A Study to Evaluate the Pharmacokinetics of the Hydrocodone Extended-Release Tablet (CEP-33237) in Subjects With Normal Hepatic Function and Subjects With Moderate Hepatic Impairment
Primary Purpose
Hepatic Impairment
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Hydrocodone bitartrate extended-release tablet
Sponsored by

About this trial
This is an interventional treatment trial for Hepatic Impairment focused on measuring Pharmacokinetics, Hydrocodone, Extended Release, Hepatic impairment
Eligibility Criteria
Inclusion Criteria:
All subjects:
- Written informed consent is obtained
Subjects with normal hepatic function:
- The subject is in generally good health (age-appropriate) as determined by medical and psychiatric history, physical examination, ECG, serum chemistry, hematology, coagulation, urinalysis, and serology.
Subjects with hepatic impairment:
- The subject's health is otherwise clinically stable as determined by medical history, physical examination, ECG, serum chemistry, hematology, coagulation parameters (PT, activated partial thromboplastin time [aPTT], and international normalized ratio [INR]), urinalysis, and serology except for those signs and symptoms attributable to liver disease.
- The subject has case record notes demonstrating physical signs consistent with 1 or more of the following characteristic clinical manifestations of liver cirrhosis: liver firmness to palpation, splenic enlargement, spider angiomas, palmar erythema, parotid hypertrophy, testicular atrophy, ascites (accumulation of fluid in the abdominal cavity), or gynecomastia.
- The subject has a Child-Pugh Classification score of 7-9 points (moderate).
Exclusion Criteria:
All subjects:
- The subject has any clinically significant, uncontrolled medical condition.
- The subject is a poor metabolizer of CYP2D6 substrates based on genotyping performed at screening.
- The subject has previously participated in a study with CEP-33237.
- The subject has a known sensitivity or idiosyncratic reaction to hydrocodone or hydromorphone, related compounds, or to any metabolites, or any compound listed as being present in a study formulation.
Subjects with normal hepatic function:
- The subject has a positive test result for HBsAg or antibodies to hepatitis C.
- The subject has a history of alcohol, narcotic, or any other substance abuse.
Subjects with hepatic impairment:
- The subject has severe ascites.
- The subject has an acute exacerbation of liver disease as indicated by worsening clinical signs of hepatic impairment.
Sites / Locations
- Orlando Clinical Research
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Normal Hepatic Function
Moderate Hepatic Impairment
Arm Description
Intervention Drug: Hydrocodone bitartrate extended-release tablet
Intervention Drug: Hydrocodone bitartrate extended-release tablet
Outcomes
Primary Outcome Measures
Pharmacokinetics (AUC and Cmax) after a single dose
Secondary Outcome Measures
Safety (occurrence of adverse events, labs, ECG, physical exam, vital signs, oxygen saturation)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01319279
Brief Title
A Study to Evaluate the Pharmacokinetics of the Hydrocodone Extended-Release Tablet (CEP-33237) in Subjects With Normal Hepatic Function and Subjects With Moderate Hepatic Impairment
Official Title
An Open-Label, Single-Dose, Parallel-Group Study to Assess the Pharmacokinetics of the Hydrocodone Bitartrate Extended-Release Tablet (15 mg) in Subjects With Normal Hepatic Function and Subjects With Moderate Hepatic Impairment
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
August 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cephalon
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is:
To assess the pharmacokinetics of the hydrocodone bitartrate extended-release tablet in subjects with moderate hepatic impairment and in subjects with normal hepatic function.
To assess the safety and tolerability of the hydrocodone bitartrate extended-release tablet in subjects with moderate hepatic impairment and in subjects with normal hepatic function.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatic Impairment
Keywords
Pharmacokinetics, Hydrocodone, Extended Release, Hepatic impairment
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
16 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Normal Hepatic Function
Arm Type
Experimental
Arm Description
Intervention Drug: Hydrocodone bitartrate extended-release tablet
Arm Title
Moderate Hepatic Impairment
Arm Type
Experimental
Arm Description
Intervention Drug: Hydrocodone bitartrate extended-release tablet
Intervention Type
Drug
Intervention Name(s)
Hydrocodone bitartrate extended-release tablet
Intervention Description
15 mg (single dose)
Primary Outcome Measure Information:
Title
Pharmacokinetics (AUC and Cmax) after a single dose
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Safety (occurrence of adverse events, labs, ECG, physical exam, vital signs, oxygen saturation)
Time Frame
throughout the 37 day study period (includes screening, drug administration and pharmacokinetics sampling period, and follow-up)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All subjects:
Written informed consent is obtained
Subjects with normal hepatic function:
The subject is in generally good health (age-appropriate) as determined by medical and psychiatric history, physical examination, ECG, serum chemistry, hematology, coagulation, urinalysis, and serology.
Subjects with hepatic impairment:
The subject's health is otherwise clinically stable as determined by medical history, physical examination, ECG, serum chemistry, hematology, coagulation parameters (PT, activated partial thromboplastin time [aPTT], and international normalized ratio [INR]), urinalysis, and serology except for those signs and symptoms attributable to liver disease.
The subject has case record notes demonstrating physical signs consistent with 1 or more of the following characteristic clinical manifestations of liver cirrhosis: liver firmness to palpation, splenic enlargement, spider angiomas, palmar erythema, parotid hypertrophy, testicular atrophy, ascites (accumulation of fluid in the abdominal cavity), or gynecomastia.
The subject has a Child-Pugh Classification score of 7-9 points (moderate).
Exclusion Criteria:
All subjects:
The subject has any clinically significant, uncontrolled medical condition.
The subject is a poor metabolizer of CYP2D6 substrates based on genotyping performed at screening.
The subject has previously participated in a study with CEP-33237.
The subject has a known sensitivity or idiosyncratic reaction to hydrocodone or hydromorphone, related compounds, or to any metabolites, or any compound listed as being present in a study formulation.
Subjects with normal hepatic function:
The subject has a positive test result for HBsAg or antibodies to hepatitis C.
The subject has a history of alcohol, narcotic, or any other substance abuse.
Subjects with hepatic impairment:
The subject has severe ascites.
The subject has an acute exacerbation of liver disease as indicated by worsening clinical signs of hepatic impairment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sponsor's Medical Expert
Organizational Affiliation
Cephalon, Inc.
Official's Role
Study Director
Facility Information:
Facility Name
Orlando Clinical Research
City
Orlando
State/Province
Florida
ZIP/Postal Code
32809
Country
United States
12. IPD Sharing Statement
Learn more about this trial
A Study to Evaluate the Pharmacokinetics of the Hydrocodone Extended-Release Tablet (CEP-33237) in Subjects With Normal Hepatic Function and Subjects With Moderate Hepatic Impairment
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