Status:
COMPLETED
Monoclonal Antibody for Treatment of Inhalation Anthrax
Lead Sponsor:
National Institute of Allergy and Infectious Diseases (NIAID)
Conditions:
Bacillus Anthracis (Anthrax)
Eligibility:
All Genders
18-50 years
Phase:
PHASE1
Brief Summary
The purpose of this study is to evaluate the safety and pharmacokinetics (how long a drug stays in the bloodstream and how high the levels of the drug are at different times) of ETI-204 following intr...
Detailed Description
This initial study with ETI-204 will examine the safety and pharmacokinetics of ETI-204 following IV administration both in the absence and presence of ciprofloxacin. The pharmacokinetics of ciproflox...
Eligibility Criteria
Inclusion
- Healthy male or female subjects between the ages of 18-50 inclusive at the time of enrollment. In each of the drug cohorts (subgroups), at least two of the subjects must be female.
- The following screening laboratory parameters must be within the normal range: AST, ALT, alkaline phosphatase, hemoglobin, and serum creatinine. No repeat testing is allowed for these analytes. For any other clinical chemistry analyte or CBC (including differential and platelet count) parameter that is outside the normal range, the PI and the sponsor's medical monitor will confer and must agree in writing that the value has no clinical significance before the subject will be allowed to enter the study.
- The values for the following tests at screening are to be:
- G-6-P dehydrogenase - normal HBsAG - negative HBV - negative Anti-HCV - negative Anti-HIV (HIV antibody test) - negative Urine drug screen (including cotinine) - negative
- Female subjects of childbearing potential must agree to practice abstinence or to use a licensed, effective form of birth control (e.g., oral contraceptives, diaphragm or condom in combination with contraceptive jelly, cream or foam, intrauterine contraceptive device, Depo-Provera®, skin patch, vaginal ring, or cervical cap) for at least 30 days prior to enrollment and for the duration of the study, including the follow-up period. Females using hormonal contraceptives must agree to use at least one other method for at least 30 days prior to enrollment and for the duration of the study, including the follow-up period.
- Female subjects must have a negative pregnancy test.
- No history of hospitalization for illness within the six months prior to study enrollment.
- Non-smoker or ex-smoker. If a subject is an ex-smoker, he/she must not have used nicotine for at least 6 months prior to enrollment. This will be confirmed by a negative urine test for cotinine.
- Able to spend the two days specified in the study schedule confined in a facility under study rules.
- Able to read, understand and sign the Informed Consent form.
Exclusion
- Routine consumption of any medication (prescription or OTC), vitamin, mineral, antacid, or dietary supplement, for one week before and during the study. The sole exception are hormonal contraceptive agents, as detailed above, hormone replacement therapy, and thyroid replacement therapy. Subjects must be specifically reminded that antacids are excluded.
- Blood pressure greater than 145 mm Hg systolic and 95 mm Hg diastolic.
- Contraindication to the use of ciprofloxacin or any quinolone. (Part 2 only).
- Contraindication to the use of any monoclonal antibody.
- Medical condition that in the Investigator's opinion could adversely impact the subject's participation, safety or conduct of the study.
- Subject has taken an investigational medication in the previous three months.
- The subject has a history of drug or alcohol abuse within the past two years.
- The subject is female and plans to become pregnant during the study or the 42 day follow-up period.
- Calculated Body Mass Index (BMI) greater than 35 or less than 18.5.
- The subject has been previously vaccinated with anthrax or has participated in clinical research involving anthrax.
- Any EKG abnormality except for the following:
- Sinus bradycardia in younger, athletic subjects
- Mild first degree A-V block (P-R interval \< 0.23 sec)
- Mild right or left axis deviation
- Incomplete right bundle branch block DMID does not allow for exceptions of eligibility criteria waivers for enrollment.
Key Trial Info
Start Date :
October 1 2005
Trial Type :
INTERVENTIONAL
End Date :
March 1 2006
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT00138411
Start Date
October 1 2005
End Date
March 1 2006
Last Update
August 27 2010
Active Locations (1)
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1
Ohio State University
Columbus, Ohio, United States, 43210-1239