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 @ 5:18 PM
Ignite Modification Date:
2025-12-24 @ 5:18 PM
NCT ID:
NCT02393950
Eligibility Criteria:
Inclusion Criteria:
* Written informed consent obtained.
* Participants must be able to speak, read and understand German.
* Good general health ascertained by detailed medical history and physical examinations.
* Males 18-45 years (inclusive).
* Body mass index (BMI) 18-30 kg/m2 inclusive
* Weight 55-95 kg (inclusive).
* Participants with female partners of child-bearing potential must adhere to a proper form of contraception from first study treatment administration until 3 months after the end-of-study visit.
Exclusion Criteria:
* A predictable poor compliance or inability to understand and comply with protocol requirements, instructions and protocol-stated restrictions or communicate well with the investigator.
* Vulnerable subjects.
* Veins unsuitable for repeated venipuncture.
* Evidence of clinically relevant cardiovascular, renal, hepatic, haematological, gastro-intestinal, pulmonary, metabolic-endocrine, neurological, urogenital or psychiatric disease as judged by the investigator. The participants should be healthy subjects.
* Subjects with a medical history of relevant psychiatric disorders or evidence of significant neuropsychiatric disease
* Any condition requiring regular concomitant medication including herbal products or likely to need any concomitant medication during the study.
* Definite or suspected personal history of hypersensitivity to drugs or excipients.
* Intake of any medication that could affect the outcome of the study, as judged by the investigator, within 2 weeks before first study treatment administration (2 months for enzyme inducing drugs like rifampicin or carbamazepin), or less than 5 times the half-life of the medication.
* A history of alcoholism or excess alcohol intake (including regular consumption of more than 21 units of alcohol per week) .
* Use of nicotine-containing products within 6 months of admission and inability to refrain from using nicotine-containing products during the study.
* History of drug abuse or positive drug screen for amphetamine, barbiturates, benzodiazepines, cannabinoids, cocaine, opiates, methamphetamine or methadone.
* Propensity to get headache when refraining from caffeine-containing beverages.
* Blood donation or loss of clinically relevant amount of blood within 2 months before the screening visit.
* Abnormal 12-lead ECG finding of clinical relevance at the screening visit
* Heart rate (HR) \< 50 bpm or \> 90 bpm after 10 min in rest (supine) at the screening visit
* At the screening visit: systolic BP \< 90 mmHg or \> 140 mmHg, diastolic BP \< 50 mmHg or \> 90 mmHg, orthostatic hypotension decrease of greater than or equal to 20 mmHg for systolic BP, decrease of greater than or equal to 10 mmHg for diastolic BP.
* Abnormal 24-h Holter of clinical relevance at the screening visit,
* Positive serology to human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg) or hepatitis C virus (HCV) antibodies.
* Any abnormal value of laboratory, vital signs, or physical examination, which may in the opinion of the investigator interfere with the interpretation of the test results or cause a health risk for the subject if he takes part in the study.
* Participation in an investigational drug study within 2 months before entry into this study.
* An employee, a direct or indirect relative of the employee of the contract research organisation or the sponsor.
* Any other condition that in the opinion of the investigator would interfere with the evaluation of the results or constitute a health risk for the subject.
* Subject with abnormal standard EEG judged as clinically relevant by the investigator at screening.
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT02393950
Study Brief:
Protocol Section:
NCT02393950