mdlinx mdlinx

Randomized, double-blind, placebo-controlled study of the abuse potential of different formulations of oral oxycodone Pain Medicine, 05/11/2012

Webster LR et al. – Intact, orally administered oxycodonecontrolled release (CR) produced less drug liking and high than immediate release (IR) oxycodone, and required approximately twofold greater doses to produce subjective effects comparable to IR oxycodone.

Methods
  • The participants completed an 8–day, placebo–controlled trial with four phases: naloxone challenge, double–blind drug discrimination, double–blind abuse liability, and discontinuation.
  • Nineteen healthy, male, recreational drug abusers participated in this study.
  • The participants were administered different doses and formulations of oxycodone (40 mg immediate release [IR], 40 mg controlled release [CR], crushed 40 mg CR, and 80 mg CR) to evaluate pharmacokinetic parameters and ratings of drug liking and high.
  • Pharmacokinetic parameters were determined over a 12–hour dosing interval.
  • The primary pharmacodynamic endpoints were two questions from the Drug Effects Questionnaire (“Do you like the drug?” and “How high are you now?”).

Results
  • Maximal plasma concentrations and area under the curve determinations were similar for 40 mg IR, crushed 40 mg CR, and 80 mg CR, which were all greater than 40 mg CR.
  • For drug liking and high, the maximal effect and area under the effect curve were similar for the three formulations, which were all greater than 40 mg CR.
  • The dose required to produce comparable reports of drug liking and high was approximately twofold greater for the CR vs IR formulation.
  • When the 40 mg CR tablet was crushed, the pharmacokinetic and pharmacodynamic profile was similar to the 40 mg IR formulation.
  • Adverse events were consistent with opioid administration.

Read this article on Pain Medicine



Register now to view all the MDLinx contents (FREE)!

  • Stay current on the latest literature, research and clinical news
  • Get special communications and offers from MDLinx and our sponsors
  • Receive invitations to paid market research
View Samples and Register

Stay current - Media Tool

Newsletter
RSS
Follow Us
Facebook

Receive free subspecialty
"5-minute updates" via email

Sign up!

Send the E-mail Newsletter to a Colleague


Send

Subscribe to our free RSS feeds:
Get the latest news in your specialty automatically added to your newsreader or your personal My Yahoo!, Google, My MSN or My AOL page. Learn More

Follow Us on Twitter
Twitter is a rich source of instantly updated information. Join today and follow @MDLinx to start receiving tweets. Learn More

Close