Study Comparing the Safety and Efficacy of Intravenous CXA-201 and Intravenous Levofloxacin in Complicated Urinary Tract Infection, Including Pyelonephritis

Approximately 500 subjects will be enrolled into this study and randomized 1:1 to receive
CXA-201 or comparator (levofloxacin) resulting in 250 subjects per treatment arm. Subject
participation will require a minimum commitment of 35 days and a maximum of 42 days. Subjects
will be hospitalized for the administration of all doses of IV study therapy. A test of cure
visit will occur at 7 days after the last dose of study drug and a late follow-up evaluation
or contact will occur a minimum of 28 days and a maximum of 35 days after the last dose of
study drug.

Inclusion Criteria:

1. Provide written informed consent prior to any study-related procedure not part of
normal medical care (a legally acceptable representative may provide consent if the
subject is unable to do so, provided this is approved by local country and institution
specific guidelines).

2. Be males or females ≥ 18 years of age

3. If female, subject is non-lactating, and is either:

1. Not of childbearing potential, defined as postmenopausal for at least 1 year or
surgically sterile due to bilateral tubal ligation, bilateral oophorectomy, or
hysterectomy; or

2. Of childbearing potential and is practicing a barrier method of birth control
(e.g., a diaphragm or contraceptive sponge) along with 1 of the following
methods: oral or parenteral contraceptives (for 3 months prior to study drug
administration), or a vasectomized partner. Or, subject is practicing abstinence
from sexual intercourse. Subjects must be willing to practice these methods for
the duration of the trial and for at least 35 days after last dose of study
medication.

4. Males are required to practice reliable birth control methods (condom or other barrier
device) during the conduct of the study and for at least 35 days after last dose of
study medication.

5. Pyuria (white blood cell [WBC] count > 10/μL in unspun urine or ≥ 10 per high power
field in spun urine).

6. Clinical signs and/or symptoms of cUTI, either of:

1. Pyelonephritis, as indicated by at least 2 of the following:

- Documented fever (oral temperature > 38°C) accompanied by patient symptoms
of rigors, chills, or "warmth";

- Flank pain;

- Costovertebral angle tenderness or suprapubic tenderness on physical exam;
or

- nausea or vomiting; OR

2. Complicated lower UTI, as indicated by at least 2 of the following:

- At least 2 of the following new or worsening symptoms of cUTI:

- Dysuria; urinary frequency or urinary urgency;

- Documented fever (oral temperature > 38°C) accompanied by patient
symptoms of rigors, chills, or "warmth";

- Suprapubic pain or flank pain;

- Costovertebral angle tenderness or suprapubic tenderness on physical
exam; or

- Nausea or vomiting; plus,

- At least 1 of the following complicating factors:

- Males with documented history of urinary retention;

- Indwelling urinary catheter that is scheduled to be removed during IV
study therapy and before the EOT;

- Current obstructive uropathy that is scheduled to be medically or
surgically relieved during IV study therapy and before the EOT; or

- Any functional or anatomical abnormality of the urogenital tract
(including anatomic malformations or neurogenic bladder) with voiding
disturbance resulting in at least 100 mL residual urine.

7. Have a pretreatment baseline urine culture specimen obtained within 24 hours before
the start of administration of the first dose of study drug.

NOTE: Subjects may be enrolled in this study and start IV study drug therapy before
the Investigator knows the results of the baseline urine culture.

8. Require IV antibacterial therapy for the treatment of the presumed cUTI.

Exclusion Criteria:

1. Have a documented history of any moderate or severe hypersensitivity or allergic
reaction to any β-lactam or quinilone antibacterial (Note: for β-lactams, a history of
a mild rash followed by uneventful re-exposure is not a contraindication to
enrollment)

2. Have a concomitant infection at the time of randomization, which requires non-study
systemic antibacterial therapy in addition to IV study drug therapy. (Drugs with only
gram-positive activity [e.g., vancomycin, linezolid] are allowed.)

3. Receipt of any amount of potentially therapeutic antibacterial therapy after
collection of the pretreatment baseline urine culture and before administration of the
first dose of study drug.

4. Receipt of any dose of a potentially therapeutic antibacterial agent for the treatment
of the current UTI within 48 hours before the study-qualifying pretreatment baseline
urine is obtained (exceptions: subjects with an active cUTI who have received prior
antibiotics may be enrolled provided a minimum of 48 hours have elapsed between the
last dose of the prior antibiotic and the time of obtaining the baseline urine
specimen. Subjects receiving current antibiotic prophylaxis for cUTI who present with
signs and symptoms consistent with an active new cUTI may be enrolled provided all
other eligibility criteria are met including obtaining a pre-treatment qualifying
baseline urine culture).

5. Intractable urinary infection at baseline that the Investigator anticipates would
require more than 7 days of study drug therapy.

6. Complete, permanent obstruction of the urinary tract.

7. Confirmed fungal urinary tract infection at time of randomization (with ≥ 103 fungal
CFU/mL).

8. Permanent indwelling bladder catheter or urinary stent including nephrostomy.

9. Suspected or confirmed perinephric or intrarenal abscess.

10. Suspected or confirmed prostatitis.

11. Ileal loop or known vesico-ureteral reflux.

12. Severe impairment of renal function including an estimated CrCl < 30 mL/min,
requirement for peritoneal dialysis, hemodialysis or hemofiltration, or oliguria (< 20
mL/h urine output over 24 hours).

13. Current urinary catheter that is not scheduled to be removed before the EOT
(intermittent straight catheterization during the IV study drug administration period
is acceptable).

14. Any condition or circumstance that, in the opinion of the Investigator, would
compromise the safety of the subject or the quality of study data.

15. Any rapidly progressing disease or immediately life-threatening illness including
acute hepatic failure, respiratory failure, and septic shock.

16. Immunocompromising condition, including established AIDS, hematological malignancy, or
bone marrow transplantation, or immunosuppressive therapy including cancer
chemotherapy, medications for prevention of organ transplantation rejection, or the
administration of corticosteroids equivalent to or greater than 40 mg of prednisone
per day administered continuously for more than 14 days preceding randomization.

17. One or more of the following laboratory abnormalities in baseline specimens: aspartate
aminotransferase (AST [SGOT]), alanine aminotransferase (ALT [SGPT]), alkaline
phosphatase, or total bilirubin level greater than 3 times the upper limit of normal
(ULN), absolute neutrophil count less than 500/μL, platelet count less than 40,000/μL,
or hematocrit less than 20%.

18. Participation in any clinical study of an investigational product within 30 days prior
to the proposed first day of study drug.

19. Previous participation in any study of CXA-101 or CXA-201.

20. Women who are pregnant or nursing.