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:
2025-12-24 @ 6:55 PM
Ignite Modification Date:
2025-12-24 @ 6:55 PM
NCT ID:
NCT00961857
Eligibility Criteria:
Inclusion Criteria:
* Female subjects of reproductive potential test negative for pregnancy and agree to use appropriate contraception
* Subject is in good health and is a non-smoker
* Subject is willing to avoid strenuous physical activity during the study
* Subject agrees to refrain from eating grapefruit or grapefruit products during the study
Exclusion Criteria:
* Subject has a history of neoplastic disease (cancer), stroke, chronic seizures, or major neurological disorder. Subject has a history of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, or genitourinary abnormalities or diseases
* Subject consumes excessive amounts of alcohol or caffeinated beverages
* Subject has donated blood, had surgery or participated in another clinical study within the past 4 weeks
* Subject has a history of significant multiple and/or severe allergies to prescription or non-prescription drugs or food
* Subject has a history of hypersensitivity to metformin, sitagliptin, or sitagliptin/Metformin
* Subject is a regular user or past abuser of any illicit drugs
* Subject is unable to refrain from or anticipates the use of any medication, including prescription and non-prescription drugs or herbal remedies during the study.
* Subject is a nursing mother
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT00961857
Study Brief:
Protocol Section:
NCT00961857