Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Caucasian
Signed the written informed consent form before first screening procedure
Age ≥ 18 years and ≤ 55 years
In general good health in the opinion of the investigator
BMI between 20.0 and 28.0 kg/m2
Use of adequate and stable contraception for 3 months prior to study initiation, during the course of the study and 30 days thereafter. Sexually active males must use a condom. Sexually active females must use double-barrier contraception or hormonal contraceptive (oral, transdermal, vaginal ring, implants), or must have undergone clinically documented total hysterectomy and/or oophorectomy, surgical sterilization or be postmenopausal defined by amenorrhea for at least 12 months and confirmed with a FSH higher than 40 IU/mL.
If subjects claim abstinence as their method of contraception, they must be willing to agree to use condoms if they become sexually active from 14 days prior to the first dose of the study drug through 90 days beyond the conclusion of the study.

Exclusion Criteria:

Pregnant women, women planning to become pregnant and breastfeeding women
Subjects with a history of MS in first grade family members
A history of or currently active clinically significant cardiac (including clinically significant ECG abnormalities in the opinion of the PI), pulmonary, gastrointestinal, hepatic, renal, pancreatic, or neurological disease
ALT, AST and/or gamma-GT above 3 times the upper limit of normal
Serum creatinine above 1.5 times the upper limit of normal
Amylase above 1.5 times the upper limit of normal
Hemoglobin < 7.0 mmol/L for females and < 8 mmol/L for males; leucocytes > 20*109/L or < 3.5*109/L; platelets < 125*109/L
SBP > 160 mmHg and/or DBP > 100 mmHg
Known or suspected hypersensitivity to any component of DC-TAB
Known or suspected impairment of the immune system
Acute respiratory or other active infections or illnesses
Fever (oral temperature > 38.0 °C on day 1)
Blood donation or significant blood loss within 90 days of first study medication dosing.
Plasma donation within 7 days of first study medication dosing
Recipients of blood or blood products in the last 6 months
Participation in another clinical study within 90 days of the start of this trial or planning participation in another clinical trial during this study or in the 4 weeks after last visit
Taking immunosuppressive agents, corticosteroids, anti-allergic, anti-coagulation or anti-platelet medication
History of drug addiction (positive drug screen) or excessive use of alcohol (weekly intake more than 28 units of alcohol), or psychological or other emotional problems that are likely to invalidate informed consent, or limit the ability of the subject to comply with the protocol requirements
Positive HIV1, or HIV2 serology
Positive results from the hepatitis serology which indicates acute or chronic hepatitis B or hepatitis C
Positive alcohol breath test
Vaccination with any vaccine within 4 weeks prior to dosing of the study medication
Any physical condition that would, in the opinion of the investigator, place the subject at an unacceptable health risk or risk of injury or render the subject unable to meet the requirements of the protocol
History of serious adverse reactions or hypersensitivity to any medicinal product
Smoking > 5 cigarettes/day or unable to refrain from smoking while confined to the CPU
Use of prescription, over-the-counter (OTC), herbal supplements (excluding hormonal contraceptives, one-a-day vitamins, acetaminophen) within 14 days prior to the first dose of study drug).