Arbekacin Treatment of Adult Patients With Infections Caused by Multidrug-resistant Bacteria
NCT ID: NCT01659515
Last Updated: 2020-01-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Brief Summary
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Detailed Description
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Conditions
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Interventions
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Arbekacin Sulfate
Intravenous arbekacin in a total daily dose of 5-7 mg/kg
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Subject is a Walter Reed National Military Medical Center patient deemed by the primary medical or surgical team as having a bacterial infection of the respiratory tract, bloodstream, skin, soft tissue, bone, or genitourinary tract;
3. Subject is allergic to or intolerant of antibiotics to which the infective organism is susceptible; Or The use of antibiotics to which the subject's infective organism is susceptible is contraindicated; Or
Subject's infective organism isolate is a multidrug-resistant (MDR) bacterium defined as any of the following:
* Gram-negative bacterium that is non-susceptible to all index antibiotics within 3 or more of 6 antibiotic classes including aminoglycosides (amikacin, gentamicin, tobramycin), beta-lactam/beta-lactam inhibitor combinations (piperacillin-tazobactam, amoxicillin-clavulanate), carbapenems (imipenem, ertapenem), fluoroquinolones (ciprofloxacin, levofloxacin), cephalosporins (ceftazidime, cefepime, ceftriaxone), and sulbactam (ampicillin-sulbactam);
* Extended Spectrum β-lactamase (ESBL) producing Gram-negative bacterium;
* Carbapenemase resistant Enterobacteriaceae;
* Cephalosporin resistant Klebsiella species;
* Methicillin-resistant Staphylococcus aureus (MRSA);
* Vancomycin resistant Enterococcus species;
* Staphylococcus aureus that is non-susceptible to vancomycin.
4. Subject's infective organism is inhibited in vitro by arbekacin at a concentration ≤ 4 μg/mL;
5. Subject is able to give written or witnessed verbal informed consent \[An exception from the general requirements for informed consent can be made based upon the criteria specified in 21 Code of Federal Regulations 50.23 (a and c)\];
6. Subject has adequate venous access for intravenous administration of arbekacin.
7. Sexually active females, unless surgically sterile or at least 1 year post-menopausal, must have used an effective method of avoiding pregnancy (including oral or implanted contraceptives, IUD, female condom, diaphragm with spermicide, cervical cap, abstinence, use of a condom by the sexual partner, or sterile sexual partner) for at least 30 days prior to receipt of arbekacin and must agree to continue using such precaution for at least 30 days after last dose of arbekacin; the subject must also have a negative pregnancy test within 24 hours prior to initial dose of arbekacin.
Exclusion Criteria
2. Subject is currently participating in another investigational new drug study.
3. Subject has a positive serum pregnancy test or is breast feeding.
18 Years
ALL
No
Sponsors
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Meiji Seika Pharma Co., Ltd.
INDUSTRY
Uniformed Services University of the Health Sciences
FED
U.S. Army Medical Research and Development Command
FED
Responsible Party
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Principal Investigators
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Michael Zapor, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Walter Reed Army Institute of Research (WRAIR)
Locations
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Walter Reed National Military Medical Center (WRNMMC)
Bethesda, Maryland, United States
Countries
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Other Identifiers
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S-11-0001
Identifier Type: -
Identifier Source: org_study_id
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