Long-Term Safety of NGX-4010, a High-Concentration Capsaicin Patch, in Patients with Peripheral Neuropathic Pain

被引:69
作者
Simpson, David M. [1 ]
Gazda, Suzanne [2 ]
Brown, Stephen [3 ]
Webster, Lynn R. [4 ]
Lu, Shiao-Ping [5 ]
Tobias, Jeffrey K. [5 ]
Vanhove, Geertrui F. [5 ]
机构
[1] Mt Sinai Med Ctr, Mt Sinai Sch Med, Clin Neurophysiol Labs, Dept Neurol, New York, NY 10029 USA
[2] Integra Clin Res, San Antonio, TX USA
[3] AIDS Res Alliance, Los Angeles, CA USA
[4] Lifetree Clin Res & Pain Clin, Salt Lake City, UT USA
[5] NeurogesX Inc, San Mateo, CA USA
关键词
Peripheral neuropathic pain; posthopetic neuralgia; HIV-associated distal sensory polyneuropathy; capsaicin; POSTHERPETIC NEURALGIA; TOPICAL CAPSAICIN; HIV NEUROPATHY; CONTROLLED-TRIAL; EPIDEMIOLOGY; MANAGEMENT; UPDATE; ZOSTER;
D O I
10.1016/j.jpainsymman.2009.11.316
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Context. Postherpetic neuralgia (PHN) and painful human immunodeficiency virus-associated distal sensory polyneuropathy (HIV-DSP) are peripheral neuropathic pain syndromes that are difficult to treat. Current treatment options are often limited by poor tolerability. Objectives. The objective of the current open-label study was to assess the safety of repeated applications of NGX-4010, a high-concentration capsaicin patch (capsaicin 8%), over one year, in patients with moderate to severe PHN or HIV-DSP. Methods. Patients had successfully completed a previous NGX-4010 study and had a pain level appropriate for further treatment. Eligible patients had not been treated with NGX-4010 within 12 weeks of study initiation. Patients received pretreatment with a topical local anesthetic (lidocaine 4%) for 60 minutes followed by either a 60-minute (PHN and HIV-DSP patients) or a 90-minute (HIV-DSP patients) treatment with NGX-4010. Patients could receive up to three additional treatments at intervals of >= 12 weeks. Regardless of the number of treatments received, all patients were followed up for 48 weeks except for those withdrawing early. Results. A total of 106 patients were enrolled and received a total of 293 NGX-4010 treatments. The most frequently reported treatment-emergent adverse events were transient, mild-to-moderate application site erythema, pain, edema, and papules. Small, transient pain-related increases in blood pressure during and immediately after NGX4010 application were observed. There was no evidence of an increased incidence of adverse events, dermal irritation, intolerability, or impaired neurological function with repeated treatments. Conclusion. It is concluded that repeated treatments with NGX-4010 administered over a one-year period are generally safe and well tolerated. J Pain Symptom Manage 2010;39:1053-1064. (C) 2010 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1053 / 1064
页数:12
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