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 @ 5:40 PM
Ignite Modification Date:
2025-12-24 @ 5:40 PM
NCT ID:
NCT02408068
Eligibility Criteria:
Inclusion Criteria:
* Healthy male volunteers between 18 and 60 years of age, inclusive (at screening)
* A body mass index of 21-28 (inclusive).
* No clinically significant abnormal serum biochemistry, haematology and urine examination values
* A negative urinary drugs of abuse screen. A positive alcohol test may be repeated at the discretion of the investigator.
* Negative Human Immunodeficiency Virus (HIV) and Hepatitis b \& C results
* No clinically significant abnormalities in 12-lead Electrocardiogram (ECG)
* No clinically significant deviation outside the normal ranges for blood pressure and pulse measurements
* Subjects (unless anatomically sterile or where abstaining from sexual intercourse is in line with the preferred and usual lifestyle of the subject) and sexual partners must use effective contraception methods during the trial and for 3 months after the last dose, for example:
* Oral contraceptive + condom
* Intra-uterine device + condom
* Diaphragm with spermicide + condom
* Subjects must be available to complete the study
* Subjects must provide written informed consent to participate in the study
Exclusion Criteria:
* A clinically significant history of gastrointestinal disorder likely to influence drug absorption
* Receipt of regular medication (including high dose vitamins, dietary supplements or herbal remedies)
* Evidence of renal, hepatic, central nervous system, respiratory, cardiovascular or metabolic dysfunction Receipt of any vaccination within the previous one month
* Presence of clinically significant infections (systemic fungal and viral infections, acute bacterial infections)
* Current of previous history of tuberculosis
* A clinically significant history of previous allergy/sensitivity to hydrocortisone and/or dexamethasone
* A clinically significant history of family history of psychiatric disorders/illnesses
* A clinically significant history of drug or alcohol abuse
* Inability to communicate well with the investigator (ie language problem, poor mental development or impaired cerebral function)
* Participation in a New Chemical entity clinical study within the previous four months or a marketed drug clinical study within the previous three months
* Subjects who have consumed more than two units of alcohol pre day within seven days prior to the first dose or have consumed any alcohol within the 48hr period prior to the first dose
* Donation of greater than or equal to 450ml blood within the previous three months
* Subjects who smoke or ex-smokers who have smoked within six months prior to first dose
* Subjects who work shifts (ie regularly alternate between days, afternoons and nights)
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
60 Years
Study:
NCT02408068
Study Brief:
Protocol Section:
NCT02408068