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Mirogabalin for the management of postherpetic neuralgia

a randomized, double-blind, placebo-controlled phase 3 study in Asian patients

Kato, Jitsua; Matsui, Norimitsub; Kakehi, Yoshihirob,*; Murayama, Emikoc; Ohwada, Shoichid; Sugihara, Masahirod

doi: 10.1097/j.pain.0000000000001501
Research Paper
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SDC

This study investigated the safety and efficacy of mirogabalin, a novel, potent, selective ligand of the α2δ subunit of voltage-dependent Ca2+ channels, for the treatment of postherpetic neuralgia (PHN). In this multicenter, double-blind, placebo-controlled phase 3 study, Asian patients ≥20 years with PHN were randomized 2:1:1:1 to placebo or mirogabalin 15, 20, or 30 mg/day for up to 14 weeks (NCT02318719). The primary efficacy endpoint was the change from baseline in average daily pain score at week 14, defined as a weekly average of daily pain (0 = “no pain” to 10 = “worst possible pain,” for the last 24 hours). Of 765 patients randomized, 763 received ≥ 1 dose of the study drug and were included in the analysis; 303, 152, 153, and 155 received placebo, mirogabalin 15, 20, or 30 mg/day, respectively. A total of 671 (87.7%) patients completed the study. At week 14, the difference in average daily pain score least squares mean vs placebo was −0.41, −0.47, and −0.77, respectively; all mirogabalin groups showed statistical significance. The most common treatment-emergent adverse events were somnolence, nasopharyngitis, dizziness, weight increase, and edema, and all of them were mild or moderate in severity. Mirogabalin was superior to placebo in all groups for relieving PHN and appeared well tolerated.

Mirogabalin has demonstrated a well-balanced profile of efficacy and safety and may provide an alternative therapeutic option for the treatment of postherpetic neuralgia.

aDepartment of Anesthesiology, Nihon University School of Medicine, Tokyo, Japan

bClinical Development Department, Daiichi Sankyo Co, Ltd, Tokyo, Japan

cAsia Development Department, Daiichi Sankyo Co, Ltd, Tokyo, Japan

dBiostatistics and Data Management Department, Daiichi Sankyo Co, Ltd, Tokyo, Japan

Corresponding author. Address: Clinical Development Department, Daiichi Sankyo Co, Ltd, Tokyo, Japan. Tel.: 08010324489. E-mail address: kakehi.yoshihiro.vs@daiichisankyo.co.jp (Y. Kakehi).

Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.

This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

Received August 08, 2018

Received in revised form January 10, 2019

Accepted January 14, 2019

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1. Introduction

Neuropathic pain has many causes, including neuropathy due to diabetes mellitus or to herpes zoster and spinal cord injury. Symptoms of postherpetic neuralgia (PHN) include spontaneous pain, hyperalgesia, and allodynia.

Multiple factors play a role in neuropathic pain, including the involvement of voltage-dependent sodium and calcium channels.11 Animal studies support the role of voltage-dependent Ca2+ channels (VDCCs) in neuropathic pain signaling. In animal studies, the α2δ subunit of VDCCs enhances the activity of VDCCs by enabling increased trafficking to the membrane, leading to increased peripheral and central neuron excitability that is believed to contribute to neuropathic pain.2,16,17 Although the mechanism of action is not fully understood, it is believed that α2δ ligands alleviate neuropathic pain by reducing the enhanced Ca2+ influx and neuronal excitability mediated by the α2δ subunit.2,16,17

Current options for managing neuropathic pain include anticonvulsants, tricyclic antidepressants, and serotonin/norepinephrine reuptake inhibitors. No single class of medication has shown efficacy for all neuropathic pain patients, and studies estimate the effect size reported in meta-analyses of pharmacotherapy for neuropathic pain may have been overestimated.12 Many patients take multiple medications for neuropathic pain, which increases the risk of adverse events (AEs).3 Current guidelines issued by the Japanese Society of Pain Clinicians for the management of neuropathic pain recommend the use of pharmacologic therapies as the best treatment strategy for neuropathic pain that focuses on the improvement of pain and quality of life (QoL).24 Therefore, there is an unmet medical need for a management option with less AEs and high efficacy.

Mirogabalin monobenzenesulfonate (herein referred to as mirogabalin, Daiichi Sankyo Co, Ltd, Tokyo, Japan) is a novel, selective oral α2δ ligand being developed for the treatment of PHN and diabetic peripheral neuropathic pain (DPNP). In contrast to pregabalin, a standard α2δ ligand, mirogabalin showed higher binding affinities in human and rat α2δ subunits; furthermore, it had a slower dissociation rate for the α2δ-1 subunit than the α2δ-2 subunit. When studied in experimental neuropathic pain models, partial sciatic nerve ligation rats, and streptozotocin-induced diabetic rats, mirogabalin showed more potent and longer-lasting analgesic effects.5 A phase 2 trial of mirogabalin has proven the drug's effectiveness in reducing sleep disturbances and improving pain scores associated with DPNP.19,25,26

This phase 3, randomized, double-blind, placebo-controlled study evaluated the efficacy and safety of mirogabalin in Asian patients with PHN.

