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Aprepitant Effects on Oxycodone Response

Primary Purpose

Narcotic Abuse

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Aprepitant 0mg
Aprepitant 40mg
Aprepitant 200mg
Oxycodone 0mg, p.o.
Oxycodone 20mg, p.o.
Oxycodone 40mg, p.o.
Oxycodone 0mg, IN
Oxycodone 15mg, IN
Oxycodone 30mg, IN
Sponsored by
Sharon Walsh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Narcotic Abuse focused on measuring opioid, oxycodone, NK1 antagonist, aprepitant, intranasal, abuse

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Recreational user of opioids
  • Healthy
  • Ages 18-55 years old
  • Able to provide informed consent

Exclusion Criteria:

  • Ongoing medical or psychiatric condition that would be contraindicated for participation
  • Past 30 day use of and P4503A4 inhibitor

Sites / Locations

  • University of Kentucky

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm 9

Arm 10

Arm 11

Arm 12

Arm 13

Arm 14

Arm 15

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Placebo aprepitant/0 mg oxycodone IN PO

Placebo aprepitant/ oxycodone 15 IN 0 PO

Placebo aprepitant/ oxycodone 30 IN 0 PO

Placebo aprepitant/ oxycodone 0 IN 20 PO

Placebo aprepitant/ oxycodone 0 IN 40 PO

Aprepitant 40 mg/ oxycodone 0 IN 0 PO

Aprepitant 40 mg/ oxycodone 0 IN 20 PO

Aprepitant 40 mg/ oxycodone 0 IN 40 PO

Aprepitant 40 mg/ oxycodone 15 IN 0 PO

Aprepitant 40 mg/ oxycodone 30 IN 0 PO

Aprepitant 200 mg/ oxycodone 0 IN 0 PO

Aprepitant 200 mg/ oxycodone 0 IN 20 PO

Aprepitant 200 mg/ oxycodone 0 IN 40 PO

Aprepitant 200 mg/ oxycodone 15 IN 0 PO

Aprepitant 200 mg/ oxycodone 30 IN 0 PO

Arm Description

Placebo aprepitant/Placebo oxycodone IN/PO

Placebo aprepitant/ oxycodone 15 IN 0 PO

Placebo aprepitant/ oxycodone 30 IN 0 PO

Placebo aprepitant/ oxycodone 0 IN 20 PO

Placebo aprepitant/ oxycodone 0 IN 40 PO

Aprepitant 40 mg/ oxycodone 0 IN 0 PO

Aprepitant 40 mg/ oxycodone 0 IN 20 PO

Aprepitant 40 mg/ oxycodone 0 IN 40 PO

Aprepitant 40 mg/ oxycodone 15 IN 0 PO

Aprepitant 40 mg/ oxycodone 30 IN 0 PO

Aprepitant 200 mg/ oxycodone 0 IN 0 PO

Aprepitant 200 mg/ oxycodone 0 IN 20 PO

Aprepitant 200 mg/ oxycodone 0 IN 40 PO

Aprepitant 200 mg/ oxycodone 15 IN 0 PO

Aprepitant 200 mg/ oxycodone 30 IN 0 PO

Outcomes

Primary Outcome Measures

Abuse Liability Proxy
Visual analog scale ratings (from 0-100) on the subject-rated measure of "How much do you like the drug?" with higher scores indicating greater abuse liability (and 100 anchored with "extremely" and zero indicating none anchored with "none at all." Data were collected across multiple time points but the peak maximum score was used for the primary outcome measure.

Secondary Outcome Measures

Respiration Depression
Respiration rate measured over 60 seconds. Data were collected across multiple time points, but the peak minimum score was used for this outcome measure.

Full Information

First Posted
October 20, 2009
Last Updated
August 3, 2017
Sponsor
Sharon Walsh
Collaborators
National Institute on Drug Abuse (NIDA), Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00999544
Brief Title
Aprepitant Effects on Oxycodone Response
Official Title
New Neural Drug Targets: An Evaluation of the Effects of Aprepitant on the Response to Oxycodone
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
April 2011 (Actual)
Study Completion Date
April 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sharon Walsh
Collaborators
National Institute on Drug Abuse (NIDA), Merck Sharp & Dohme LLC

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Addressing the issue of opioid dependence and tolerance has public health implications for the treatment of opioid abuse (both heroin as well as pharmaceutical opioids) and for the treatment of pain. Recent preclinical data suggest a role for Substance P (NK-1) receptors in modulating both the acute and chronic response to opioids. The objective of this study is to determine whether pretreatment with aprepitant, a selective neurokinin-1 (NK-1) antagonist can reduce the direct response to an opioid agonist (oxycodone) on measures related to abuse liability and reinforcing effects.
Detailed Description
Healthy adult volunteers with histories of illicit opioid use by the intranasal and oral routes will be admitted to this 6-week inpatient, crossover study. They will participate in 15 experimental test sessions, each lasting approximately 6.5 hours, during which they will receive a range of acute doses of aprepitant, including placebo, followed by challenge with oxycodone or placebo (given intranasally or orally). Multi-dimensional outcomes, including physiological (blood pressure, oxygen saturation, pupil diameter), subjective (questionnaires related to mood, abuse liability) and observer ratings will be collected repeatedly throughout each session. Data will be analyzed using parametric approaches to within-subject designs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Narcotic Abuse
Keywords
opioid, oxycodone, NK1 antagonist, aprepitant, intranasal, abuse

