ARISE: A Phase 3 randomized trial of erenumab for episodic migraine

Abstract

Background

Calcitonin gene-related peptide plays an important role in migraine pathophysiology. Erenumab, a human monoclonal antibody that inhibits the calcitonin gene-related peptide receptor, is being evaluated for migraine prevention.

Methods

In this randomized, double-blind, placebo-controlled, phase 3 study, 577 adults with episodic migraine were randomized to placebo or 70 mg erenumab; 570 patients were included in efficacy analyses. Primary endpoint was change in monthly migraine days. Secondary endpoints were ≥50% reduction in monthly migraine days, change in acute migraine-specific medication treatment days, and ≥5-point reduction in Physical Impairment and Impact on Everyday Activities domain scores measured by the Migraine Physical Function Impact Diary. All endpoints assessed change from baseline at month 3.

Results

Patients receiving erenumab experienced −2.9 days change in monthly migraine days, compared with −1.8 days for placebo, least-squares mean (95% CI) treatment difference of −1.0 (−1.6, −0.5) (p < 0.001). A ≥ 50% reduction in monthly migraine days was achieved by 39.7% (erenumab) and 29.5% (placebo) of patients (OR:1.59 (95% CI: 1.12, 2.27) (p = 0.010). Migraine-specific medication treatment days were reduced by −1.2 (erenumab) and −0.6 (placebo) days, a treatment difference of −0.6 (−1.0, −0.2) (p = 0.002). The ≥5-point reduction rates in Migraine Physical Function Impact Diary – Physical Impairment were 33.0% and 27.1% (OR:1.33 (0.92, 1.90) (p = 0.13) and in Migraine Physical Function Impact Diary – Everyday Activities were 40.4% and 35.8% (OR:1.22 (0.87, 1.71) (p = 0.26). Safety and adverse event profiles of erenumab were similar to placebo. Most frequent adverse events were upper respiratory tract infection, injection site pain, and nasopharyngitis.

Conclusions

As a preventive treatment of episodic migraine, erenumab at a dosage of 70 mg monthly significantly reduced migraine frequency and acute migraine-specific medication use. (Funded by Amgen).

Trial registration

ClinicalTrials.gov, NCT02483585.

Keywords

Erenumab migraine safety efficacy calcitonin gene-related peptide

Introduction

Despite the availability of several oral preventive therapies for migraine, patients often discontinue treatment due to lack of efficacy or poor tolerability (1–5). Moreover, most of the drugs used in preventive treatment of migraine were initially designed for other purposes, reflecting the need for newer migraine-specific therapeutic agents. Calcitonin gene-related peptide (CGRP) is a neuropeptide implicated in migraine pathophysiology (6–10). Ample clinical evidence shows that CGRP and the CGRP receptor are suitable targets for the acute and preventive treatment of migraine (6,11–15). Erenumab (AMG 334) is a fully human monoclonal antibody that targets and blocks the canonical CGRP receptor (16,17).

ARISE (A Phase 3, RandomIzed, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of AMG 334 in Migraine Prevention), a large multi-national, placebo-controlled phase 3 study of erenumab 70 mg in episodic migraine (EM) was conducted to confirm the efficacy and safety results of a phase 2 dose-ranging study that established 70 mg as the minimally effective dose (14). Here, we report the primary results for the 12-week placebo-controlled, double-blind treatment phase of ARISE.

Methods

Trial population

Adults (18 to 65 years old) with a history of EM (≥4 to <15 migraine days per month and < 15 headache days per month) (18) with or without aura for at least 12 months prior to the study were eligible. Patients older than 50 years of age at migraine onset, with a history of hemiplegic migraine or cluster headache, were excluded. Patients with prior treatment failures (based on efficacy or tolerability) were allowed in the study except when there was no therapeutic response to more than two classes of migraine prevention treatments (defined as an adequate trial of at least 6 weeks at the recommended dose without any benefit in terms of frequency, duration, or severity of the attacks, according to the investigator’s opinion). In the initial protocol, medications with possible migraine preventive effects were prohibited, though patients who had received preventive drugs could participate following washout for at least 2 months prior to baseline or 4 months for botulinum toxin (Supplementary Appendix). Subsequently, a protocol amendment allowed for concomitant use of only one migraine preventive medication if the dose was stable within two months before the baseline phase and was to remain stable throughout the study. Patients with medical conditions that might prevent study completion or interfere with interpretation of results were excluded (Supplementary Appendix). Women of child bearing potential had to use an effective contraceptive method.

Trial oversight

Institutional review boards at each center approved the study protocol. All patients provided written informed consent. Sites maintained compliance with the Health Insurance Portability and Accountability Act or relevant regional regulations. The study was conducted in accordance with the International Conference on Harmonisation Tripartite Guideline on Good Clinical Practice. An independent data monitoring committee reviewed and made recommendations regarding the safety of study participants throughout the double-blind treatment phase and until treatment assignment information was available to the study team for the primary analysis. Site investigators collected the data and Amgen conducted the data analyses according to a pre-specified statistical analysis plan. All authors interpreted the data and collaborated in manuscript preparation with support from a professional medical writer, funded by Amgen. All authors made the decision to submit the manuscript and attested to the veracity and completeness of data and analyses for their respective studies and the fidelity of this report to the study protocol. Amgen funded the study. A copy of the protocol is available at https://www.clinicaltrialsregister.eu EudraCT number 2014-004463-20.

