Overview

Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injection for Postoperative Pain Following Total Hip Arthroplasty.

Status:
Completed
Trial end date:
2018-07-19
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this phase 2 study is to evaluate the efficacy and safety of an analgesic drug candidate, VVZ-149 Injections. The study is designed as randomized, double-blind, parallel, and placebo-controlled study.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Vivozon, Inc.
Treatments:
Analgesics
Criteria
Inclusion Criteria:

1. Patient between the ages of 25 and 65 years old

2. Male patient, in the case of female patient, postmenopausal women, or women physically
incapable of childbearing

3. Subject who underwent surgery specially for the clinical study

4. Ability to provide written informed consent prior to any study procedures.

5. Ability to understand study procedures and communicate clearly with the investigator
and staff.

6. Subjects with body weight under 100kg and body mass index (BMI) level lower than 35
kg/m2, inclusive

7. Single-side surgery patient

Exclusion Criteria:

< Surgical Factors >

1. Emergency or unplanned surgery.

2. Repeat operation

< Subject Characteristics >

3. Women with childbearing potential, Women who are pregnant or breastfeeding.

4. Unstable or poorly controlled psychiatric condition (e.g., untreated PTSD, anxiety, or
depression). Subjects who take stable doses of antidepressants and anti-anxiety drugs
may be included.

5. Unstable or acute medical condition (e.g., unstable angina, congestive heart failure,
renal failure, hepatic failure, AIDS).

6. Subjects who have long QPR (>200msec) or prolonged QTc (> 450msec in male, >470msec in
female) at Screening

< Drug, Alcohol, and Pharmacological Considerations >

7. History of alcohol, opiate or other drug abuse or dependence within 12 months prior to
Screening .

8. Ongoing or recent (within 6 hour prior to surgery) use of steroids, opioids, or
antipsychotics.

9. Alcohol consumption within 24 hours of surgery.

10. Use of nonsteroidal anti-inflammatory drugs (NSAIDs) or acetaminophen within 6 hours
of surgery.

11. Use of herbal agents or nutraceuticals (i.e., chaparral, comfrey, germander, jin bu
huan, kava, pennyroyal, skullcap, St. John's wort, or valerian) within 7 days prior to
surgery.

< Anesthetic and Other Exclusion Considerations >

12. Use of neuraxial or regional anesthesia related to the surgery.

13. Use of ketamine, gabapentin, pregabalin, or lidocaine (>1 mg/kg) intra or
peri-operatively, or within 24 hours of surgery.

14. Subject with known allergies to hydromorphone.

15. Subjects who received another investigational drug within 30 days of scheduled surgery