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2. Research design and methods

2.1. Study design

This was a multicenter, double-blind, placebo-controlled, 14-week, parallel group study for the treatment of PHN (NCT02318719) in Asian patients, conducted between January 23, 2015, and January 9, 2017. This study followed the Declaration of Helsinki and the International Council for Harmonisation Consolidated Guideline E6 for Good Clinical Practice. There were approximately 200 study sites in Japan, Korea, Taiwan, Singapore, Malaysia, and Thailand, and the study was approved by the institutional review board, or equivalent, for each site before beginning. Before enrollment, informed consent was obtained from all patients. Safety was periodically monitored by an independent Data Safety Monitoring Board.

To be eligible for the study, patients had to meet all the following criteria: Asian ≥20 years of age with PHN (defined as persistent pain after 3 months from the disappearance of the herpes zoster rash); able to give written informed consent for study participation, understand procedures of this study, and complete patient-reported questionnaires adequately; a pain scale of ≥40 mm on visual analogue scale (VAS) of Short-form McGill Pain Questionnaire (SF-MPQ) at screening and randomization; and an average daily pain score (ADPS) of ≥4 on the 11-point numeric rating scale (NRS) over the past 7 days.

Patients were excluded if they met any of the following criteria: pain scale ≥90 mm on VAS of SF-MPQ at screening and randomization, or their daily pain score was ≥9 during observation period; previous use of a neurolytic block or neurosurgical therapy for current PHN; severe pain or neurologic disorder at screening or randomization not related to PHN; major psychiatric disorder at screening or randomization; use of prohibited concomitant drugs or prohibited concomitant therapies within 7 days or change of restricted concomitant drugs within 14 days before screening; presence of a skin condition that could complicate the assessment of PHN pain; previous use of pregabalin ≥300 mg/day or gabapentin ≥1200 mg/day with lack of effect or known hypersensitivity; creatinine clearance <60 mL/minute using the Cockcroft–Gault equation; malignancy other than basal cell carcinoma within the past 2 years before screening; clinically significant unstable neurologic, ophthalmologic, hepatobiliary, respiratory, or hematologic illness or unstable cardiovascular disease within 12 months before screening; clinically significant electrocardiogram findings at screening; history of pernicious anemia, untreated hypothyroidism, or HIV infection; known immunocompromised status or history of positive hepatitis B antigen or hepatitis C antibody; in women, pregnancy, potential pregnancy, or breastfeeding; or male or female unwilling to take reliable contraceptive measures during and for 4 weeks after the study; participation in another clinical study within 30 days before informed consent, or participation in any clinical study where mirogabalin was received; abuse of illicit drugs or alcohol within 1 year of screening; “yes” response to any question on the Columbia-Suicide Severity Rating Scale (C-SSRS) at screening or randomization in relation to events occurring within past year; previous treatment with a drug that could cause irreversible retinal degeneration; clinical laboratory values exceeding specified study limits at screening; or a “yes” response to the suicidality question on the Major Depressive Episode Module or to any question of B1b, B3-B11c, B13, or B14 in the Suicidality Module on the Mini-International Neuropsychiatric Interview at screening.

After informed consent, but before the screening visit, patients who received any of the following prohibited concomitant medications underwent a 7-day washout period: pregabalin; antiepileptics; hypnotics and anxiolytics; opioids; tramadol and any of its combination drugs; Neurotropin; N-methyl-D-aspartate receptor antagonists; muscle relaxants; topical capsaicin, steroids, prostaglandins, or local anesthetics, except as topical products for a nondisease site of PHN; sodium channel blockers; centrally acting sympatholytics; vitamin B1 or B12; α-lipoic acid; evening primrose oil; nefopam; immunosuppressants; drugs that could cause irreversible retinal degeneration; and study drugs in other studies. The patients could not resume these medications during the study. Patients could continue taking antidepressants, ultrashortacting hypnotics, nonsteroidal anti-inflammatory drugs, and Chinese herbal medications during the study provided the dosage had not changed for 14 days before screening, and the dosage was not changed and the drug was not stopped unless safety problems were observed.

After informed consent but before the screening visit, patients who received any of the following prohibited concomitant therapies underwent a 7-day washout period: nerve blocks; iontophoresis; laser therapy; acupuncture; spinal cord stimulation; surgery that could confound PHN assessment; transcutaneous electrical nerve stimulation; and other forms of pain reduction therapy for PHN except psychological, mental, and physical therapy. These therapies could not be resumed during the study. Patients could continue psychological, mental, or physical therapies provided the frequency of therapy had not changed from 14 days before the screening visit, and the therapy was not started after the screening visit.

After a 7-day observation period, patients were randomized 2:1:1:1 to 1 of 4 treatment groups: placebo, or mirogabalin 15 mg once daily, 10 mg twice daily, or 15 mg twice daily in accordance with the randomization schedule securely maintained in Interactive Web Response System (Bell Medical Solutions, Inc, Tokyo, Japan). Randomization was stratified by dichotomized baseline ADPS (<6 vs ≥6). The randomization schedule was generated and securely kept by the independent biostatistician of Bell Medical Solutions, Inc, throughout the study to maintain the blinding.

