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 @ 7:07 PM
Ignite Modification Date:
2025-12-24 @ 7:07 PM
NCT ID:
NCT01000857
Eligibility Criteria:
Inclusion Criteria:
* Healthy Japanese adult males between 20 and 64 years of age inclusive
* BMI 18.50 or higher and \< 25.00 kg/m2, and bodyweight 50 kg or higher
* Non-smokers
* AST, ALT, ALP, gamma-GTP and total-bilirubin are below the upper limit of normal range
* QTc(B) interval \<450 msec
* Able to attend all visits and complete the study
* Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form
Exclusion Criteria:
* Any clinically relevant abnormality on the screening physical examination, vital signs, 12-lead ECG and/or clinical laboratory tests
* Medical history that is not considered as eligible for inclusion in this study by the investigator
* Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of asymptomatic gallstones)
* History of psychiatric disorder or suicide attempts or behaviours
* History or presence of gastrointestinal, hepatic or renal disease or any other condition known to interfere with the absorption, distribution, metabolism or excretion of drugs
* History of sensitivity to any of the paroxetine formulations, or components thereof
* Positive for urine drug screening
* Participation in another clinical study or post-marketing study in which the subject is or will be exposed to an investigational or a non-investigational product or device
* Participation in a clinical study or post-marketing study with an investigational or a non-investigational product or device within 4 months of preceding the first dose of study medication
* History of drug or other allergy, or idiosyncrasy, excluding a pollen allergy without current symptoms
* History of drug abuse, or current conditions of drug abuse or alcoholism
* History of regular alcohol consumption exceeding, on average, 14 drinks/week (1 drink = 150 mL of wine or 350 mL of beer or 45 mL of 80 proof distilled spirits) within 6 months of screening
* Use of prescription or no-prescription drugs, including vitamins, crude drug, herbal and dietary supplements (including St John's Wort) within 14 days prior to the first dose of study medication
* Unwillingness or inability to follow the procedures outlined in the protocol
* Consumption of grapefruit or grapefruit-containing products from 7 days prior to the first dose of study medication
* Positive for syphilis, HIV antibody and antigen, Hepatitis B surface antigen, Hepatitis C antibody or HTLV-1 antibody
* Donation of blood in excess of 400mL within the previous 4 months or 200mL within the previous 1 month to the first dose of study medication
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
20 Years
Maximum Age:
64 Years
Study:
NCT01000857
Study Brief:
Protocol Section:
NCT01000857