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Within subject crossover designed that examined 15 experimental conditions within a single group of participants
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo aprepitant/0 mg oxycodone IN PO
Arm Type
Experimental
Arm Description
Placebo aprepitant/Placebo oxycodone IN/PO
Arm Title
Placebo aprepitant/ oxycodone 15 IN 0 PO
Arm Type
Experimental
Arm Description
Placebo aprepitant/ oxycodone 15 IN 0 PO
Arm Title
Placebo aprepitant/ oxycodone 30 IN 0 PO
Arm Type
Experimental
Arm Description
Placebo aprepitant/ oxycodone 30 IN 0 PO
Arm Title
Placebo aprepitant/ oxycodone 0 IN 20 PO
Arm Type
Experimental
Arm Description
Placebo aprepitant/ oxycodone 0 IN 20 PO
Arm Title
Placebo aprepitant/ oxycodone 0 IN 40 PO
Arm Type
Experimental
Arm Description
Placebo aprepitant/ oxycodone 0 IN 40 PO
Arm Title
Aprepitant 40 mg/ oxycodone 0 IN 0 PO
Arm Type
Experimental
Arm Description
Aprepitant 40 mg/ oxycodone 0 IN 0 PO
Arm Title
Aprepitant 40 mg/ oxycodone 0 IN 20 PO
Arm Type
Experimental
Arm Description
Aprepitant 40 mg/ oxycodone 0 IN 20 PO
Arm Title
Aprepitant 40 mg/ oxycodone 0 IN 40 PO
Arm Type
Experimental
Arm Description
Aprepitant 40 mg/ oxycodone 0 IN 40 PO
Arm Title
Aprepitant 40 mg/ oxycodone 15 IN 0 PO
Arm Type
Experimental
Arm Description
Aprepitant 40 mg/ oxycodone 15 IN 0 PO
Arm Title
Aprepitant 40 mg/ oxycodone 30 IN 0 PO
Arm Type
Experimental
Arm Description
Aprepitant 40 mg/ oxycodone 30 IN 0 PO
Arm Title
Aprepitant 200 mg/ oxycodone 0 IN 0 PO
Arm Type
Experimental
Arm Description
Aprepitant 200 mg/ oxycodone 0 IN 0 PO
Arm Title
Aprepitant 200 mg/ oxycodone 0 IN 20 PO
Arm Type
Experimental
Arm Description
Aprepitant 200 mg/ oxycodone 0 IN 20 PO
Arm Title
Aprepitant 200 mg/ oxycodone 0 IN 40 PO
Arm Type
Experimental
Arm Description
Aprepitant 200 mg/ oxycodone 0 IN 40 PO
Arm Title
Aprepitant 200 mg/ oxycodone 15 IN 0 PO
Arm Type
Experimental
Arm Description
Aprepitant 200 mg/ oxycodone 15 IN 0 PO
Arm Title
Aprepitant 200 mg/ oxycodone 30 IN 0 PO
Arm Type
Experimental
Arm Description
Aprepitant 200 mg/ oxycodone 30 IN 0 PO
Intervention Type
Drug
Intervention Name(s)
Aprepitant 0mg
Intervention Description
Aprepitant 0mg, p.o. pretreatment
Intervention Type
Drug
Intervention Name(s)
Aprepitant 40mg
Intervention Description
Aprepitant 40mg, p.o. pretreatment
Intervention Type
Drug
Intervention Name(s)
Aprepitant 200mg
Intervention Description
Aprepitant 200mg, p.o. pretreatment
Intervention Type
Drug
Intervention Name(s)
Oxycodone 0mg, p.o.
Intervention Description
Oxycodone 0mg, p.o.
Intervention Type
Drug
Intervention Name(s)
Oxycodone 20mg, p.o.
Intervention Description
Oxycodone 20mg, p.o.
Intervention Type
Drug
Intervention Name(s)
Oxycodone 40mg, p.o.
Intervention Description
Oxycodone 40mg, p.o.
Intervention Type
Drug
Intervention Name(s)
Oxycodone 0mg, IN
Intervention Description
Oxycodone 0mg, IN
Intervention Type
Drug
Intervention Name(s)
Oxycodone 15mg, IN
Intervention Description
Oxycodone 15mg, IN
Intervention Type
Drug
Intervention Name(s)
Oxycodone 30mg, IN
Intervention Description
Oxycodone 30mg, IN
Primary Outcome Measure Information:
Title
Abuse Liability Proxy
Description
Visual analog scale ratings (from 0-100) on the subject-rated measure of "How much do you like the drug?" with higher scores indicating greater abuse liability (and 100 anchored with "extremely" and zero indicating none anchored with "none at all." Data were collected across multiple time points but the peak maximum score was used for the primary outcome measure.
Time Frame
42 days
Secondary Outcome Measure Information:
Title
Respiration Depression
Description
Respiration rate measured over 60 seconds. Data were collected across multiple time points, but the peak minimum score was used for this outcome measure.
Time Frame
42 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Recreational user of opioids Healthy Ages 18-55 years old Able to provide informed consent Exclusion Criteria: Ongoing medical or psychiatric condition that would be contraindicated for participation Past 30 day use of and P4503A4 inhibitor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sharon L Walsh, Ph.D.
Organizational Affiliation
University of Kentucky
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Kentucky
City
Lexington
State/Province
Kentucky
ZIP/Postal Code
40502
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22260216
Citation
Walsh SL, Heilig M, Nuzzo PA, Henderson P, Lofwall MR. Effects of the NK1 antagonist, aprepitant, on response to oral and intranasal oxycodone in prescription opioid abusers. Addict Biol. 2013 Mar;18(2):332-43. doi: 10.1111/j.1369-1600.2011.00419.x. Epub 2012 Jan 19.
Results Reference
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Aprepitant Effects on Oxycodone Response

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