The study consisted of a 1-week observation period, followed by a 1- to 2-week dose titration period, a 12- to 13-week fixed-dose period, and a 1-week follow-up period, where patients were monitored after treatment (Fig. 1). For the mirogabalin 15 mg/day group, 5 mg/day was administered for the first week (once daily at bedtime), followed by 10 mg/day (10 mg once daily) during the second week of the titration period. For the mirogabalin 20- and 30-mg/day groups, 10 mg/day was administered (5 mg twice daily; once in the morning and at bedtime) during the first week of the titration period. On the second week, mirogabalin was administered 20 mg/day (10 mg twice daily; once in the morning and at bedtime) to the 30 mg/day group (15 mg twice daily; once in the morning and once at bedtime). Patients who were randomized to the 15 mg/day group received a matching placebo tablet in the morning. During the study, acetaminophen was permitted as rescue medication, up to the maximum dose in the package insert, as needed; patients were instructed to record in the electronic patient diary the dose of acetaminophen used.

Figure 1

Figure 1

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2.2. Efficacy assessments

The primary efficacy endpoint was the change from baseline in ADPS at week 14, a weekly average of daily patient ratings recorded in an electronic diary. The patient was instructed to rate the pain over the past 24 hours on an NRS (0 = “no pain” to 10 = “worst possible pain”) every morning upon awakening, before taking the study drug.

Secondary efficacy endpoints included responder rate, defined as the percentage of patients with ≥30% and ≥50% reduction from baseline in ADPS; patient-rated pain on the VAS of SF-MPQ; and average daily sleep interference score (ADSIS). The ADSIS was the weekly average of sleep interference as recorded by patients in electronic diaries rated every morning on an NRS of 0 = “pain did not interfere with sleep” to 10 = “pain completely interfered with sleep” over the last 24 hours. Another secondary endpoint was the Patient Global Impression of Change (PGIC), in which patients rated their improvement on a scale from 0 = “very much improved” to 7 = “very much worse” at the end of treatment.

Other secondary endpoints included SF-MPQ (other than VAS), brief pain inventory-short form, medical outcomes study sleep scale, hospital anxiety and depression scale (HADS), 36-item short form health survey (SF-36), and assessment of allodynia and hyperalgesia by the investigator on a 2-point scale (1 = “present,” 2 = “absent”). Allodynia was evaluated by stroking the skin with a brush, and hyperalgesia was evaluated by pressing the skin with a bamboo cooking stick.

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2.3. Safety assessments

Adverse events (AEs) were monitored throughout the study and classified according to the Medical Dictionary for Regulatory Activities, version 17.1. Patients had a total of 11 visits over the 14 weeks, including screening and randomization (week 0). At each visit, clinical laboratory evaluations, physical examinations, and vital signs were monitored. Suicidal behavior and ideation were monitored at each visit using the C-SSRS. In addition, a neurological examination and an electrocardiogram were performed at screening and at the end of treatment or at early termination, and included assessment of muscle strength (0–5 rating; ankle dorsiflexion) and gait/station.

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2.4. Statistical analysis

Sample size was determined to achieve 90% statistical power under the assumption of 0.6 difference vs placebo in change from baseline in ADPS for all mirogabalin groups and a common standard deviation of 1.8 units. The power calculation was based on analysis of variance, and a gatekeeping procedure was applied to control the type I error rate at less than 0.05.

The modified intent-to-treat analysis set, defined as patients who were randomized and received ≥1 dose of the study drug, was used for efficacy analysis. For the primary endpoint (change from baseline in ADPS at week 14 between each group), the multiple imputation method was used to handle missing weekly ADPS data. In the multiple imputation data generation, the Markov Chain Monte Carlo method with treatment group, age, and sex covariates was used to produce a monotone missing data pattern first. The regression with predictive mean matching with the same set of covariates was applied to the monotone missing data. A pattern mixture model with different shift parameters depending on reasons for study discontinuation (AE, lack of efficacy, or other) and was applied to the imputed weekly ADPS data by regression with predictive mean matching to impose penalty on the study discontinuation under a missing not-at-random mechanism.15 To compare change from baseline in ADPS at week 14 between each group receiving ≥ 1 dose of mirogabalin and the placebo group, a mixed-effect model with repeated measures (MMRM) was used for the imputed data sets.18 The MMRM included treatment, week, and treatment-by-week as fixed effects; week as a repeated measure; and baseline ADPS as a covariate. The results from the MMRM analyses were combined using Rubin's rule.22 The following gatekeeping procedure was prespecified to adjust for multiplicity of comparisons between each of mirogabalin groups and placebo4; mirogabalin 20 and 30 mg/day, which have been evaluated and demonstrated efficacy trend in the phase 2 study, were tested against placebo at a significance level of 0.025. If both were statistically significant, mirogabalin 15 mg/day would be tested at a level of 0.05. If neither of them was statistically significant, mirogabalin 15 mg/day would not be tested. If either mirogabalin 20 or 30 mg/day was statistically significant, mirogabalin 15 mg/day would be tested at a level of 0.025.

For secondary endpoints, responder rates (≥30% and ≥50% improvement in ADPS) for mirogabalin groups were compared with the placebo group using a logistic regression model with the treatment group as a factor and baseline ADPS as a covariate. In the analysis, patients who discontinued the study were considered nonresponders and a last observation carried forward (LOCF) approach was used for the imputation for patients who completed the study but did not have week 14 ADPS. The ADSIS was analyzed using MMRM with treatment, week, and treatment-by-week as fixed effects; week as a repeated measure; and baseline ADSIS as a covariate. For the other secondary endpoints, analysis of covariance model with the baseline value as a covariate was used for continuous variables, and a logistic regression model with treatment group as a covariate was applied for categorical variables. Statistical analysis was performed using Statistical Analysis Software (Version 9.3).

