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 @ 7:49 PM
Ignite Modification Date:
2025-12-24 @ 7:49 PM
NCT ID:
NCT01374503
Eligibility Criteria:
Inclusion Criteria:
* Healthy male volunteers, aged \>= 18 and \<= 55 at screening.
* Willing to consent to using an effective contraceptive method for at least 3 months after test substance administration.
* Non-smokers, or ex-smokers abstinent from tobacco for at least 1 year.
* Body mass index (BMI): 19 - 29 kg/m2 (extremes included).
* Haematology and chemistry parameters within normal range or showing no clinically relevant deviations, as judged by the Medical Investigator. For haematology, haemoglobin and white blood cell (WBC) count must be within normal limits. For chemistry, calcium, alkaline phosphatase (ALP), (alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transferase (GGT) and lactate dehydrogenase (LDH) must be within normal limits.
* Normal electrocardiogram, showing no clinically relevant deviations, as judged by the Investigator. QTc \<= 450 ms.
* No history or presence of diseases of the kidneys, heart, lungs, liver, gastrointestinal tract or endocrine organs, or other conditions known to interfere with the absorption, distribution, metabolism or excretion of drugs.
* No history of clinically relevant allergies.
* Obtained, signed and dated informed consent.
* Ability and willingness to comply with protocol requirements.
Exclusion Criteria:
* Intake of any prescribed systemic or topical medication within 14 days prior to dosing.
* Intake of vitamin A derivates or retinoids within 30 days prior to the start of drug administration.
* History of thrombosis.
* Chronic infection or acute significant infection or fever within the last 5 weeks prior to the start of test substance administration.
* Subjects with any abnormality of the spleen (confirmed by echography) or history of splenic disease, or subjects that underwent splenectomy in the past.
* Blood donation (\>500 ml) or a comparable blood loss within three months prior to the start of drug administration.
* Subjects who, in the investigator's opinion, may not be capable of following the study schedule for any reason, with special emphasis on eligibility for the aphaeresis procedure.
* Participation in an investigational drug study within 60 days prior to drug administration, or within less than 6 times the terminal elimination half-life of the test substance used in the respective trial (whichever is longer).
* Malignancy, or prior malignancy, with a disease-free interval of \< 5 years after diagnosis and intervention, except curative treatment for non-melanoma skin cancer or resected carcinoma in situ.
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
55 Years
Study:
NCT01374503
Study Brief:
Protocol Section:
NCT01374503