A phase 2a, randomized, crossover trial of gabapentin enacarbil for the treatment of postherpetic neuralgia in gabapentin inadequate responders

Abstract

Objective: To compare the efficacy of high-dose (3,600mg/day) vs low-dose (1,200mg/day) oral gabapentin enacarbil (GEn) on pain intensity in adults with postherpetic neuralgia (PHN) and a history of inadequate response to ≥1,800mg/day gabapentin. Design: Multicenter, randomized, double-blind, crossover study (NCT00617461). Setting: Thirty-five outpatient centers in Germany and the United States. Subjects: Subjects aged ≥18 years with a diagnosis of PHN. Methods: During a 2-week baseline period, subjects received open-label treatment with 1,800mg/day gabapentin. Subjects who had a mean 24-hour average pain intensity score ≥4 during the last 7 days of the baseline period were randomized to receive GEn (1,200 or 3,600mg/day) for treatment period 1 (28 days), followed by GEn 2,400mg/day (4 days), and the alternate GEn dose for treatment period 2 (28 days). Results: There was a modest but significant improvement in pain intensity scores with GEn 3,600mg vs 1,200mg (adjusted mean [90% confidence interval] treatment difference, -0.29 [-0.48 to -0.10]; P=0.013). The difference in efficacy between doses was observed primarily in subjects who received the higher dose during treatment period 2; certain aspects of the study design may have contributed to this outcome. Plasma steady-state gabapentin exposure during GEn treatment was as expected and consistent between treatment periods. No new safety signals or adverse event trends relating to GEn exposure were identified. Conclusions: While the overall results demonstrated efficacy in a PHN population, the differences between treatment periods confound the interpretation. These findings could provide insight into future trial designs. © 2013.