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 @ 4:23 AM
Ignite Modification Date:
2025-12-25 @ 4:23 AM
NCT ID:
NCT00892320
Eligibility Criteria:
Inclusion Criteria:
* Japanese volunteers must have been born in Japan of Japanese parents and not lived outside of Japan for more than 5 years
* Female volunteers must be surgically sterile, or practicing an effective method of birth control (e.g., prescription oral contraceptives, contraceptive injections, intrauterine device, double-barrier method, contraceptive patch, male partner sterilization) before entry and throughout the study, have a negative serum beta-HCG pregnancy test at screening and a negative urine pregnancy test on Day -1
* Volunteers must sign an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study
* Volunteers must sign informed consent document for pharmacogenomic testing
* However, participation in the genetic testing component is not mandatory for participation in the remainder of the study
* Volunteers must have a weight as defined by Body Mass Index or Quetelet Index (weight \[kg\]/height (m)²) within the range of 18.0 - 25.0, extremes included and must be normotensive with supine (5 min) blood pressure between the range of 100-139 mm Hg systolic and 60-89 mm Hg diastolic
* Volunteers must be healthy on the basis of a pre-study physical examination, medical history, electrocardiogram, and the results of blood biochemistry and hematology tests and a urinalysis carried out less than 3 weeks before the first dose. If the results of the biochemistry or hematology tests or the urinalysis testing are not within the laboratory's reference ranges the volunteer can be included only on condition that the investigator judges that the deviations are not clinically significant. For liver function tests (AST, ALT, bilirubin) the values must be within 2 times the upper limit of the normal reference ranges
* Volunteers must smoke less than 10 cigarettes per day and agree not to change smoking habits during the study
Exclusion Criteria:
* Relevant history of any significant and/or unstable cardiovascular, respiratory, neurologic (including seizures or significant cerebrovascular), renal, hepatic, endocrine, psychiatric, or immunologic disorders
* History of any severe preexisting gastrointestinal narrowing (pathologic or iatrogenic)
* Inability to swallow study medication (volunteers may not chew, divide, dissolve, or crush the study medication)
* History or suspicion of alcohol, barbiturate, amphetamine or narcotic abuse
* Drug allergy to risperidone, paliperidone or any of its excipients
* Use of concomitant medication (including vitamins and herbal supplements), except for paracetamol (acetaminophen) and hormonal contraceptives. All other medication must have been stopped at least 14 days before the first dose in the study
* At screening, 2 and 3 minutes after standing, experience a decrease of greater than or equal to 20 mmHg systolic blood pressure, a decrease of greater than or equal to 10 mmHg diastolic blood pressure, or an increase of greater than or equal to 20 beats per minute in heart rate or with symptoms of lightheadedness, dizziness, or fainting upon standing from the supine position
* Positive serology tests for hepatitis B, C or HIV
* Female volunteers that are pregnant, nursing, or planning to become pregnant
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
45 Years
Study:
NCT00892320
Study Brief:
Protocol Section:
NCT00892320