Phase I Study to Investigate Safety, Tolerability, and Pharmacokinetics of VVZ-149 Injection

In this clinical study, the investigational drug product will be offered as an injectable form in a transparent glass vial that contains VVZ-149 dissolved by water for injection. When administered, the drug will be diluted by normal saline and will be given by intravenous infusion for 4 hours.

SAD study is planned that maximal 7 cohorts of healthy male subjects are administrated single dose of VVZ-149 injection or placebo. The planned groups for dose escalations were 0.25, 0.5, 1, 2, 4, 6, and 8 mg/kg groups. As a pilot study for safety in this first-in-human study, only 3 subjects received active drug are allocated to first two groups each, without subjects for placebo. For the following groups, 6 subjects for active drug and 2 for placebos are allocated after randomized.

MAD study is planned that 2 cohorts of 10 healthy male subjects each were administered multiple doses of VVZ-149 injection or placebo. The final doses of VVZ-149 injection will be determined later based on the results of SAD study. In each group, 7 subjects for active drug and 3 for placebos are allocated after randomized

Subjects are eligible for the study if they met all the following Inclusion Criteria:

• willingness to sign the written informed consent form (ICF)
• 20~45 years, inclusive, healthy male
• 50~90kg, inclusive, and within the 20% of ideal body weight
• compatible at screening ( medical history, physical examination, vital signs, ECG, haematology, clinical chemistry, urinalysis)
• sterility or keep an ascetic life or male subjects and their female sexual partners had to use a following contraception method during the study period *the medical contraception permissible method: condom, at least partner had to take the oral contraceptive over the 3 months or had to use the injection or insertion contraceptives, intrauterine device.

Subjects are to be excluded from participation if any of the following Exclusion Criteria:

• Presence or history of diseases or abnormalities of liver, kidney, nervous system, respiratory system, endocrine system, or cardiovascular system. Presence or history of hemopathy or psychopathy (mood disorder, obsessive compulsive disorder etc.) Carrier of hepatitis virus in content of the liver disease, exclusive
• History of hypersensitivity reactions significant clinically or hypersensitivity reaction to the investigational product, the drugs containing identical ingredient, or other drugs (aspirin, antibiotic etc.)
• Family history of significant chronic pain disease or case of the immediate family (parent or brother) with chronic pain disease
• Electrocardiogram QTc > 430 ms, PR interval > 200 msec, QRS interval > 120 msec, or any other clinically significant opinion at screening, exclusive
• Any of following results in the Clinical laboratory at screening, exclusive

• Exceed 1.25 times of the upper limit of the normal range of AST,AST
• Exceed 1.5 times of the upper limit of the normal range of BUN, Cr
• Out of normal range in Thyroid function (TSH, T4, FT4, T3) parameters
• Abnormal blood pressure (systolic > 150 mmHg or < 90 mmHg, diastolic > 95 mmHg or < 60 mmHg) in vital signs at screening, exclusive
• history of drug abuse, positive screen on the an alcohol breath test and an urine drug screening
• Taking any ETC or oriental medicine within 2 weeks prior to drug administration, taking any OTC or vitamins within a week prior to drug administration, (but could participate in the study if other conditions are considered appropriate by the medical investigator)
• Participation in a drug study (clinical trials) within 2 months prior to drug administration
• Donation of whole blood within 2 months or blood component within a month or receiving a blood transfusion within a month prior to drug administration
• Intake of more than 21 units per week (one unit of alcohol (10 g of pure alcohol) equals approximately 250 mL of beer, 100 mL of wine or 35 mL of spirits), Unable to stop drinking during the study period
• A smoker (if case of non-smoker to stop smoking within 3 months prior to drug administration, they could participate in this study) and positive screen on urine cotinine test.
• Taking food and drink containing caffeine (coffee, tea, a carbonated drink, a coffee milk, and nutritious tonic etc) from 24 hours prior to hospitalization for clinical trial to discharge from hospital, Unable not to take them.
• judged inappropriate because of medical, psychological, social and geographical conditions difficult to participate in the study or difficult to follow the treatment compliance or follow-up guidelines.