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• Register: EUCTR
• Last refreshed on: 10 December 2019
• Main ID: EUCTR2012-002862-11-PT
• Date of registration: 21/08/2015
• Prospective Registration: Yes
• Primary sponsor: Cubist Pharmaceuticals LLC, an indirect wholly-owned subsidiary of Merck Sharp & Dohme Corp.
• Public title: -
• Scientific title: A Prospective, Randomized, Double-Blind, Multicenter, Phase 3 Study to Assess the Safety and Efficacy of Intravenous Ceftolozane/tazobactam Compared With Meropenem in Adult Patients with Ventilated Nosocomial Pneumonia (VNP) - Assessment of the Safety Profile and Efficacy of Ceftolozane/Tazobactam in Nosocomial Pneumonia
• Date of first enrolment: 06/10/2015
• Target sample size: 726
• Recruitment status: Not Recruiting
• URL: https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2012-002862-11
• Study type: Interventional clinical trial of medicinal product
• Study design: Controlled: yes; Randomised: yes; Open: no; Single blind: no; Double blind: yes; Parallel group: yes; Cross over: no; Other: no; If controlled, specify comparator, Other Medicinial Product: yes; Placebo: no; Other: no; Number of treatment arms in the trial: 2
• Phase: Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no

Countries of recruitment

Australia, Austria, Belgium, Brazil, Canada, China, Colombia, Croatia, Czech Republic, Estonia, France, Georgia, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Israel, Italy, Korea, Republic of, Latvia, Netherlands, New Zealand, Philippines, Portugal, Russian Federation, Singapore, Slovakia, Slovenia, South Africa, Spain, Taiwan, United Kingdom, United States

Contacts

• Name: Christopher Bruno
• Affiliation: Cubist Pharmaceuticals LLC, an indirect wholly-owned subsidiary of Merck Sharp & Dohme Corp.

• Name: Christopher Bruno
• Affiliation: Cubist Pharmaceuticals LLC, an indirect wholly-owned subsidiary of Merck Sharp & Dohme Corp.

Key inclusion & exclusion criteria

Inclusion criteria:
1. Provide written informed consent prior to any study-related procedure not part of normal medical care. If the subject is unable to do so, local country laws and institution specific guidelines and requirements in place for obtaining informed consent should be met. A legally acceptable representative may provide consent, provided this is approved by local country and institution specific guidelines. If a subject comes to consciousness while still in the study and per the Investigator's
judgment the subject is able to read, assess, understand, and make
his/her own decision to participate in the trial, the subject can agree to
continue study participation and the subject may be re-consented, if
required by local country and institution specific guidelines.

2. Be males or females aged 18 years or older. If female, subject must
not be pregnant or nursing, and is either:
• 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
• Of childbearing potential and meets at least 1 of the following:
- Is practicing an effective method of contraception (eg, oral/parenteral
contraceptives plus barrier method), or
- Has a vasectomized partner, or
- Is currently abstinent from sexual intercourse.
Subjects must be willing to practice the chosen contraceptive method or remain abstinent during the conduct of the study and for at least 35 days after last dose of study medication.
Non-vasectomized males are required to practice effective birth control
methods (eg, abstinence, use of condom, or use of other barrier device)
during the treatment period and for at least 35 days after last dose of
study medication.

3. Intubated (via endotracheal tube, including tracheostomy patients)
and on mechanical ventilation at the time of randomization:

For ventilated HABP:
• At least 1 of the following signs and/or symptoms must be present within the 24 hours prior to intubation OR within the 48 hours after intubation in a patient who has been either hospitalized for =48 hours orwho has been discharged from a hospital within the prior 7 days (includes patients institutionalized in skilled nursing or other long-term care facility):
- A new onset of cough (or worsening of baseline cough)
- Dyspnea, tachypnea, or respiratory rate greater than 30 per minute,
particularly if any or all of these signs or symptoms are progressive in
nature
- Hypoxemia defined as an arterial blood gas partial pressure of oxygen
less than 60 mmHg while the subject is breathing room air, OR a pulse
oximetry oxygen saturation less than 90% while the subject is breathing
room air, OR worsening of the ratio of the partial pressure of oxygen to
the fraction of inspired oxygen (PaO2/FiO2 ratio).

For VABP, receiving mechanical ventilation =48 hours:

