Clinical Drug Investigation

, Volume 30, Issue 8, pp 489–505 | Cite as

Efficacy and Safety of Tapentadol Extended Release Compared with Oxycodone Controlled Release for the Management of Moderate to Severe Chronic Pain Related to Osteoarthritis of the Knee

A Randomized, Double-Blind, Placebo- and Active-Controlled Phase III Study
  • Marc Afilalo
  • Mila S. EtropolskiEmail author
  • Brigitte Kuperwasser
  • Kathy Kelly
  • Akiko Okamoto
  • Ilse Van Hove
  • Achim Steup
  • Bernd Lange
  • Christine Rauschkolb
  • Juergen Haeussler
Original Research Article


Background: Tapentadol is a novel, centrally acting analgesic with μ-opioid receptor agonist and norepinephrine reuptake inhibitor activity.

Objective: To evaluate the efficacy and safety of tapentadol extended release (ER) compared with oxycodone controlled release (CR) for management of moderate to severe chronic osteoarthritis-related knee pain.

Methods: This was a randomized, double-blind, active- and placebo-controlled, parallel-arm, multicentre, phase III study during which patients received tapentadol ER, oxycodone CR or placebo for a 3-week titration period followed by a 12-week maintenance period. The study was carried out at sites in Australia, Canada, New Zealand and the US. A total of 1030 patients with chronic osteoarthritis-related knee pain were randomized to receive tapentadol ER 100–250 mg twice daily, oxycodone HCl CR 20–50 mg twice daily or placebo. Primary endpoints (as determined prior to initiation of the study) were the changes from baseline in average daily pain intensity (rated by patients on an 11-point numerical rating scale) over the last week of maintenance and over the entire 12-week maintenance period; last observation carried forward was used to impute missing values after early treatment discontinuation.

Results: Efficacy and safety were evaluated for 1023 patients. Tapentadol ER significantly reduced average pain intensity from baseline to week 12 of the maintenance period versus placebo (least squares mean [LSM] difference [95% CI], −0.7 [−1.04, −0.33]), and throughout the maintenance period (−0.7 [−1.00, −0.33]). Oxycodone CR significantly reduced average pain intensity from baseline throughout the maintenance period versus placebo (LSM difference [95% CI], −0.3 [−0.67, −0.00]) but not at week 12 (−0.3 [−0.68, 0.02]). A significantly higher percentage of patients achieved ≥50% improvement in pain intensity in the tapentadol ER group (32.0% [110/344]) compared with the placebo group (24.3% [82/337]; p = 0.027), indicating a clinically significant improvement in pain intensity, while a significantly lower percentage of patients achieved ≥50% improvement in pain intensity in the oxycodone CR group (17.3% [59/342]; p = 0.023 vs placebo). In the placebo, tapentadol ER and oxycodone CR groups, respectively, 61.1% (206/337), 75.9% (261/344) and 87.4% (299/342) of patients reported at least one treatment-emergent adverse event (TEAE); incidences of gastrointestinal-related TEAEs were 26.1% (88/337), 43.0% (148/344) and 67.3% (230/342).

Conclusion: Treatment with tapentadol ER 100–250 mg twice daily or oxycodone HCl CR 20–50 mg twice daily was effective for the management of moderate to severe chronic osteoarthritis-related knee pain, with substantially lower incidences of gastrointestinal-related TEAEs associated with treatment with tapentadol ER than with oxycodone CR. [Trial registration number: NCT00421928 ( Identifier)]


Oxycodone Less Square Mean Maintenance Period Tapentadol Opioid Withdrawal 
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This study was funded by Johnson & Johnson Pharmaceutical Research & Development, L.L.C. M. Afilalo received funding for study support from Johnson & Johnson Pharmaceutical Research & Development, L.L.C. M. Etropolski, B. Kuperwasser, K. Kelly, A. Okamoto, I. Van Hove, C. Rauschkolb, and J. Haeussler are Johnson & Johnson employees and shareholders. A. Steup and B. Lange are employees of Grünenthal GmbH. Editorial support for the writing of this manuscript was provided by Cherie Koch, PhD, of MedErgy, and was funded by Johnson & Johnson Pharmaceutical Services, L.L.C., and Grünenthal GmbH. M. Afilalo, who is not employed by Johnson & Johnson Pharmaceutical Services, L.L.C., or Grünenthal GmbH, was not compensated for his contribution to the writing of this manuscript and has no conflicts of interest that are directly relevant to the content of this study. Although writing assistance was provided, the authors retained full editorial control over the content of the manuscript.


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Copyright information

© Adis Data Information BV 2010

Authors and Affiliations

  • Marc Afilalo
    • 1
  • Mila S. Etropolski
    • 2
    Email author
  • Brigitte Kuperwasser
    • 2
  • Kathy Kelly
    • 2
  • Akiko Okamoto
    • 2
  • Ilse Van Hove
    • 3
  • Achim Steup
    • 4
  • Bernd Lange
    • 4
  • Christine Rauschkolb
    • 2
  • Juergen Haeussler
    • 2
  1. 1.Sir Mortimer B. Davis Jewish General HospitalMontrealCanada
  2. 2.Johnson & Johnson Pharmaceutical Research & DevelopmentL.L.C.RaritanUSA
  3. 3.Johnson & Johnson Pharmaceutical Research & DevelopmentDivision of Janssen PharmaceuticaN.V.Belgium
  4. 4.Global DevelopmentGrünenthal GmbHAachenGermany

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