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 @ 4:12 AM
Ignite Modification Date:
2025-12-25 @ 4:12 AM
NCT ID:
NCT04385420
Eligibility Criteria:
Inclusion Criteria:
1. Male or female, between 18 and 55 years old, extremes included;
2. Weighed at least 50 kg and had a body mass index (BMI) within normal range: 18.0≤ BMI \<31.0 kg/m2;
3. In good physical and mental health as determined on the basis of medical history and general physical examination performed at screening;
4. Haematology and chemistry parameters, pulse rate and/or blood pressure, and ECG within the reference range for the population studied, or showing no clinically relevant deviations, as judged by the Investigator;
5. Negative urine test for selected drugs of abuse at screening and upon check-in at the clinical site; Note: Subjects could not consume poppy-seeds within 24h before screening and before each urine drug screening because this could falsify the results of the opiate urine drug test.
6. Negative alcohol breath test at screening and upon check-in at the clinical site;
7. Negative hepatitis panel (including hepatitis B surface antigen \[HBsAg\] and anti hepatitis C virus \[HCV\] antibodies) and negative human immunodeficiency virus (HIV) antibody screens;
8. Female subjects had to be of non-childbearing potential, as follows:
1. At least 1 year post-menopausal (amenorrhea \>12 months in the absence of an alternative medical cause and follicle-stimulating hormone \>30 mIU/mL in women not using hormonal contraception or hormonal replacement therapy) prior to screening;
2. Surgically sterile (bilateral oophorectomy, hysterectomy, bilateral salpingectomy, or bilateral tubal ligation);
9. To protect partners from possible exposure to study medication in semen, male subjects had to use a condom during the study, even if they had a vasectomy or their partner was not of childbearing potential.
Note: medically acceptable methods of contraception that could be used by the partner included combined oral contraceptive, contraceptive vaginal ring, contraceptive injection, intrauterine device, and etonogestrel implant;
10. Willing to adhere to the prohibitions and restrictions specified in the protocol (see Appendix 16.1.1);
11. Ability to comprehend the nature of the study and any hazards of participating in it. Ability to communicate satisfactorily with the Investigator and to participate in, and comply with the requirements of, the entire study;
12. Informed Consent Form (ICF) signed voluntarily before any study-related procedure was performed, indicating that the subject understood the purpose of and procedures required for the study and was willing to participate in the study.
Exclusion Criteria:
1. Clinically relevant abnormal history, physical findings, ECG, or laboratory values at the pre-study screening assessment that could interfere with the objectives of the study or the safety of the subject;
2. Presence of acute or chronic illness or history of chronic illness sufficient to invalidate the subject's participation in the study or make it unnecessarily hazardous;
3. A condition that, in the opinion of the Investigator, could compromise the well being of the subject or course of the study, or prevent the subject from meeting or performing any study requirements;
4. Impaired endocrine, thyroid, hepatic, respiratory or renal function, diabetes mellitus, coronary heart disease, cancer, or history of any psychotic mental illness;
5. Respiratory tract infection within 4 weeks before the screening visit;
6. History of surgery or medical intervention, or planned surgery or medical intervention, that could interfere with the objectives of the study or the safety of the subject;
7. Presence or history of severe adverse reaction to any drug, or sensitivity to components of the study medication;
8. Use of a prescription or over-the-counter medicine, with the exception of acetaminophen (paracetamol), during the 7 days (or 5 half-lives, whichever is longer) before the first dose of study medication;
9. Participation in another clinical study of a new chemical entity, new device, or a prescription medicine within the 3 months before dosing, or participation within 5 half-lives of receiving an experimental drug (whichever is longer);
10. Presence or history of drug or alcohol abuse, or intake of more than 21 units (14 units for women) of alcohol weekly;
11. Use of a prohibited therapy;
12. Current smoker; or ex-smokers who (a) gave up less than 1 year ago, or (b) who had a history of more than 10 pack-years; Pack-years = cigarettes per day x number of years smoked/20
13. Blood pressure and heart rate at the screening examination outside the ranges 90 150 mmHg systolic, 40-90 mmHg diastolic; heart rate 40-100 bpm;
14. Loss of more than 400 mL blood, e.g. as a blood donor, or donation of blood products, during the 3 months before the study;
15. History of tuberculosis infection;
16. Receipt of a living vaccine within the 3 months before dosing;
17. Active or latent parasitic infection, visit to a country with a high prevalence of parasitic infections within 3 months before receiving study medication;
18. Positive faecal blood test at screening;
19. Employee of the Investigator or the Sponsor, who was directly involved in the study, or a first-degree relative of such person;
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
55 Years
Study:
NCT04385420
Study Brief:
Protocol Section:
NCT04385420