The Journal of Pain
Volume 11, Issue 10 , Pages 972-982, October 2010

A Multicenter, Randomized, Double-Blind, Controlled Dose Finding Study of NGX-4010, a High-Concentration Capsaicin Patch, for the Treatment of Postherpetic Neuralgia

  • Lynn R. Webster

      Affiliations

    • Lifetree Clinical Research and Pain Clinic, Salt Lake City, Utah
    • Corresponding Author InformationAddress reprint requests to Lynn R. Webster, M.D., LifeTree Clinical Research, 3838 South 700 East, Suite 202, Salt Lake City, UT 84106.
  • ,
  • T. Philip Malan

      Affiliations

    • University of Arizona, Department of Anesthesiology, Tucson, Arizona
  • ,
  • Michael M. Tuchman

      Affiliations

    • Palm Beach Neurological Center, Palm Beach Gardens, Florida
  • ,
  • Martin D. Mollen

      Affiliations

    • Arizona Research Center, Phoenix, Arizona
  • ,
  • Jeffrey K. Tobias

      Affiliations

    • NeurogesX, Inc., San Mateo, California
  • ,
  • Geertrui F. Vanhove

      Affiliations

    • NeurogesX, Inc., San Mateo, California

Received 22 September 2009; received in revised form 21 December 2009; accepted 15 January 2010. published online 26 July 2010.

Abstract 

Postherpetic neuralgia (PHN) is a painful complication of acute herpes zoster. This multicenter, double-blind, controlled study randomized 299 PHN patients to receive either NGX-4010, a high-concentration capsaicin (8%) patch, or a low-concentration capsaicin (0.04%) control patch for 30, 60, or 90 minutes. The mean percent reductions in NPRS score from baseline to weeks 2 through 8 were significantly greater in the total NGX-4010 group (26.5%, P = .0286) and the 90-minute NGX-4010 group (27.8%, P = .0438) compared to the pooled control group (17.3%). After review of the data suggested a difference between genders in reporting of pain scores and a higher proportion of males (61%) in the 60-minute NGX-4010 group, post hoc gender-stratified analyses were performed and showed that the 60-minute NGX-4010 group also had a significantly larger mean percent reduction in average pain scores (28.0%, P = .0331). Pain reduction in the 30-minute NGX-4010 group, although similar in magnitude to the other doses, was not significantly different from control in either of these analyses. Similar results were observed during weeks 2 through 12. Most treatment-emergent adverse events were application-site specific, transient and mostly mild to moderate in severity.

Perspective

This article reports the safety and efficacy of NGX-4010 applied for 3 different durations (30, 60, or 90 minutes) in patients with PHN. The results identified the 60-minute duration as the dose to be evaluated in subsequent studies and identified a gender effect on reported changes in pain.

Key words: Neuropathic pain, postherpetic neuralgia, capsaicin

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 Funding for this study was provided by NeurogesX.

PII: S1526-5900(10)00296-8

doi:10.1016/j.jpain.2010.01.270

The Journal of Pain
Volume 11, Issue 10 , Pages 972-982, October 2010