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 @ 3:48 AM
Ignite Modification Date:
2025-12-25 @ 3:48 AM
NCT ID:
NCT00668902
Eligibility Criteria:
Inclusion Criteria:
1. Asian male or female subjects between 18 and 49 years of age, who are in good physical health with no significant medical problems or laboratory test abnormalities. Subjects should have normal liver and kidney function.
2. Subjects with BMI \<30 which will be determined by Metropolitan height and weight tables. Subjects must weigh at least 110 pounds.
3. Subjects must agree to refrain from taking any prescription and over-the-counter medications, as well as any herbal medications one week before the start of the study and during the study period.
4. Subjects must agree to refrain from consuming alcohol 48 hours before the start of the study and during the study period.
5. Subjects must be capable of satisfying protocol requirements and be able to sign written informed consent.
Exclusion Criteria:
1. Subjects who have a history of intolerance or allergy to the study drug: pantoprazole.
2. Subjects who have donated blood within the last 60 days of the screening visit or plan to donate blood during the course of the study or within 60 days after study completion.
3. Subjects who have had treatment with any investigational drug within the past 30 days.
4. Subjects who have used illegal drugs within three months prior to enrollment.
5. Female subjects currently taking oral contraceptive birth control pills and who are unwilling or unable to stop oral contraceptives and use a barrier contraceptive method (such as condom, contraceptive foams, etc.) starting from the time of screening phase to the completion of the study.
6. Female subjects who are pregnant or lactating.
7. Subjects who are unreliable in the opinion of the study physician.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
49 Years
Study:
NCT00668902
Study Brief:
Protocol Section:
NCT00668902