Efficacy, safety, and tolerability of NGX-4010, capsaicin 8% patch, in an open-label study of patients with peripheral neuropathic pain

被引:29
|
作者
Webster, Lynn R. [1 ]
Peppin, John F. [2 ]
Murphy, Frederick T. [3 ]
Lu, Biao [4 ]
Tobias, Jeffrey K. [4 ]
Vanhove, Geertrui F. [4 ]
机构
[1] Lifetree Clin Res & Pain Clin, Salt Lake City, UT USA
[2] Pain Treatment Ctr Bluegrass, Lexington, KY USA
[3] Altoona Ctr Clin Res, Duncansville, PA USA
[4] NeurogesX Inc, San Mateo, CA USA
关键词
Peripheral neuropathic pain; Painful diabetic neuropathy; Postherpetic neuralgia; Capsaicin patch; POSTHERPETIC NEURALGIA; TOPICAL CAPSAICIN; DOUBLE-BLIND; HERPES-ZOSTER; PHARMACOLOGICAL MANAGEMENT; DIABETIC-NEUROPATHY; EFNS GUIDELINES; RECEPTOR TRPV1; DERMAL PATCH; EPIDEMIOLOGY;
D O I
10.1016/j.diabres.2011.04.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To assess efficacy, safety, and tolerability of NGX-4010, capsaicin 8% patch, in patients with peripheral neuropathic pain. Methods: This open-label, uncontrolled, 12-week study enrolled 25 patients with postherpetic neuralgia (PHN), one with HIV-distal sensory polyneuropathy, and 91 with painful diabetic neuropathy (PDN). Patients received pre-treatment with one of three 4% lidocaine topical anesthetics (L.M.X.4(1), Topicaine Gel(2), or Betacaine Enhanced Gel 4(3)) followed by a single 60- or 90-min NGX-4010 application. The primary efficacy variable was the percentage change in Numeric Pain Rating Scale scores from baseline to Weeks 2-12. Adverse events (AEs), laboratory parameters, vital signs, neurosensory examinations, dermal assessments, treatment-related pain scores, and medication use for treatment-related pain were collected. Results: PDN and PHN patients achieved a 31% and 28% mean pain decrease from baseline during Weeks 2-12, respectively, and 47% and 44%, respectively, were responders (>= 30% pain decrease). Mild or moderate treatment-site-related burning and pain were the most common AEs and there was no evidence of impaired neurosensory function. Conclusions: NGX-4010 in conjunction with any of the three topical anesthetics tested was generally safe and well tolerated and reduced pain over a 12-week period in patients with PDN and PHN. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:187 / 197
页数:11
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