Safety and Efficacy Study of Oral Zabofloxacin in Community Acquired Pneumonia

Stopped early · Phase 2

Conditions studied: Community Acquired Pneumonia

In brief

A double-blind, three-arm study, to evaluate the safety and efficacy of two dosing regimens of zabofloxacin (a fluoroquinolone antibiotic) in community acquired pneumonia.

Key facts

Study ID

NCT01081964

Run by

IASO Pharma Inc.

People needed

48

Starts

2010-03-01

Expected to finish

2012-06-01

Last updated by the study team

2012-05-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female >/= 18 years old
• Documented fever (oral >100°F (37.8°C), tympanic >101°F (38.1°C)must be documented within the time frame of 24 hours prior to first dose through 24 hours after first dose of study drug
• Community-acquired pneumonia of moderate severity (defined as PSI Risk Class II or III) requiring administration of antibiotics
• Dyspnea and/or tachypnea (>20 breaths/minute)
• Clinical diagnosis of pneumonia, as demonstrated by all of the following signs and symptoms:
• new or increased cough
• production of purulent sputum or a change in the character of sputum in subjects who normally have purulent sputum
• auscultatory findings on pulmonary examination of rales and/or evidence of pulmonary consolidation (e.g., bronchial breath sounds, egophony, or dullness on percussion)
• Females must be surgically sterile (e.g., tubal ligation, hysterectomy), post-menopausal at least 2 years, or if of childbearing potential, they must have a negative urine pregnancy test (β-human chorionic gonadotropin [β-hCG]) prior to randomization into the study. Males and females must agree that if they have intercourse that they will use at least two medically accepted methods of birth control (e.g., hormonal contraceptive, intrauterine device, spermicide, or condom) from study entry through 60 days after discontinuation of study drug treatment
• Able to give written informed consent in a manner approved by the Institutional Review Board or Ethics Committee and comply with the requirements of the study

You may not qualify if…

• Subjects must NOT meet any of the following exclusion criteria:
• Received one or more doses of any systemic antibiotic in the last 2 weeks
• Diagnosed with any other infection requiring systemic antibacterial therapy
• Require long-term (>7 days) antibiotic therapy
• Previous diagnosed condition that might mimic or complicate the course and evaluation of the infectious disease process (e.g., septic shock, bronchiectasis, lung abcess or empyema, aspiration pneumonia, active tuberculosis, pulmonary malignancy, cystic fibrosis, post-obstructive pneumonia, etc.)
• Hypothermia (oral <96°F [35.6°C}, tympanic <97°F [35.9°C]
• Hospitalization (inpatient) in the previous 60 days or infection presumably acquired in the hospital
• Resident of a skilled nursing facility anytime in the previous 60 days or infection presumably acquired in a skilled nursing facility
• Chronic infection with Hepatitis B
• Any evidence of, or is a known carrier of , Hepatitis C antibody
• Infection with Clostridium difficile
• Immunocompromising illness, including known human immunodeficiency virus (HIV) positivity or AIDS, organ (bone marrow) transplant recipients, and hematological malignancy
• Psychotic disease, peripheral neuropathy, and glucose-6-phosphate dehydrogenase deficiency; uncontrolled or poorly controlled diabetes. Diabetic subjects who are stable and on a stable course of antihyperglycemic agents for the past 3 months will be permitted in the trial.
• High exposure to sunlight or ultraviolet radiation
• Immunosuppressive therapy, including cancer chemotherapy or chronic use of corticosteroids (i.e., >20mg prednisone or equivalent per day for >/= 14 days within the last 6 months
• History of renal or hepatic disease as defined by at least one of the following:
• Calculated creatinine clearance <50 mL/min (any subject on dialysis must be excluded)
• BUN >/= 30 mg/dL
• ALT or AST > 3x ULN
• Total bilirubin > 2x ULN
• Alkaline phosphatase > 1.25x ULN
• History of or current malabsorption conditions (i.e., short bowel syndrome, active Crohn's disease, celiac disease, etc.)
• Neutropenia as defined by absolute neutrophil count <1000 cells/mm3. Subjects with neutrophil counts as low as 500 cells/mm3 are permitted if the reduction can be documented to be due to the acute infectious process
• Platelet count <75,000/mm3. Subjects with platelet counts as low as 50,000/mm3 are permitted if the reduction is historically stable
• Coagulation tests >1.5x ULN (PT, PTT, or INR). Subjects on anticoagulants with values > 1.5x ULN can be enrolled, provided these values are historically stable and within the therapeutic range

Where it is running

• Study site — Huntsville, Alabama, United States
• Study site — Toney, Alabama, United States
• Study site — Fort Myers, Florida, United States
• Study site — Eagle, Idaho, United States
• Study site — Evansville, Indiana, United States
• Study site — Keego Harbor, Michigan, United States
• Study site — Belvidere, New Jersey, United States
• Study site — Columbus, Ohio, United States
• Study site — Dayton, Ohio, United States
• Study site — Springfield, Ohio, United States
• Study site — Gresham, Oregon, United States
• Study site — Warminster, Pennsylvania, United States
• Study site — Tyler, Texas, United States

Full record on ClinicalTrials.gov

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