A Study to Evaluate Safety and Efficacy Following Dosing of Oxycodone/Naltrexone for Treatment of Adults With Pain Following Bunionectomy Surgery

The study is designed to evaluate the safety and efficacy of oxycodone/naltrexone (a) and
oxycodone/naltrexone (b) versus placebo. During the blinded phase of the study (inpatient
portion) the dosing regimen is 1 capsule containing Oxycodone Hydrochloride plus Naltrexone
Hydrochloride (a) or Oxycodone plus Naltrexone Hydrochloride (b) or placebo taken with 4 to
6 ounces (oz) of water every 6 hours (q6h) for 48 hours following the first dose
(Multiple-dose Period) while in-house. Then for the open-label phase of the study
(outpatient portion) dosing will occur every 4 to 6 hours prn with Oxycodone plus
naltrexone. The active and placebo study medications will appear identical. Study subjects
with acute postoperative pain of moderate to severe intensity following unilateral
bunionectomy surgery will be randomized after surgery, and will stay at the study center for
the duration of the 48-hour double-blind period after dose 1 of study medication. The study
will be conducted in the following 4 periods: 1) a pre-treatment period, 2) a multiple-dose
inpatient period (double-blind), 3) a multiple-dose outpatient period (open-label), and 4)
End of Study/Follow-up.

Inclusion Criteria:

1. Complete the informed consent process as documented by a signed informed consent form
(ICF).

2. Be in generally good health and classified as either PS-1 or PS-2 by the American
Society of Anesthetists (ASA) Physical Status Classification System.

3. Be male or female, age 18 to 75 years, inclusively at the time of screening.

4. Be scheduled for a primary, unilateral, distal, first metatarsal bunionectomy with
osteotomy and internal fixation (with no collateral procedures)

5. Female subjects are eligible only if all of the following apply:

- Not pregnant (subjects of child-bearing potential must have a negative serum
beta-human chorionic gonadotropin (B-hCG) pregnancy test at screening and a
negative urine pregnancy test before surgery);

- Not lactating;

- Not planning to become pregnant within the duration of study;

- Surgically sterile (bilateral tubal ligation or hysterectomy), or at least two
years postmenopausal, or is practicing an acceptable form of birth control
(defined as the use of an intrauterine device [IUD], a barrier method with
spermicide, condoms, any form of hormonal contraceptives, partner with a
vasectomy (surgery at least 6 weeks prior to start of surgery) or abstinence )
for at least 3 months prior to the screening visit and agrees to continue
acceptable methods of contraception until one week following the last dose of
ELI-200.

6. Be willing to complete the pain assessments and return to clinic as scheduled.

7. Subjects must experience postoperative pain (Day 1) that is at least moderate as
measured by a NRS score ≥ 4 on a 0-10 NRS, less than 9 hours after discontinuing the
nerve block.

Exclusion Criteria:

1. Have an uncontrolled medical condition, serious intercurrent illness, clinically
significant general health condition, or extenuating circumstance that may
significantly decrease study compliance or otherwise preclude their participation in
the study.

2. Have a clinically significant abnormal electrocardiogram (ECG) at screening as
determined by the Investigator.

3. Have had any type of gastric bypass surgery or have a gastric band. Have previous
abdominal surgery within the past year or history of abdominal adhesions, known or
suspected paralytic ileus.

4. Have a history of any medical condition or surgical procedure that would alter the
absorption, distribution, metabolism or excretion of oxycodone or any opioid
including but not limited to severe chronic diarrhea, chronic constipation, irritable
bowel syndrome, or bowel resection.

5. Have a history of severe bronchial asthma, hypercarbia, or hypoxia (oxygen partial
pressure [PO2] <92%) or any respiratory condition that, in the opinion of the
investigator, makes the subject unsuitable for the study. Mild episodic asthma or
exercised induced asthma will be allowed.

6. Have, in the opinion of the investigator, a clinically significant abnormality on
their clinical laboratory values (urinalysis, hematology and chemistry) at screening.

