (m2).

2. Medical history without any major pathology/surgery in the last 6 months prior to
screening.

3. All values of hematology, serum chemistry, coagulation, and urinalysis showing no
clinically significant deviations from normal as judged by the Principal
Investigator.

4. Resting supine blood pressure of 90 to 139 (systolic)/40 to 89 (diastolic) mmHg and a
resting pulse rate of 40 to 100 beats per minute.

5. Calculated creatinine clearance ≥80 mL/min (Cockcroft-Gault method).

6. Computerized 12-lead ECG recording without signs of clinically significant pathology
and showing no clinically significant deviation as judged by the Principal
Investigator.

Exclusion Criteria:

1. History of clinically significant food or drug allergy, including known
hypersensitivity to β lactam drugs or other related drugs.

2. History of Clostridium difficile induced diarrhea or infection within 1 year before
screening

3. Consumed more than 28 units of alcohol per week at any time in the 6 months before
investigational product administration

4. History/evidence of clinically relevant pathology related to the cardiovascular
system, central nervous system, respiratory tract, gastrointestinal tract,
endocrinology, immunology, hematology or any other systemic disorder/major surgeries,
that in the opinion of the Principal Investigator would confound the subject's
participation and follow-up in the study.