Safety of a Hypolipidemic Agent in Healthy Normal Volunteers (PNAI-002)

This study has been completed.
Sponsor:
Information provided by:
Pharmena North America
ClinicalTrials.gov Identifier:
NCT00685737
First received: May 23, 2008
Last updated: June 25, 2008
Last verified: June 2008
  Purpose

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 that 1-MNA is handled by the body, and will also determine its effect on commonly measured blood fat parameters.


Condition Intervention Phase
Hyperlipidemia
Drug: 1-MNA
Drug: Placebo
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Pharmacokinetics/Dynamics Study
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Official Title: A Randomized Placebo Controlled Double Blind Two Period Cross-Over Study to Assess the Safety and Pharmacokinetics and Pharmacodynamics of Oral Dosages of 1-MNA, (A Hypolipidemic Agent) in Healthy Volunteers

Resource links provided by NLM:


Further study details as provided by Pharmena North America:

Primary Outcome Measures:
  • The single dose pharmacokinetics and safety of 1-MNA and an assessment of any gender-based differences in plasma pharmacokinetics [ Time Frame: Over 24 hours following a dose ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • The effect of 1-MNA on triglycerides and lipase activity and lipid profiles after single oral dosages [ Time Frame: Over 24 hours following a single dose ] [ Designated as safety issue: No ]

Enrollment: 20
Study Start Date: December 2007
Study Completion Date: June 2008
Primary Completion Date: June 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
1-MNA-Low Dose
Drug: 1-MNA
Capsule
Other Name: 1-MNA
Active Comparator: 2
1-MNA-High Dose
Drug: 1-MNA
Capsule
Other Name: 1-MNA
Placebo Comparator: 3
Placebo
Drug: Placebo
Capsule
Other Name: Placebo Comparator

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 imbalance in the metabolism and clearance of lipoproteins resulting in lipoprotein overproduction or deficiency. Lipid related risk factors for atherosclerotic coronary artery disease include elevated levels of total cholesterol (TC), triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), intermediate-density lipoprotein cholesterol (IDL-C), very low-density lipoprotein cholesterol (VLDL-C) and reduced concentrations of high-density lipoprotein cholesterol (HDL-C). This lipid risk profile frequently occurs in association with other cardiovascular risk factors (e.g., obesity, elevated blood pressure, diabetes mellitus), and is associated with premature atherosclerosis (NCEP, 2002).

The Main purpose of this study is to formally evaluate the safety and pharmacokinetics and pharmacodynamics of 1-MNA, a hypolipidemic agent with previous human exposure in normal subjects and patients with Hyperlipidemia.

  Eligibility

Ages Eligible for Study:   18 Years to 50 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • 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 Criteria:

  • 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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00685737

Locations
United States, New York
Buffalo Clinical Research Center
Buffalo, New York, United States, 14202
Sponsors and Collaborators
Pharmena North America
Investigators
Principal Investigator: Charles H Ballow, Pharm D. Buffalo Clinical Research Center
  More Information

No publications provided

Responsible Party: Charles Ballow, Pharm D. FACCP, Buffalo Clinical Research Center
ClinicalTrials.gov Identifier: NCT00685737     History of Changes
Other Study ID Numbers: PNAI-002
Study First Received: May 23, 2008
Last Updated: June 25, 2008
Health Authority: United States: Food and Drug Administration

Keywords provided by Pharmena North America:
Hyperlipidemia

Additional relevant MeSH terms:
Hyperlipidemias
Dyslipidemias
Lipid Metabolism Disorders
Metabolic Diseases
Hypolipidemic Agents
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Lipid Regulating Agents
Therapeutic Uses

ClinicalTrials.gov processed this record on September 18, 2014