Controlled Study of NGX-4010 for the Treatment of Postherpetic Neuralgia

NCT ID: NCT00068081

Last Updated: 2008-03-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 150 participants
• Study Classification: INTERVENTIONAL

Brief Summary

The purpose of the study is to assess the efficacy, safety and tolerability of NGX 4010 applied for 60 minutes for the treatment of PHN.

Conditions

Herpes Zoster; Neuralgia; Pain; Peripheral Nervous System Diseases

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

Capsaicin Dermal Patch

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• At least 18 years of age.
• Be in good health.
• Diagnosis of postherpetic neuralgia (PHN) made by the primary treating physician or Investigator, and at least 3 months post-vesicle crusting.
• Screening Pain Sum Score of 12 to 36.
• Intact, unbroken skin over the painful area(s) to be treated.
• If taking chronic pain medications, be on a stable (not PRN) regimen for at least 21 days prior to Treatment Visit (Day 0) and willing to maintain medications at same stable dose(s) and schedule throughout the study.
• Female subjects with child-bearing potential must have a negative serum beta hCG pregnancy test, to be performed at the Screening Visit.
• All subjects must be willing to use effective methods of birth control and/or refrain from participating in a conception process during the study and for 30 days following experimental drug exposure.
• Be willing and able to comply with protocol requirements for the duration of study participation. (Such requirements include, but are not limited to: completing a daily pain diary, attending all study visits, and refraining from elective surgery and extensive travel during study participation.)

Exclusion Criteria

• Concomitant opioid medication, unless orally or transdermally administered and not exceeding a total daily dose of morphine 60 mg/day, or equivalent. Parenteral opioid use is excluded, regardless of dose.
• Unavailability of an effective rescue medication strategy for the subject, such as unwillingness to use opioid analgesics during treatment, or high tolerance to opioids precluding the ability to relieve treatment-associated discomfort with Roxicodone®, as judged by the Investigator.
• Active substance abuse or history of chronic substance abuse within the past year, or prior chronic substance abuse judged likely to recur during the study period by the investigator.
• Recent use (within 21 days preceding the Treatment Visit [Day 0]) of any topically applied pain medication, such as non-steroidal anti-inflammatory drugs, menthol, methyl salicylate, local anesthetics (including Lidoderm®), steroids or capsaicin products on the painful areas.
• Current use of any investigational agent, or Class 1 anti-arrhythmic drugs (such as tocainide and mexiletine).
• Significant pain of an etiology other than PHN, for example, compression-related neuropathies (e.g., spinal stenosis) or fibromyalgia or arthritis. Subjects must not have significant ongoing pain from other cause(s) that may interfere with judging PHN-related pain.
• Painful PHN areas located only on the face, above the hairline of the scalp, and/or in proximity to mucous membranes. (Investigational treatment with NGX-4010 is not allowed in these areas.)
• Any implanted medical device (spinal cord stimulator, intrathecal pump or peripheral nerve stimulator) for the treatment of neuropathic pain.
• Hypersensitivity to capsaicin (i.e., chili peppers or Over-the-Counter (OTC) capsaicin products), local anesthetics, Roxicodone® or adhesives.
• Significant ongoing or untreated abnormalities in cardiac, renal, hepatic, or pulmonary function that may interfere either with the ability to complete the study or the evaluation of adverse events.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

NeurogesX

INDUSTRY

Sponsor Role: lead

Locations

NeurogesX Investigational Site

Mesa, Arizona, United States

NeurogesX Investigational Site

Peoria, Arizona, United States

NeurogesX Investigational Site

Phoenix, Arizona, United States

NeurogesX Investigational Site

Duarte, California, United States

NeurogesX Investigational Site

Santa Rosa, California, United States

NeurogesX Investigational Site

Boynton Beach, Florida, United States

NeurogesX Investigational Site

Bradenton, Florida, United States

NeurogesX Investigational Site

Fort Myers, Florida, United States

NeurogesX Investigational Site

Naples, Florida, United States

NeurogesX Investigational Site

Tampa, Florida, United States

NeurogesX Investigational Site

Atlanta, Georgia, United States

NeurogesX Investigational Site

Marietta, Georgia, United States

NeurogesX Investigational Site

Brighton, Massachusetts, United States

NeurogesX Investigational Site

St Louis, Missouri, United States

NeurogesX Investigational Site

St Louis, Missouri, United States

NeurogesX Investigational Site

Winston-Salem, North Carolina, United States

NeurogesX Investigational Site

Dallas, Texas, United States

NeurogesX Investigational Site

San Antonio, Texas, United States

NeurogesX Investigational Site

Salt Lake City, Utah, United States

Countries

United States

References

Webster LR, Tark M, Rauck R, Tobias JK, Vanhove GF. Effect of duration of postherpetic neuralgia on efficacy analyses in a multicenter, randomized, controlled study of NGX-4010, an 8% capsaicin patch evaluated for the treatment of postherpetic neuralgia. BMC Neurol. 2010 Oct 11;10:92. doi: 10.1186/1471-2377-10-92.

Reference Type: DERIVED

PMID: 20937130 (View on PubMed)

Other Identifiers

C110

Identifier Type: -

Identifier Source: org_study_id