Status:
COMPLETED
Safety of a Hypolipidemic Agent in Healthy Normal Volunteers
Lead Sponsor:
Pharmena North America
Conditions:
Hyperlipidemia
Eligibility:
All Genders
18-50 years
Phase:
PHASE1
Brief Summary
The Purpose of this study is to determine the safety and tolerability of 1-MNA, a drug that is intended to be used in the treatment of elevated levels of blood fats. This study will determine the way ...
Detailed Description
Dyslipidemia is a major risk factor for coronary artery disease (CAD) and its management is important in preventing the occurrence of cardiovascular events. Dyslipidemia occurs when there is an imbala...
Eligibility Criteria
Inclusion
- Good health (based on medical history, physical examination, electrocardiogram, and clinical laboratory tests)
- Non-smokers (refrained from any tobacco usage, including smokeless tobacco, nicotine patches, etc., for 6 months prior to the Screening visit)
- Between 18 and 50 years old (inclusive)
- Body weight within 20% of the desirable weight for adults at the Screening visit
- Able to execute informed written consent (informed consent must be obtained for all subjects before enrollment in the study.
- Willingness to abstain from alcohol and xanthine-containing food and beverages for the duration of each treatment period
- Willingness to remain in the clinic for the inpatient portions of the study
- Female subjects must be non-pregnant and either surgically sterile, postmenopausal for a least 1 year, or using an acceptable method of contraception defined as an oral, implanted, or transdermal contraceptive plus one of the following barrier methods: diaphragm with spermicidal cream/jelly or use of a condom by sexual partner.
Exclusion
- Currently abusing drugs or alcohol or with a history of drug or alcohol abuse within the past two years
- Unwilling or unable to comply with the protocol or reside in the study unit during the study period or to cooperate fully with the principal investigator and site personnel
- Has used any 1) prescription medication within 14 days prior to treatment in either treatment period or 2), or any over-the-counter (OTC) medication, herbal preparations, and/or vitamins within 48 hours prior to the start of study MNA administration on either treatment period of this study.
- Has a clinically abnormal ECG
- Has a serum potassium, sodium, calcium, or magnesium level that is not within normal limits or has other vital signs or clinical laboratory values at the screening visit that are deemed by the principal investigator to make the subject an inappropriate candidate for the study
- Has taken any other investigational drug during the 30 days prior to screening visit
- Has donated or lost more than a unit of blood within 30 days prior to screening visit
- History of renal, hepatic, gastrointestinal, cardiovascular, or hematologic disease
- Serious mental or physical illness within the past year
- Has any condition(s) that in the investigator's opinion would: a) warrant exclusion from the study or b) prevent the subject from completing the study
- Have a positive test for hepatitis B surface antigen, hepatitis C antibody, or HIV antibody at screening
- Be a female subject with a positive serum pregnancy test or who is breast-feeding at screening
- Be unable to understand verbal and/or written English or any other language in which a certified translation of the informed consent is available
- Has a history of hypersensitivity or allergic reaction to Niacin or Nicotinamide
- Has had prior exposure to MNA
- Has a Mental capacity that is limited to the extent that the subject cannot provide legal consent or understand information regarding the side effects or tolerance of the study drug.
Key Trial Info
Start Date :
December 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2008
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00685737
Start Date
December 1 2007
End Date
June 1 2008
Last Update
June 27 2008
Active Locations (1)
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1
Buffalo Clinical Research Center
Buffalo, New York, United States, 14202