Expired Study
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Baltimore, Maryland 21225


Purpose:

The purpose of this study is to determine the safety and tolerability of CoFactor in healthy subjects.


Criteria:

Inclusion Criteria: - Males and Females age 18-65 inclusive at screening. - Subject has to agree to practice abstinence or medically accepted contraception and not to participate in sperm donation or in vitro fertilization. - Body Mass Index in the range of 18 to 30 kg/m2 and body weight of 45 to 95 kg. - Subject must be healthy as determined by the investigator on the basis of screening evaluations. - Subject must be nonsmoker or smoker of fewer than 10 cigarettes per day as determined by history. Must be able to abstain from smoking during the in-clinic stay. Exclusion Criteria: - Presence of clinically significant illness within 21 days prior to dosing, viral or bacterial infection, or documented drug allergies that may affect subject's safety during the study. - Laboratory or clinical evidence suggestive of disease. - Clinically significant or predisposing disorder that may interfere with the absorption, distribution, metabolism and/or excretion of drugs. - History of drug abuse within 1 year of dosing and/or admitted alcohol abuse or history of alcohol use that may interfere with the ability to comply. - Pregnant, lactating, or positive pregnancy test. - Clinically significant electrocardiogram abnormalities. - History of positive test for hepatitis B or C, or HIV. - Positive findings of urine narcotic screen. - History of drug allergy.


NCT ID:

NCT00663481


Primary Contact:

Principal Investigator
Ronald Goldwater, MD
Parexel International - Baltimore CPRU


Backup Contact:

N/A


Location Contact:

Baltimore, Maryland 21225
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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