All safety data were summarized on the safety analysis set including patients who received 1 dose of study drug. Treatment-emergent AEs (TEAEs) were summarized as a frequency table.

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3. Results

3.1. Patients

A total of 765 patients were randomized to placebo (N = 304) and mirogabalin 15 mg/day (N = 153), 20 mg/day (N = 153), and 30 mg/day (N = 155) (Fig. 2). A total of 763 patients were included in the modified intent-to-treat analysis set population, and 671 (87.7%) patients completed the study. A total of 94 patients (12.3%) discontinued the study; 38 (12.5%) in the placebo group, 16 (10.5%) in the 15 mg/day group, 25 (16.3%) in the 20 mg/day group, and 15 (9.7%) in the 30 mg/day group. The most common reasons for discontinuation were patient withdrawal (25 patients in the placebo group, 7 patients in the 15 mg/day group, 9 patients in the 20 mg/day group, and 10 patients in the 30 mg/day group) and AEs (7 patients in the placebo group, 6 patients in the 15 mg/day group, 12 patients in the 20 mg/day group, and 4 patients in the 30 mg/day group). Randomized patients were mostly male (60.3%) and Japanese (80.0%), with a mean age of 66.5 years (Table 1). Across all treatment groups, the most common site of PHN (45.9%) was the thoracic segment area. The mean ADPS and VAS of the SF-MPQ at baseline were 5.71 and 59.1, respectively.

Figure 2

Figure 2

Table 1

Table 1

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3.2. Efficacy

The ADPS gradually decreased through week 14 in all treatment groups, and all mirogabalin groups had a greater and more rapid decrease of ADPS compared with placebo starting at week 1 (Fig. 3). As the daily dose of mirogabalin increased, there was a greater decrease in least squares (LS) mean ADPS compared with placebo. At week 14, the LS mean change from baseline in ADPS was −1.20, −1.61, −1.68, and −1.97 for the placebo and mirogabalin 15, 20, and 30 mg/day groups, respectively. A statistically significant difference in mean change in ADPS from baseline for all mirogabalin groups vs placebo occurred at week 14; the LS mean vs placebo was −0.41 (95% confidence interval [CI] −0.74 to −0.07, P = 0.0170), −0.47 (95% CI −0.81 to −0.14, P = 0.0058), and −0.77 (95% CI −1.10 to −0.44, P <0.0001) for mirogabalin 15, 20, and 30 mg/day groups, respectively.

Figure 3

Figure 3

The proportion of patients with a ≥30% reduction from baseline in ADPS was 35.0%, 45.4%, 45.1%, and 49.7% for the placebo and mirogabalin 15, 20, and 30 mg/day groups, respectively, with all groups being significantly higher than placebo (Table 2 and Fig. 4). The proportion of patients with a ≥50% reduction from baseline in ADPS was 19.8%, 23.0%, 26.8%, and 29.0% for the placebo and mirogabalin 15, 20, and 30 mg/day groups, respectively, with the 30 mg/day group being significantly higher than placebo (odds ratio 1.63 [95% CI 1.04–2.56], P = 0.0336). The LS mean change from baseline to week 14 in VAS of the SF-MPQ and the ADSIS was significantly greater in all mirogabalin groups compared with placebo (Table 2).

Table 2

Table 2

Figure 4

Figure 4

Significantly more patients treated with mirogabalin 15 mg/day vs placebo reported a PGIC of “much improved or better (score ≤2)” at week 14 (36.2% vs 26.4%, P = 0.0318), and significantly more patients treated with mirogabalin 20 and 30 mg/day vs placebo reported a PGIC score of “minimally improved or better (score ≤3)” (69.3% and 69.0% vs 54.5%, respectively; P = 0.0025 and 0.0028, respectively) (Fig. 5).

Figure 5

Figure 5

At week 14, the changes from baseline in the SF-MPQ (excluding VAS) showed greater improvement in all mirogabalin groups vs placebo. For the SF-MPQ subscales (sensory score, affective score, total score, and present pain intensity), the LS mean differences in change from baseline at week 14 were significantly greater in all mirogabalin groups vs placebo.

The changes from baseline in the brief pain inventory-short form subscales at week 14 showed greater improvement in all mirogabalin groups vs placebo. The LS mean differences in change from baseline for worst pain, average pain, and pain right now were statistically significant for all mirogabalin groups vs placebo, with the greatest difference seen in the mirogabalin 30 mg/day group. The LS mean difference in change from baseline for impact on daily function vs placebo was statistically significant in the mirogabalin 20 mg/day and 30 mg/day group vs placebo.

At week 14, the LS mean differences in change from baseline vs placebo for the medical outcomes study subscales of sleep disturbance and sleep somnolence increased improvement as the daily dose of mirogabalin increased.

The changes from baseline for the HADS subscales of depression and anxiety at week 14 were greater in all mirogabalin groups vs placebo. The LS mean differences in change from baseline were statistically significant vs placebo in all mirogabalin groups for the anxiety subscale and in the 15 mg/day group for the depression subscale.

