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 @ 7:56 PM
Ignite Modification Date:
2025-12-24 @ 7:56 PM
NCT ID:
NCT06475404
Eligibility Criteria:
Inclusion Criteria:
* Men aged 18 to 45 years (inclusive) at the time of signing the Informed Consent Form;
* Body mass index (BMI) 18.5 to 29.9 kg/m2, body weight of 50 to 90 kg;
* A verified diagnosis as "healthy" (the diagnosis "healthy" is established based on a detailed medical history, in the absence of deviations from normal values during a clinical examination, including measurement of blood pressure, respiratory rate, heart rate, body temperature, laboratory and instrumental (ECG) examination data);
* A written informed consent to participate in the study in accordance with applicable laws in place and compliance with all the procedures and requirements/restrictions provided for by the study protocol;
* Consent to use adequate methods of contraception (double barrier method-male or female (for partners of male research volunteers), condom with spermicide, intrauterine device (IUD), diaphragm with spermicide, contraceptive sponge, cervical cap with spermicide).
Exclusion Criteria:
* Known hypersensitivity to idursulfase and/or to the medicinal product excipients;
* Burdened allergy history;
* Drug intolerance;
* History of seizures;
* Deposit injections or implants use of any other medicinal product three months before the Screening Visit;
* An unusual way of living (night working, extreme physical activity);
* Diarrhea dehydration, vomiting, or other causes within 24 hours before the Screening Visit;
* Deviations from the normal values of the clinical, laboratory, and ECG examinations;
* If there are acute or chronic diseases of the cardiovascular, bronchopulmonary, nervous, immune, and endocrine systems, diseases of the gastrointestinal tract, liver and biliary tract, kidney and urinary tract, blood and lymphatic system, a history of mental illness;
* Positive results for hepatitis B or C markers, human immunodeficiency virus (HIV), and syphilis;
* Acute infectious diseases less than four weeks before the Screening Visit;
* Regular administration of medicinal products less than two weeks before the Screening Visit;
* Systolic blood pressure (SBP) below 90 mm Hg or above 139 mm Hg; diastolic blood pressure (DBP) below 50 mm Hg or above 89 mm Hg; heart rate (HR) below 60 bpm or above 90 bpm;
* Blood donation (450 mL or more of blood or plasma) less than three months before the Screening Visit;
* Participation in human clinical studies of medicinal products less than three months before the Screening Visit;
* Consumption of more than 5 units of alcohol per week (1 unit of alcohol is equal to 30 ml of ethyl alcohol) OR history of alcoholism, drug addiction, or drug abuse;
* Alcohol exhale positive test;
* Drug addiction and positive urine analysis for potent and narcotic substances;
* Smoking more than 5 cigarettes per day;
* Any planned surgical intervention during the study period;
* Reluctance to comply with contraceptive methods;
* Vaccination (with any vaccine) within 30 days before signing the informed consent and/or the need for vaccination during the study period; 23. History of an autoimmune disease; 24. History of any cancer.
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT06475404
Study Brief:
Protocol Section:
NCT06475404