Pharmacokinetics and Metabolism of Hydrocodone Bitartrate Controlled-Release (HC-CR) in Subjects With Hepatic Impairment

Zogenix

Status and phase: Completed; Phase 1

Conditions: Hepatic Impairment

Treatments: Drug: 20 mg HC-ER

Study type: Interventional

Funder types: Industry

Identifiers

NCT02242734

ZX002-1001

Details and patient eligibility

About

Determine the influence of hepatic impairment on the pharmacokinetics and metabolism of Hydrocodone Bitartrate Extended-Release (HC-ER) 20 mg capsules

Full description

Pharmacokinetics and relative bioavailability of hydrocodone and its metabolites under fasted conditions

Enrollment: 30 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. All hepatically-impaired subjects must have meet all of the following inclusion criteria to be enrolled into the study:

2. Male or non-pregnant, non-lactating females. Subjects were aged 18-80 years, inclusive.

3. Subjects must have been a clinical diagnosis of chronic hepatic impairment for duration of at least 6 months classified as mild or moderate as per Child-Pugh classification.

4. Hepatic insufficiency was stable with no acute episodes of illness within the previous 2 months due to deterioration of hepatic function due to any etiology.

5. Female subjects of childbearing potential including those who had a tubal ligation surgery but excluded those who did not have a menstrual period for a minimum of 2 years, had a negative pregnancy test at the Screening and Day -1 visits, and consented to use a medically-acceptable method of contraception throughout the entire study period and for 1 week after the study completed. Medically acceptable methods of contraception included were not limited to abstinence, birth control pills or patches, vaginal rings, diaphragm with vaginal spermicide, Intrauterine Device, and progestin implant or injection (used consistently for 3 months prior to study dosing).

6. Subjects voluntarily provided written informed consent.

7. Subjects, in the Investigator's opinion, were able to complete study procedures

   • All healthy control subjects must have met all hepatic subject inclusion criteria as outlined above with the exception of Inclusion Criteria 3 & 4 above which should be substituted with the following to be enrolled into the study:
   • Must have been matched by age (±10 years) and Body Mass Index (BMI) (± 10% of BMI) with some consideration for race and gender to subjects with hepatic impairment.
   • Were medically healthy with no clinically significant abnormalities in their laboratory profile as deemed by the Investigator.

Exclusion criteria

1. Women who were pregnant or breastfeeding
2. Any clinically significant condition that would, in the opinion of the Investigator, preclude study participation
3. Uncontrolled blood pressure, i.e., subject has a sitting systolic blood pressure 180 mmHg or 90 mmHg, and/or a sitting diastolic blood pressure 120 mmHg or 50 mmHg at Screening.
4. Body Mass Index (BMI) >40 kg/m2.
5. Known allergy or hypersensitivity to hydrocodone, or other opioids.
6. Had taken any investigational drug within 30 days prior to the Day 1 Visit or currently enrolled in another investigational drug study.
7. Had used a monoamine oxidase inhibitor within 14 days prior to Day 1.
8. Been taking opioids during the 30 days prior to Day 1 or needing to take opioids during the study period
9. Positive for human immunodeficiency virus (HIV). Healthy control subjects must not have been hepatitis C virus (HCV) positive, hepatically-impaired subjects could be HCV positive but should not have been receiving treatment.
10. History of any illicit substance abuse in the past 2 years or any history of opioid abuse. Subjects should not have been current abusers of alcohol and must have had a negative serum alcohol level at Screening and Day -1.
11. Positive quantitative urine drug screen for illicit drugs, or non-prescribed controlled substances at Screening.
12. Had made a plasma donation within 7 days prior to Day 1.
13. Had made any significant donation or loss of blood within 56 days prior to Day 1.
14. Had taken CYP2D6 and/or CYP3A4 inhibitors within 7 days prior to Day 1 and/or CYP2D6 and/or CYP3A4 inducers within 21 days prior to Day 1.

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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30 participants in 3 patient groups

Mild Hepatic Impairment

Experimental group

Description:

20 mg HC-ER

Treatment:

Drug: 20 mg HC-ER

Drug: 20 mg HC-ER

Drug: 20 mg HC-ER

Moderate Hepatic Impairment

Experimental group

Description:

20 mg HC-ER

Treatment:

Drug: 20 mg HC-ER

Drug: 20 mg HC-ER

Drug: 20 mg HC-ER

No Hepatic Impairment

Experimental group

Description:

20 mg HC-ER

Treatment:

Drug: 20 mg HC-ER

Drug: 20 mg HC-ER

Drug: 20 mg HC-ER