Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 2:00 AM
Ignite Modification Date: 2025-12-25 @ 2:00 AM
NCT ID: NCT00803894
Eligibility Criteria: Inclusion Criteria: * Patient is a male * Patient has no clinically significant abnormality on electrocardiogram performed * Patient agrees to not to consume apple juice, grapefruit or grapefruit products beginning 2 weeks prior to first dose of study drug and for the duration of the study * Patient has been a nonsmoker and/or has not used nicotine or nicotine-containing products for approximately 6 months. * Patient is willing to not use any hair enhancement product or procedures for the duration of the study (for example, permanents, hair straightening techniques) * Patient has a full head of hair * Patient has at least 90% non-gray hair Exclusion Criteria: * Patient has had treatment with any investigational therapy during the prior 21 days * Patient has any history of significant gastrointestinal abnormalities within the last 10 years * Patient has a history of any long-term or active liver disease including elevated liver blood tests. Any patient with a history of Hepatitis B or C (and/or treated previously) will be excluded * Patient has a known history or family history of aortic valve disease, congenital (from birth) heart disease or deafness, hearing loss or early onset Alzheimer's disease (onset at age \< 55) * Patient has a known sensitivity to the ingredients in the drug * Patient has had active and uncontrolled infection within the past month * Patient is HIV positive * Patient has a history of stomach, intestine, heart, blood, liver, brain, kidney, lung, bladder or endocrine abnormalities or diseases * Patient has a history of cancer except for certain skin cancer (basal cell) * Patient has a history of multiple and/or severe allergies or has had an allergic reaction to food or prescription/non-prescription drugs * Patient has had major surgery, donated or lost 1 unit of blood (about 500 mL) within the past month * Patient has premature graying hair (\> 10% gray hair) * Patient has male pattern hair loss * Patient has a prior history of high blood pressure * Patient uses any medication, including prescription and non-prescription drugs or herbal remedies (such as St. John's Wort) beginning approximately 2 weeks prior to the first dose of study drug, throughout the study until the post study visit * Patient consumes excessive amounts of alcohol (greater than 3 glasses of alcoholic beverages) * Patient consumes excessive amounts (greater than 6 servings) of coffee, tea, cola or other caffeinated beverages per day * Patient is a regular use (including "recreational use") of any illicit drugs, has a positive urine drug screen before randomization or has a history of drug (including alcohol) abuse within approximately the past 2 years * Patient has prior exposure to MK 0752 with the past 21 days
Healthy Volunteers: True
Sex: MALE
Minimum Age: 18 Years
Maximum Age: 35 Years
Study: NCT00803894
Study Brief:
Protocol Section: NCT00803894