The LS mean changes from baseline at week 14 for the SF-36 subscales of physical functioning, role-physical, bodily pain, general perception of health, vitality, social functioning, role-emotional, and mental health were greater in all mirogabalin groups vs placebo.

No notable differences were found in the percentage of patients with allodynia and those with hyperalgesia at week 14 between the treatment groups.

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3.3. Safety and tolerability

The most common TEAEs (≥5%) are summarized in Table 3. The most common TEAEs were somnolence, dizziness, weight increase, and edema; all occurred more frequently in all mirogabalin groups than in the placebo group. The incidence of somnolence, dizziness, and edema increased as the daily dose of mirogabalin increased. Overall, the majority of the most common TEAEs were mild or moderate, and all resolved without treatment. Forty-eight patients (6.3%) had ≥ 1 TEAE leading to treatment discontinuation; 12 (4.0%) in the placebo group, 8 (5.3%) in the 15 mg/day group, 16 (10.5%) in the 20 mg/day group, and 12 (7.7%) in the 30 mg/day group. Fifteen patients, 5 in the 15 mg/day group, 2 in the 20 mg/day group, 3 in the 30 mg/day group, and 5 in the placebo group, had a serious TEAE. No specific serious TEAEs were reported more frequently in any treatment group, and overall, the incidence of serious TEAEs was low. Three patients, 2 in the mirogabalin 30 mg/day group and 1 in the placebo group, had a severe TEAE of increased blood creatine phosphokinase; all resolved without treatment. Other severe TEAEs included Meniere disease, acute myocardial infarction, and radius fracture in the placebo group; pneumonia, rib fracture, and femur fracture in the 15 mg/day group; erectile dysfunction, fracture, and upper-limb fracture in the 20 mg/day group; and memory impairment, altered state of consciousness, cerumen impaction, and electrocardiogram change in the 30 mg/day group.

Table 3

Table 3

No notable changes were observed in electrocardiograms, vital signs, neurological examination, hematology, blood chemistry, or urinalysis. No patients answered “yes” to any question in C-SSRS regarding suicidal behavior and ideation.

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4. Discussion

The findings reported here demonstrate that mirogabalin is effective and well tolerated for the management of PHN in Asian patients. In a large UK database of primary care records, approximately 5.8% of patients with herpes zoster developed PHN; of Japanese adults aged 50 years and older with herpes zoster, approximately 20% developed PHN.13,23 There are 2 possible reasons for this difference. The first reason is the difference in the age of study patients. The data from the study in Japan include patients older than 50 years, whereas the data from the UK study include patients younger than 50 years. The other possible reason for the epidemiologic difference is the late implementation of the herpes zoster vaccine in Japan. The herpes zoster vaccine for persons older than 50 years became available in Japan in 2016, compared with 2013 in the United Kingdom.

Mirogabalin doses of 15 to 30 mg/day were well tolerated. All mirogabalin groups demonstrated a statistically significant improvement in ADPS vs placebo, and the improvements were greater as the daily dose of mirogabalin was increased, but the difference between the daily doses were not statistically significant. The Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials II and IV consensus recommends that ≥30% reduction in pain intensity from baseline can be considered a clinically important difference when measured on an NRS in a chronic pain clinical trial.8,10 In this study, the NRS reduction rate from baseline of placebo was approximately 20%; mirogabalin 15 and 20 mg/day had a reduction rate from baseline of approximately 30%; and mirogabalin 30 mg/day had a reduction rate of approximately 35% in this study. A total of 45% to 50% of patients achieved a ≥30% reduction in ADPS across all mirogabalin treatment groups. Sleep dysfunction is a common comorbidity in patients with PHN6 and is associated with worse pain outcomes. All doses of mirogabalin significantly improved the ADSIS.

In this study, the baseline total ADPS was 5.71, which is lower than previous clinical trials of gabapentinoids.7,21 We excluded patients who reported extreme pain as a method to improve the assay sensitivity,9 particularly, patients with a pain scale ≥90 mm on VAS of SF-MPQ at screening and randomization, or a daily pain score ≥9 during the observation period. This exclusion possibly contributed to the lower baseline total ADPS, which in turn may correlate with the lower efficacy of mirogabalin.

Patients with PHN also often have difficulty with activities of daily living and a decreased QoL.6,14 Mirogabalin demonstrated statistically significant improvements in the ADPS, ADSIS, and PGIC scores vs placebo, indicating a possible improvement in activities of daily living and QoL. The mean ADPS for mirogabalin at week 14 decreased compared with baseline in all treatment groups vs placebo, and the results of the secondary analyses were consistent with the efficacy seen in the primary analyses.

For the handling of missing data for some of the secondary endpoints, the LOCF approach, which is no longer generally appropriate for clinical trials of chronic pain disease, was applied. We agree that a more appropriate approach should have been applied; however, if a more appropriate approach had been applied, we believe that the impact on the results would be limited because of the small number of discontinued subjects for each treatment group and small number of differences in discontinued subjects between treatment groups in our study.

