Safety, Tolerability,Pharmacokinetics and Pharmacodynamics of ODM-106 in Healthy Volunteers (FIMPAM)

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.