Overview

A Randomized, Open Label, Prospective Study to Explore the Clinical Characteristics of Oral MNK155 and Norco 7.5mg/325 When Used for the Treatment of Moderate to Severe Post Operative Pain

Status:
Terminated
Trial end date:
2015-12-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to explore the clinical characteristics oral MNK155 and Norco® 7.5mg/325mg when used for the treatment of moderate to severe post operative pain.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Neil Singla
Collaborator:
Mallinckrodt
Treatments:
Acetaminophen, hydrocodone drug combination
Criteria
Inclusion Criteria:

1. Subjects who provide written informed consent prior to enrollment.

2. Male or female and 18 years of age or older.

3. Subjects who are scheduled to undergo elective general surgery including, but not
limited to the following surgical types:

- Abdominal surgery

- Orthopedic surgery

- Spine surgery

- Genitourinary surgery

4. Subjects classified as American Society of Anesthesiologists (ASA class I-III).

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

- Not pregnant (subjects of child bearing potential must have a negative beta human
chorionic gonadotropin (β-hCG) pregnancy test before surgery);

- Not lactating;

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

6. Subjects who are expected to have acute pain requiring oral opioid analgesics for at
least 48 hours during the post operative period (either inpatient or outpatient).

7. Subjects who are willing and capable of understanding and cooperating with the
requirements of the study.

8. Subjects able to understand and communicate in English.

Exclusion Criteria:

1. Subjects with a medical condition that, in the Investigator's opinion, could adversely
impact the subject's participation, safety, or conduct of the study such as but not limited
to a history of severe renal or hepatic impairment, severe active hepatic disease, or any
other clinically significant medical condition that may preclude safe study participation.