The most common AEs were somnolence, dizziness, and weight increase, which were expected based on the mechanism of action of mirogabalin, and a similar result was reported in the phase 2 DPNP study of 5 weeks in the United States.26 In the phase 2 study by Vinik et al.,26 mirogabalin 30 mg/day had a higher incidence of somnolence (12.3% vs 8.0%) and dizziness (15.8% vs 6.0%) vs pregabalin 300 mg/day. To reduce AEs, this study adopted more gradual titration of mirogabalin compared with the US phase 2 study. When indirectly comparing the current phase 3 TEAEs with the treatment-related AEs reported for pregabalin 300 mg/day in the phase 3 study of Japanese patients with PHN, the incidence of somnolence was similar with mirogabalin 30 mg/day vs pregabalin 300 mg/day (23.9% vs 24.7%), but the incidence of dizziness and weight increase were lower (15.5% vs 30.3%, 5.2% vs 16.9%, respectively).20 Peripheral edema, a common AE in the pivotal studies of pregabalin for DPNP and PHN, also occurred at lower incidence in mirogabalin 30 mg/day group compared with pregabalin 300 mg/day (2.6% vs 12.4%). This result supports the use of mirogabalin as an alternative therapeutic option for PHN.

Mirogabalin can be flexibly selected depending on individual patient response and tolerability in a dose range from 15 to 30 mg/day. In this study, there was a titration period for each mirogabalin group; mirogabalin 5 or 10 mg/day was administered for the first week, then increased in a step-wise manner. The step-wise increase in dosing for α2δ ligands helps increase patient tolerance and decrease AEs; the Japanese Society of Pain Clinicians recommend starting pregabalin at initial doses of 25 to 150 mg/day and increasing by 25 to 150 mg/day every 3 to 7 days.24

For the ideal dosing frequency, because elimination half-life of mirogabalin is estimated to be about 3 hours, plasma concentration of mirogabalin reaches baseline approximately 12 hours after administration. Thus, twice-daily dosing is the reasonable dosing frequency.

In addition, the incidence of somnolence and dizziness (common AEs of gabapentinoids) are correlated with the maximum plasma concentration (Cmax) with internal assessment; this leads us to believe that the incidence of somnolence and dizziness will be lower when administered twice daily vs once daily (data will be published later). Regarding more frequent doses, such as 3 times daily, we did not try this regimen from the viewpoint of drug compliance and patient convenience.

This study has a few limitations. First, only Asian patients were enrolled in the study; studies have shown there may be difference in pain intensity between ethnic groups.1 However, the phase 2 DPNP study was conducted in the United States, with 72.3% of patients being white and 24.1% of patients being black, and had favorable results for mirogabalin, which suggest mirogabalin might be efficacious in patients of different ethnicities.26 Second, all patients met the inclusion criteria of creatine clearance of ≥60 mL/minute as determined by the Cockcroft–Gault equation, so efficacy in patients with PHN and renal impairment cannot be determined from this analysis. Further studies are needed to determine the appropriate doses for these patients.

An additional limitation of this study is that the patients who received the 15-mg/day dose only received the medication at night. This could lead to decreased AEs during the day, including decreased daytime somnolence. The decrease in daytime AEs for the 15 mg/day group and also for the group that received placebo could result in potential unintended unblinding for the investigators.

The abuse liability of mirogabalin was not evaluated in this study; 2 randomized, double-blind, placebo-controlled studies using either pregabalin or diazepam as positive controls were undertaken; and the results will be reported in a separate publication.

In summary, mirogabalin has demonstrated a well-balanced profile of efficacy and safety and may provide an alternative therapeutic option for the treatment of PHN.

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Conflict of interest statement

E. Murayama, M. Sugihara, N. Matsui, S. Ohwada, and Y. Kakehi are employees of Daiichi Sankyo Co, Ltd. J. Kato reports personal fees from Daiichi Sankyo Co, Ltd, during the conduct of the study; and personal fees from Pfizer Japan Inc; Eisai Co, Ltd; and Mochida Pharmaceutical Co, Ltd.

Parts of these study results were presented at the 52nd Annual Meeting of the Japan Society of Pain Clinicians, July 19–21, 2018, Tokyo, Japan.

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Acknowledgments

Writing and editorial assistance, under consideration by Daiichi Sankyo authors, was provided by Jennifer Meyering, RN, MS, of AlphaBioCom, LLC, King of Prussia, PA, and supported by Daiichi Sankyo, Co., Ltd., Basking Ridge, NJ. This study was funded by Daiichi Sankyo Co., Ltd. and Daiichi Sankyo, Inc.

