| Eligibility |
Inclusion Criteria:
Patients who meet all the following diagnostic and clinical criteria are eligible for the
study:
1. Provide written informed consent prior to any study related procedures not part of
normal medical care. Surrogate consent/use of a legally authorized representative may
be provided, if permitted by local country and institution specific guidelines. If a
patient regains consciousness while in the study and, per the Investigator's judgment,
the patient is able to read, assess, understand, and make his/her own decision to
participate in the trial, the patient can agree to continue participation and the
patient should be re consented, if required by local country and institution specific
guidelines.
2. Male or female patients = and < 80 years of age at the time of Informed Consent Form
(ICF) signing with a body mass index (BMI) of < 40 kg/m2 at the time of ICF signing.
3. Hospitalized for = 48 hours, intubated (via endo or nasotracheal tube, including
tracheostomy patients) and receiving mechanical ventilation for = 48 hours at the time
of randomization, and with acute changes made in the ventilator support system to
enhance oxygenation, as determined by arterial blood gas, or worsening PaO2/FiO2
ratio.
4. All patients must have a chest radiograph or a lung CT scan within 48 hours prior to
randomization showing the presence of new or progressive infiltrate(s) suggestive of
bacterial pneumonia (based on Investigator's evaluation).
5. Clinical findings to support diagnosis of VABP. At least 1 of the following must be
documented to be present within 24 hours prior to randomization:
- Documented fever (oral = 38.0 °C [100.4 °F] or a tympanic, temporal, rectal, or
core temperature = 38.3 °C [101.0 °F], axillary or forehead scanner = 37.5 °C
[99.5 °F]) OR
- Hypothermia (rectal/core body temperature = 35.0 °C [95.2 °F]), OR
- Leukocytosis with total peripheral white blood cell count (WBC) = 10 000
cells/mm3, OR
- Leukopenia with total peripheral WBC count = 4500 cells/mm3.
6. Acute Physiology and Chronic Health Evaluation (APACHE II) score between 8 and 30,
inclusive, within 24 hours prior to randomization. Any data collected before ICF
signature as part of a routine standard for patient care (e.g., laboratory values,
Glasgow Coma Score, Acute Physiology Score [APS]) can be used for Screening Visit
assessment, if applicable, without repeating the assessments.
7. High probability of pneumonia due to A. baumannii, defined as follows:
- RDT, performed within 36 hours prior to randomization, using an acceptable
respiratory sample (PBS, BAL, mini BAL, or ETA) positive for A. baumannii, OR
- A surveillance culture from a respiratory sample positive for A. baumannii within
72 hours prior to randomization.
Part B specific:
1. Patients who have been treated previously with an empiric antibiotic regimen and have
failed treatment, both clinically and microbiologically, if they have an identified
CRAB which has been shown to be non-susceptible in vitro to each of the antibiotic(s)
of the empiric antibiotic regimen or has been identified from a culture performed
after at least 48 hours of empiric antibiotic regimen, AND/OR
2. Has an infection caused by A. baumannii organisms known to be resistant to colistin
(defined as MIC = 4 mg/L by a non-agar-based method) based on evidence from culture or
susceptibility testing after at least 48 hours of antibiotic treatment.
Exclusion Criteria:
- Patients who meet any of the following criteria are not eligible to participate in
this study:
1. Known or suspected community acquired bacterial pneumonia or viral, fungal, or
parasitic pneumonia.
2. Sustained shock with persisting hypotension requiring vasopressors to maintain
mean arterial pressure = 60 mmHg
3. Known or suspected allergy to polymyxin, rifabutin, BAT, or their excipients.
4. Any of the following health conditions:
- Confirmed legionella infection (Legionella pneumophila pneumonia),
Aspergillus spp. pneumonia (testing is not required)
- Candida spp. infection requiring systemic treatment
- Cystic fibrosis
- Known or suspected Pneumocystitis jiroveci pneumonia
- Known or suspected active tuberculosis
- Lung abscess
- Solid organ transplant within 6 months prior to randomization
- Pleural empyema
- Evidence of deep seated infection outside the respiratory tract, e.g.,
endocarditis, osteomyelitis.
- Known or suspected neuropathy or neuromuscular disease
- Known HIV infection
5. Bronchial obstruction or a history of post obstructive pneumonia (this does not
exclude patients with pneumonia who have an underlying chronic obstructive
pulmonary disease).
6. Acute graft versus host disease Grade = 3.
7. Expected survival < 72 hours or a Do Not Resuscitate Order.
8. Burns > 40% of total body surface area.
9. Current or anticipated neutropenia with absolute neutrophil count < 1000
cells/mm3.
10. Severe renal disease defined as an estimated creatinine clearance as per
Cockcroft Gault (CLCR CG) < 30 mL/minute or estimated glomerular infiltration
rate (eGFR) as per Modified Diet in Renal Disease (MDRD) equation < 30
mL/min/1.73 m2, or requirement for peritoneal dialysis, hemodialysis,
hemofiltration, or a urine output < 20 mL/hour over a 24 hour period.
11. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline
phosphatase (ALP), or bilirubin (conjugated/unconjugated) = 3 × upper limit of
normal (ULN) values used by the laboratory performing the test or Child Pugh
Class B and C in patients with chronic liver function impairment. Evidence of
significant hepatic disease or dysfunction, including known acute viral
hepatitis, hepatic cirrhosis, hepatic failure, chronic ascites, or hepatic
encephalopathy.
12. Received systemic or inhaled antibiotic therapy potentially effective against A.
baumannii within 72 hours prior to randomization for = 36 hours
13. Investigator's opinion of clinically significant electrocardiogram (ECG) finding
such as new ischemic changes, infarct, or ventricular arrhythmia with immediate
potential for a fatal outcome, bradycardia not corrected by pacemaker or
medication, or, prior to the current infection, a history of New York Heart
Association (NYHA) Class IV cardiac failure defined as severe limitations -
experiences symptoms even while at rest, mostly bedbound patients, within 1 year.
14. Abnormal QT interval corrected by Fridericia (QTcF): > 450 ms confirmed with
repeat ECG.
15. Stroke (ischemic or intracerebral hemorrhage) within 5 days prior to
randomization.
16. Women who are pregnant or nursing, or who are of childbearing potential and
unwilling to use an acceptable method of birth control (e.g., intra-uterine
device [IUD], male partner sterilization, or complete sexual abstinence) for at
least 30 days after the last dose of the study drug. Negative pregnancy test
should be obtained before randomization. The following women are not considered
to have childbearing potential: 1) those who have undergone surgical
sterilization, including hysterectomy and/or bilateral oophorectomy and/or
bilateral salpingectomy, but excluding bilateral tubal occlusion; 2) age = 50 and
post-menopausal as defined by amenorrhea for 12 months or more following
cessation of all exogenous hormonal treatments.
17. Male patients with female partners of childbearing potential who are unwilling to
use 2 methods of contraception, one of which must be a barrier method (e.g.,
condom), for at least 30 days after the last dose of study drug.
18. Previous exposure to BV100.
19. Patients who are currently enrolled in or have not yet completed at least 30 days
since ending another investigational device or drug trial or are receiving other
investigational agents.
20. Not willing to comply with all study procedures.
21. Confirmed or suspected severe acute respiratory syndrome coronavirus 2
(SARS-CoV-2) infection based on local standard-of-care assessments available
during Screening, unless the suspected A. baumannii pneumonia is diagnosed 14
days or more after the detection of SARS CoV 2.
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