A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 in Subjects With Postherpetic Neuralgia and Post-Trau...

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Reference: EUCTR2008-007478-39

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy, Safety, and Tolerability of JNJ-42160443 in Subjects With Postherpetic Neuralgia and Post-Traumatic Neuralgia, Followed by a Double Blind Safety Extension and an Open-Label Safety Extension

Woman and Man

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Extract

• To evaluate the analgesic efficacy of JNJ-42160443 (1, 3, and 10 mg; administered as a single, subcutaneous injection every 28 days) in reducing average pain intensity, in subjects with postherpetic neuralgia • To evaluate the safety and tolerability of multiple doses of JNJ-42160443 (1, 3, and 10 mg), when administered as a single, subcutaneous injection every 28 days to subjects with postherpetic neuralgia for up to 2 years


Inclusion criteria

  • Postherpetic Neuralgia and Post-Traumatic Neuralgia