Exclusion criteria:
1. Any of the following diagnoses or conditions that interfere with the
assessment or interpretation of outcome:
• Atypical, viral, or fungal (including Pneumocystis jiroveci), known or
suspected community-acquired bacterial pneumonia
• Tracheobronchitis (without documented pneumonia), chemical
pneumonitis, or postobstructive pneumonia
• Active primary or metastatic lung cancer
• Pleural effusions (or empyema) requiring therapeutic drainage, lung abscess, or bronchiectasis
• Cystic fibrosis, acute exacerbation of chronic bronchitis, or active
pulmonary tuberculosis
• New York Heart Association (NYHA) Stage IV Congestive Heart Failure
or Cirrhotic Liver Disease
• Full thickness burns (greater than 15% of total body surface area)
• Severe confounding respiratory condition due to penetrating chest
trauma (i.e., chest trauma with paradoxical respiration).
2. Has a documented history of any moderate or severe hypersensitivity
(or allergic) reaction to any ß-lactam antibacterial;
Note: A history of a rash while on a ß-lactam antibiotic does not
automatically exclude a subject (eg, a subject with history of a mild rash
followed by uneventful re exposure may be considered for enrollment).
3. Received systemic or inhaled antibiotic therapy effective against Gram-negative pathogens that cause VNP, for >24 hours (i.e., >1 dose of a once daily antibiotic, >2 doses of a twice daily antibiotic, etc.) in the 72 hours prior to the first dose of study drug. Drugs with only Gram-positive activity [eg, daptomycin, vancomycin, linezolid] are allowed.
Exceptions:
• Persistent/worsening signs and/or symptoms of VNP are still present despite =48 hours of antibiotic therapy for the treatment of the current VNP, and (a) a LRT culture obtained while the subject is on the failing antibiotic therapy for this episode of VNP showed growth of a Gram-negative pathogen and (b) the isolated pathogen is not known to be resistant to one of the study drugs
• Signs and/or symptoms of VNP develop after receiving =48 hours of prior antibacterial therapy for an indication other than the current VNP
• Treatment with a non-absorbed antibiotic used for gut
decontamination (eg, low-dose erythromycin) or to eradicate C.
difficile.
4. Baseline Gram stain shows the presence of only Gram-positive bacteria.
Exception: If the subject has a lower respiratory tract culture growing a Gram-negative pathogen obtained within 72 hours prior to the first dose of study drug, these results will supersede baseline Gram stain results of only Gram-positive bacteria.
5. Active immunosuppression, including human immunodeficiency virus (HIV) with a known CD4 count of <200 cells/mm3, active hematological malignancy, recipients of solid organ or bone marrow transplants, subjects currently on immunosuppressive therapy including cancer chemotherapy, medications for prevention of transplant rejection, or chronic administration of corticosteroids (defined as >40 mg of prednisone per day administered continu

Age minimum:
Age maximum:
Gender:
Female: yes
Male: yes

Health Condition(s) or Problem(s) studied

Ventilated Nosocomial Pneumonia
MedDRA version: 20.0 Level: LLT Classification code 10052596 Term: Nosocomial pneumonia System Organ Class: 100000015664

Therapeutic area: Diseases [C] - Bacterial Infections and Mycoses [C01]

Intervention(s)

Trade Name: Zerbaxa
Product Name: Ceftolozane/Tazobactam
Product Code: CXA-201
Pharmaceutical Form: Powder for solution for infusion
INN or Proposed INN: Not yet available
CAS Number: 936111-69-2
Current Sponsor code: CXA-101
Other descriptive name: CEFTOLOZANE SULFATE
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 1000-
INN or Proposed INN: Tazobactam Sodium
CAS Number: 89785-84-2
Other descriptive name: TAZOBACTAM SODIUM
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 500-

Trade Name: Meronem
Product Name: Meropenem
Pharmaceutical Form: Powder for solution for injection/infusion
INN or Proposed INN: pending
Current Sponsor code: CXA-NP-11-04
Other descriptive name: MEROPENEM TRIHYDRATE
Concentration unit: g gram(s)
Concentration type: equal
Concentration number: 1-

Primary Outcome(s)

Secondary Objective: • To compare the clinical response rates of ceftolozane/tazobactam
versus meropenem in adult subjects with VNP at the TOC visit (7 to 14
days after the EOT visit) in the ITT population.

• To compare the clinical response rates at the TOC visit (ceftolozane/tazobactam versus meropenem) in the subset of subjects who had P. aeruginosa isolated from the baseline LRT culture.

Timepoint(s) of evaluation of this end point: Test of Cure (TOC) visit

Main Objective: To demonstrate the non-inferiority of ceftolozane/tazobactam versus
meropenem in adult subjects with VNP based on the difference in clinical response rates in the Clinically Evaluable (CE) population at the TOC visit (7 to 14 days after the EOT visit), using a non-inferiority margin of 12.5%.

Primary end point(s): Clinical response at the TOC visit in the CE population.

Secondary Outcome(s)

Secondary end point(s): Key Secondary Endpoints:
• Clinical response at the TOC visit in the ITT population.
• Clinical response at the TOC visit in the mITT population
• Clinical response for subjects at the TOC visit in the subset of subjects
who had P. aeruginosa isolated from the baseline LRT culture in the
mITT population.

Other Secondary Endpoints:
• Clinical response for subjects at the TOC visit in the subset of subjects
who had Enterobacteriaceae isolated from the baseline LRT culture in
the mITT population
• Per-subject microbiological response at TOC in the ME population
• Per-pathogen microbiological response for P. aeruginosa at TOC in the
ME population
• Per-pathogen microbiological response for Enterobacteriaceae at TOC in the ME population
• Per-pathogen microbiological response at TOC in the ME population
• Day 28 all-cause mortality in the ITT population
• Day 14 all-cause mortality in the ITT population
• Clinical response at EOT in the ITT and CE populations
• Clinical response at the LFU visit in the CE population
• Per-subject microbiological response at EOT in ME population
• Per-pathogen microbiological response at EOT in the ME population
• Per-pathogen clinical response at TOC by baseline MIC in the mITT and ME populations
• Per-pathogen clinical response at TOC by baseline Kirby-Bauer zone
diameter in the mITT and ME populations
• Pharmacokinetics.

Timepoint(s) of evaluation of this end point: Test of Cure (TOC) visit

Secondary ID(s)

2012-002862-11-GB

CXA-NP-11-04

Source(s) of Monetary Support

Cubist Pharmaceuticals LLC, an indirect wholly-owned subsidiary of Merck Sharp & Dohme Corp.

Ethics review

Status: Approved
Approval date:
Contact:

Results

• Results available: Yes
• Date Posted: 30/05/2019
• Date Completed: 06/06/2018
• URL: https://www.clinicaltrialsregister.eu/ctr-search/trial/2012-002862-11/results