The authors thank the following investigators for their assistance in the clinical trials: Toshimitsu Kawashima (Abashiri Dermatology Clinic); Mitsuko Mimura (NTT East Sapporo Hospital); Ichiro Tsukinaga (KKR Sapporo Medical Center); Fumio Tanioka (Sapporo Asabu Clinic); Hiroshi Sugawara (Kokubu Dermatology Clinic); Yuko Morita (Maruyama Lila Clinic); Hiroto Fudeta, Hideyuki Toukairin (Sendai City Hospital); Hisashi Date (Sendai Pain Clinic Center); Akiko Izuha (Japanese Red Cross Fukushima Hospital); Hiroaki Maru (Fujita General Hospital); Keiichi Kan (Southern TOHOKU Research Institute for Neuroscience, Southern TOHOKU General Hospital); Manabu Otsuki (Otsuki Sleep Clinic); Naomitsu Okubo (Mito Saiseikai General Hospital); Shigeki Yamaguchi (Dokkyo Medical University Hospital); Akira Tanaka (Gunma Pain Clinic Hospital); Hiroaki Kimura (Kimura Pain Clinic); Kou Miyashita (Takasaki Pain Clinic); Tetsujiro Suzuki (Kumagaya General Hospital); Hiroshi Kobayashi (Kobayashi Clinic); Kodai Kinoshita (Kinoshita Clinic); Yuzo Mouri (Nagomi Pain Clinic); Taketo Hotta (Hotta Dermatology Clinic); Kazuhiro Inafuku (Kimitsu Chuo Hospital); Yoichiro Kamiyama (Juntendo University Urayasu Hospital); Yasuyo Nakashima (Kuriyama Central Hospital); Chol Kim (Nippon Medical School Chiba Hokusoh Hospital); Ryuichi Suzuki (Suzuki Dermatology and Internal Medicine Clinic); Rokusuke Koshida (Koshidaiin Internal Medicine and Surgery Pain Clinic); Takahiro Suzuki (Nihon University Itabashi Hospital); Atsuyuki Igarashi, Yoichiro Abe (NTT Medical Center Tokyo); Masahide Kubo, Yuriko Kishi, Naoko Kanda (JCHO Tokyo Shinjuku Medical Center); Kiyoshige Ohseto (Tokyo Medical University Hospital); Kazuhiro Toriumi (Toriumi Pain Clinic); Masako Iseki (Juntendo University Hospital); Masahiko Sumitani (The University of Tokyo Hospital); Hideki Mukai, Hidetsugu Fukuda (Toho University Ohashi Medical Center); Yoshihiro Kuwano (Showa General Hospital); Motoi Sasuga (Tokyo Metropolitan Tama Medical Center); Shohei Futaki (Futaki Skin Care Clinic); Yasuhiro Maehara (National Center for Global Health and Medicine); Hitoshi Mera (Ebara Hospital); Kiyoshi Murayama (Nihonbashi Murayama Clinic); Kenji Shida (Showa University Hospital East Branch); Seiyu Higa (Mitaka Pain Clinic); Akiko Miyazawa (Miyazawa Clinic); Masahiro Shiotani (Shiotani Pain Clinic); Yoshikazu Naganuma (Naganuma Pain Clinic); Mariko Kawate (Nishiogi Pain Clinic); Yasuo Fukuuchi (Fukuuchi Pain Clinic); Sumio Oura (Soken Dermatology Clinic); Taizou Hamaguchi (Hamaguchi Skin Clinic); Hideki Ito (Tachikawa Dermatology Clinic); Jun Hasegawa (Sakurashinmachi Pain Clinic); Hanako Ohmatsu (National Hospital Organization Sagamihara National Hospital); Akifumi Kanai (Kitasato University Hospital); Naosuke Sugai (Shonan Fujisawa Tokushukai Hospital); Nobuko Maeda, Yuhi Yamamoto, Tomohiko Tanegashima (Hiratsuka Kyosai Hospital); Hideki Toyokawa (Nishitsuruma Medical Clinic); Shunichi Miyakawa (Kawasaki Municipal Hospital); Tetsuya Yokota (Kanto Rosai Hospital); Junya Irimajiri (Shonan Kamakura General Hospital); Norimitsu Saito (Yokohama Rosai Hospital); Tokuya Omi (Queen's Square Medical Center); Yuko Nomura (Nomura Dermatology Clinic); Toshiya Asai (Asai Dermatology Clinic); Etsuro Hajiri (Hajiri Pain Clinic); Yumito Suzuki (Suzuki Pain Clinic); Ken Watanabe (Yokohama City Minato Red Cross Hospital); Shigeyuki Tai (Tai Clinic); Rika Hayashi (Yokohama Bashamichi Skin & Pain Clinic); Shunichi Nitta (Ishikawa Prefectural Central Hospital); Fumiaki Abe (Yamanashi Prefectural Central Hospital); Fuyuko Arakura (National Hospital Organization Matsumoto Medical Center Matsumoto Hospital); Masao Fukuzawa (Ina Central Hospital); Shoko Urano (JA Shizuoka Kohseiren Enshu Hospital); Akihito Mizutani (Mizutani Pain Clinic); Manabu Inuzuka (Chutoen General Medical Center); Hironaka Tsunobuchi (Fujita Health University Banbuntane Hotokukai Hospital); Masanari Kodera (JCHO Chukyo Hospital); Hideaki Kato (Yachiyo Hospital); Tetsuro Onuma (Narita Memorial Hospital); Daisuke Watanabe (Aichi Medical University Hospital); Tomomasa Kimura (Kimura Clinic); Koji Habe (Mie University Hospital); Sei Fukui (Shiga University of Medical Science Hospital); Ken Sasaki (Sasaki Pain Clinic); Atsuko Kato (Osaka Kaisei Hospital); Mari Higashiyama (Nissay Hospital); Yoichi Matsuda (Osaka University Hospital); Ryuta Ikegami (JCHO Osaka Hospital); Taeko