7. Have glycosylated hemoglobin (2c) > 7%.

8. Have Addison's disease, benign prostatic hyperplasia, or kidney disease or other
conditions as outlined in the Investigator's Brochure or the Percocet and Oxycontin
Package Inserts that are contraindicated for use.

9. Have made a donation (standard donation amount or more) of blood or blood products
(with the exception of plasma as noted below) within 56 days prior to Day -1 .

10. Have made a plasma donation within 7 days prior to Day -1.

11. Have a known allergy or hypersensitivity to any opioid analgesics, naltrexone,
anesthetics (eg, propofol), acetaminophen, NSAIDs (eg, ibuprofen or naproxen,
ketorolac) or any of the excipients

12. Have a known allergy or hypersensitivity to ropivacaine, Mepivacaine, Lidocaine or
any related drug.

13. Have a history of significant intolerance (in the opinion of the investigator) or
allergic hypersensitivity reaction to opioid use.

14. Not be willing to discontinue the prohibited medications, within the allotted time
before surgery and throughout the duration of their participation in the study.

15. Have a history of substance(more than recreational use) or alcohol (more than 14
drinks in a week) abuse within 2 years before screening.

16. Have a positive drug screen or alcohol screen result.

17. Use of anti-coagulant agents (eg, Coumadin, heparin, etc)

18. Have a positive test for human immunodeficiency virus (HIV), hepatitis B virus (HBV),
or hepatitis C virus (HCV) at the screening visit.

19. Have an active malignancy of any type, or has been diagnosed with cancer within 5
years prior to screening (excluding squamous or basal cell carcinoma of the skin).

20. Have dysphagia and/or cannot swallow study medication whole.

21. Use concurrent therapy that could interfere with the evaluation of efficacy or safety
parameters in the opinion of the investigator. (eg, any drugs, in the investigators
opinion, that may exert significant analgesic properties or act synergistically with
oxycodone, morphine, ketorolac, acetaminophen or ibuprofen).

22. Have a history of seizures or history of serious head injury.

23. Must not be a member of a vulnerable population as defined by the Code of Federal
Regulations Title 45, Part 46, Section 46.111(b), including but not limited to
employees (temporary, part-time, full-time, etc.) or a family member of the research
staff conducting the study, or of the Sponsor, or of the Clinical Research
Organization.

24. Have previously participated in a clinical trial using (Oxycodone Hydrochloride
Naltrexone Hydrochloride, 1.5 mg or Oxycodone Hydrochloride , Naltrexone
Hydrochloride 3.0 mg ).

25. Have a history of major mental illness that in the opinion of the Investigator may
affect the ability of the subject to participate in the study. Institutionalized
subjects will not be eligible for participation.

26. Been exposed to any investigational agent within 30 days or five half-lives
(whichever is longer) prior to check-in for Day 1, Period 1, or is scheduled to
receive an investigational device or drug (other than test product) during the course
of this study.

Day -1 Exclusions:

1. Have taken any of the following drugs within the indicated times before surgery:

- over-the-counter or prescription non-steroidal anti-inflammatory drugs (NSAIDs) (such
as ibuprofen [Advil®, Motrin®]), acetaminophen, or naproxen sodium (Anaprox®, Aleve®)
within 24 hours; a daily dose of 81 mg of aspirin will be allowed (higher doses must
be lowered to 81 mg a day by 72 hours prior to surgery).

- naproxen sodium sustained-release (Naprelan®) within 72 hours

- C-2 inhibitors (such as piroxicam or indomethacin) within 5 days

- oxycodone-containing drugs and other analgesic drugs containing opioids within the
past 14 days

- immediate-release sedating antihistamines, tranquilizers, or hypnotics within at
least 6 hours, or long-acting or sustained-released forms of these drugs within at
least 7 days of Day -1

Day 1 Exclusion:

1. Have surgical complications (Day -1) that could compromise the safety of the subject or
confound the results of the trial or any other reason that, in the opinion of the
investigator, makes the subject unsuitable to participate.