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

NCT ID: NCT01905410

Last Updated: 2019-03-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 66 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-07-31
• Study Completion Date: 2014-04-30

Brief Summary

VVZ-149 is a novel analgesic drug candidate that shows a potential analgesic activity inhibiting GlyT2 and 5HT2A simultaneously. There have been many efforts to develop single-target selective drugs to treat pain, but usually unsuccessful due to the lack of efficacy or limitations of single-target approach for new drug discovery. VVZ-149 is expected to have a dual-target activity, demonstrated having a synergism between GlyT2 and 5HT2A antagonistic activities to maximize an antinociceptive effect in the in vivo animal models. Now the investigators are developing VVZ-149 as an IV injection to treat post-operative pain.

The primary objective of this study is to evaluate a safety, tolerability and pharmacokinetic properties of VVZ-149 injection with placebo in healthy male volunteers. This Phase 1 study consists of a randomized, double-blind, placebo controlled, single and multiple ascending dose (SAD & MAD) escalation clinical trials.

Detailed Description

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

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

single treatment - VVZ-149 Injection

single ascending dose escalation

• 0.25, 0.5, 1, 2, 4, 6, and 8 mg/kg Cohorts
• 4 hours IV infusion

Group Type: EXPERIMENTAL

VVZ-149 Injection

Intervention Type: DRUG

VVZ-149 in water for injection

single treatment - placebo

• The matching volume of placebo (water for injection) to each experimental cohort
• 4 hours IV infusion

Group Type: PLACEBO_COMPARATOR

placebo

Intervention Type: DRUG

water for injection

multiple treatment - VVZ-149 Injection

Based on the results of SAD trials, low and high dosage are determined for MAD trials.

• high and low dosage
• 4 hours IV infusion x 2 times/day x 3 days

Group Type: EXPERIMENTAL

VVZ-149 Injection

Intervention Type: DRUG

VVZ-149 in water for injection

multiple treatment - placebo

• The matching volume of placebo (water for injection) to each experimental cohort
• 4 hours IV infusion x 2 times/day x 3 days

Group Type: PLACEBO_COMPARATOR

placebo

Intervention Type: DRUG

water for injection

Interventions

VVZ-149 Injection

VVZ-149 in water for injection

Intervention Type: DRUG

placebo

water for injection

Intervention Type: DRUG

Other Intervention Names

VVZ-149 Injection or Water for injection; VVZ-149 Injection or Water for injection

Eligibility Criteria

Inclusion Criteria

1. willingness to sign the written informed consent form (ICF)

2. 20~45 years, inclusive, healthy male

3. 50~90kg, inclusive, and within the 20% of ideal body weight

4. compatible at screening ( medical history, physical examination, vital signs, ECG, haematology, clinical chemistry, urinalysis)

5. 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.

Exclusion Criteria

1. 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

2. History of hypersensitivity reactions significant clinically or hypersensitivity reaction to the investigational product, the drugs containing identical ingredient, or other drugs (aspirin, antibiotic etc.)

3. Family history of significant chronic pain disease or case of the immediate family (parent or brother) with chronic pain disease

4. Electrocardiogram QTc > 430 ms, PR interval > 200 msec, QRS interval > 120 msec, or any other clinically significant opinion at screening, exclusive

5. 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

6. Abnormal blood pressure (systolic > 150 mmHg or < 90 mmHg, diastolic > 95 mmHg or < 60 mmHg) in vital signs at screening, exclusive

7. history of drug abuse, positive screen on the an alcohol breath test and an urine drug screening

8. 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)

9. Participation in a drug study (clinical trials) within 2 months prior to drug administration

10. 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

11. 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

12. 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.

13. 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.

14. 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.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Vivozon, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jae Yong Chung, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Bundang Hospital

Locations

Seoul National University Bundang Hospital

Sungnam-Si, Gyeonggi-do, South Korea

Countries

South Korea

Other Identifiers

PT-VVZ149-01

Identifier Type: -

Identifier Source: org_study_id