Yoshikawa (Hokusetsu General Hospital); Masahiro Morimoto (Kindai University Hospital); Mami Morimoto (Yusaido Morimoto Clinic); Akihiro Kume (Dermatology and Ophthalmology Kume Clinic); Yumiko Takao (Kobe University Hospital); Ichiro Kurokawa (Meiwa Hospital); Lynn Maeda (Nishinomiya Municipal Central Hospital); Harumasa Nakamura (Nakamura Clinic); Kieun Park (Paku Pain Clinic); Fujio Yanamoto (Ashiya Yanamoto Pain Clinic); Hiroshi Iranami (Japanese Red Cross Wakayama Medical Center); Wook-kang Huh (Dr. Huh's Dermatology Clinic); Katsuyuki Moriwaki (National Hospital Organization Kure Medical Center and Chugoku Cancer Center); Itsuo Nakagawa (Chugoku Rosai Hospital); Hirofumi Morikawa (Hiroshima General Hospital); Hidenori Harada (Yamaguchi University Hospital); Haruhiko Manabe (Kitakyushu Municipal Medical Center); Bungo Ohyama (Kurume University Hospital); Reiji Kaieda (Fukuoka Tokushukai Medical Center); Shu Iwanaga (Yagi Hospital); Masakazu Nagata (Nagata Dermatology Clinic); Shunichi Ariyoshi (Ariyoshi Clinic); Keiji Okubo (Okubo Skin Care and Clinic); Keizo Matsuo (Matsuo Clinic); Shinichi Koba (Saga-ken Medical Centre Koseikan); Ryo Katsuki (National Hospital Organization Ureshino Medical Center); Tetsuya Sakai, Itsuko Shibata (Nagasaki University Hospital); Takahiro Tamura (Tamura Dermatology Clinic); Kentaro Okuda (Oita University Hospital); Toru Fujigaki (Fujigaki Clinic); Nozomu Toyama (Toyama Dermatology Clinic); Takeshi Uno, Shingo Tateyama (Junwakai Memorial Hospital); Takaki Hashiguchi (Hashiguchi Dermatology); Sang Chul Lee, Jee Youn Moon (Seoul National University Hospital); Hue Jung Park (The Catholic University of Korea, Seoul St. Mary's Hospital); Pyung-Bok Lee (Seoul National University Bundang Hospital); Duck Mi Yoon (Severance Hospital, Yonsei University); Jung-Ju Choi (Gachon University Gil Medical Center); Myung Ha Yoon (Chonnam National University Hospital); Do Wan Kim (Ajou University Hospital); Gill Hoi Koo, Hwa-Yong Shin (Chung-Ang University Hospital); DaeHyun Jo (The Catholic University of Korea, Daejeon St. Mary’s Hospital); Woo Seog Sim (Samsung Medical Center); YoungHoon Jeon (Kyungpook National University Hospital); Young Deog Cha (Inha University Hospital); Sang Sik Choi (Korea University Guro Hospital); Won Hyung Lee (Chungnam National University Hospital); Jeong Hun Suh (Asan Medical Center); Hye-Won Lee, Ji-Yong Park (Korea University Anam Hospital); Hahck Soo Park, Won-joong Kim (Ewha Womans University Mokdong Hospital); SangGon Lee (Daegu Fatima Hospital); Jae Hun Kim (Konkuk University Medical Centr); Myoung Jin Ko, Sang Eun Lee (Inje University Haeundae Paik Hospital); Yeon-Dong Kim (Wonkwang University Hospital); SunOk Song (Yeungnam University Hospital); Kyoung-Hoon Yim, Chanjin Park (Chungbuk National University Hospital); Joon Ho Lee (Soon Chun Hyang University Hospital Bucheon); JiHee Hong (Keimyung University Dongsan Hospital); Shuu-Jiun Wang (Taipei Veterans General Hospital); Wei-Zen Sun (National Taiwan University Hospital); Yi-Jer Hsieh (Changhua Christian Hospital); Chih-Cheng Chien (Cathay General Hospital); Long-Sun Ro (Chang Gung Memorial Hospital, Linkou); Chia-Shiang Lin (Mackay Memorial Hospital); Jia-Ying Sung (Taipei Municipal Wanfang Hospital); Ming-Hong Chang (Taichung Veterans General Hospital); Kuang-I Cheng (Kaohsiung Medical University Chung-Ho Memorial Hospital); Yuh-Cherng Guo (China Medical University Hospital); Kao-Chang Lin (Chi Mei Medical Center); Jiunn-Tay Lee (Tri-Service General Hospital); Yam-Ting Kwok (Far Eastern Memorial Hospital); Cheng Yin Tan (University Malaya Medical Centre); Kim Swan Ng (Hospital Selayang); Kavita Bhojwani (Hospital Raja Permaisuri Bainun); Kiung Sze Ting, Lim Ern Ming (Hospital Kuala Lumpur); Irene Looi (Hospital Seberang Jaya); Kanoksri Samintharapanya (Lampang Hospital); Sombat Muengtaweepongsa (Thammasat University Hospital); Tasanee Tantirittisak (Presat Neurological Institute); Arkhom Arayawichanont (Sunprasitthiprasong Hospital); Charoen Choonhakarn (Srinagarind Hospital); Kian Hian Tan (Singapore General Hospital- Parent); Jiun Yit Pan (National Skin Centre); Derrick Aw (National University Hospital); and Kok Yuen Ho (Raffles Hospital).

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Keywords:

Pain; Postherpetic neuralgia; Pain medicine; α2δ-ligand

© 2019 International Association for the Study of Pain