Trial design

ARISE was a multicenter, randomized, double-blind, placebo-controlled, parallel-group, phase 3 trial conducted at 69 sites across North America and Europe (including Russia) from July 2015 (first patient randomized) to July 2016 (data cutoff date for primary analysis or primary completion date). The study was conducted in headache centers, neurology clinics, and clinical research sites. Eligible patients were recruited into the study by participating sites, where subjects were regularly followed for headache, and via advertisement.

The study comprised a screening phase (up to 3 weeks), a 4-week baseline phase, a 12-week double-blind treatment phase, and a 28-week open-label treatment phase. A safety follow-up visit was completed 12 weeks after last dose of investigational product. Primary results from the double-blind treatment phase of the study are reported here. Results from the open-label treatment and safety follow-up phases have not been completed and will be reported separately.

Patients were randomized 1:1 to erenumab 70 mg or placebo (monthly subcutaneous injection). Randomization was based on a computer-generated schedule created by the sponsor before study initiation and was centrally executed using an interactive response system. Eligibility was evaluated and confirmed by the principal investigator. Randomization was stratified by region (North America vs. other) and preventive migraine medication status ((a) current migraine preventive treatment; (b) prior migraine preventive treatment only; (c) no prior or current migraine preventive treatments). Patients, site personnel, and study sponsor personnel were blinded to treatment group assignment during the double-blind treatment phase. Erenumab and placebo were packaged identically in size and color to maintain the blind. At week 12, all patients continuing into the open-label treatment phase were to receive open-label 70 mg erenumab.

Assessments and safety evaluations

We conducted efficacy assessments throughout the baseline and double-blind phase of the study, with key assessments at week 12 (during the last month of the double-blind treatment phase). Patients used an electronic headache diary every day throughout the baseline phase and double-blind treatment phase to report information about their migraine and non-migraine headaches and acute headache medication use, including date and time of onset and resolution of headache, headache pain severity and pain features, associated symptoms, use of acute headache medication, and patient-reported outcomes (PRO) via the Migraine Physical Function Impact Diary (MPFID) (19). Additional PRO measures (including Headache Impact Test [HIT-6^T] (20,21), Modified Migraine Disability Assessment [mMIDAS; measured as 4-week recall period vs. 3-month recall of standard MIDAS] (22), and Migraine-Specific Quality-of-Life Questionnaire [MSQ] (23,24)) were collected at pre-specified assessment times. We evaluated safety by monitoring adverse events (AEs) (Medical Dictionary for Regulatory Activities v19.0) (25), serious AEs (26), laboratory assessments, vital signs, electrocardiograms, and anti-erenumab antibodies.

Objectives and endpoints

The primary objective was to confirm the effect of erenumab compared to placebo for the primary endpoint of change from baseline in monthly migraine days (MMD) in the last month (month 3) of the double-blind treatment phase. A migraine day was defined as any calendar day recorded in the electronic headache diary on which the patient had an onset, continuation, or recurrence of a qualified migraine, defined as a migraine (with or without aura) lasting ≥ 30 minutes and presenting with at least two pain features (unilateral, throbbing, moderate to severe, or aggravated by physical activity) and/or at least one associated non-pain feature (nausea and/or vomiting, or both photophobia and phonophobia). Use of acute migraine-specific medication (triptans or ergotamine derivatives) on a calendar day was counted as a migraine day, irrespective of the duration of the migraine. Prespecified secondary endpoints included achievement of ≥50% reduction from baseline in MMD, change from baseline in monthly acute migraine-specific medication treatment days (MSMD), achievement of at least a 5-point reduction in monthly average Physical Impairment domain score as measured by the Migraine Physical Function Impact Diary (MPFID-PI), and achievement of at least a 5-point reduction in monthly average Impact on Everyday Activities (MPFID-EA) domain score. Exploratory PRO endpoints included change from baseline in HIT-6, modified (monthly) MIDAS, MSQ, and MPFID. All endpoints were assessed over the last month (month 3) of the double-blind treatment phase.

Statistical analysis

Sample size was based on the primary endpoint of change from baseline in monthly migraine days in the last month of the double-blind treatment phase. Assuming a treatment effect compared to placebo of −1.12 for the erenumab 70 mg group and a common standard deviation of 3.78, the planned sample size of 270 subjects per group would provide 90% power using a two-sample t-test with a 2-sided significance level of 0.05. A 10% dropout rate was assumed. The assumed treatment effect of erenumab 70 mg was based on the mean difference compared to placebo and common standard deviation observed in the phase 2 trial (12).

Primary analyses were conducted after all patients completed the 12-week visit or prematurely terminated the study before the 12-week visit. The statistical significance levels of the primary and secondary endpoints were determined after multiplicity adjustment using a pre-specified hierarchical gate-keeping procedure and Hochberg-based testing procedures to maintain the 2-sided study-wise type I error rate at α = 0.05 (Supplementary Appendix). p values that were considered statistically significant are described as such in text and identified in tables. p values for exploratory endpoints were nominal and were not adjusted for multiple comparisons. Continuous variables were analyzed using a linear mixed effects model including treatment group, baseline value, stratification factors (region and preventive migraine medication status), scheduled visit, and the interaction of treatment group with scheduled visit, without any imputation for missing data. Dichotomous variables were analyzed using a stratified Cochran-Mantel-Haenszel test and using non-responder imputation, in which missing data was assumed to be non-response. The full analysis set included all patients who were randomized in the study. The efficacy analysis set included all patients who received at least one dose of randomized treatment and had at least one change from baseline measurement for MMD during the double-blind treatment phase, analyzed according to randomized treatment. The safety-analysis set, which included all randomized patients who received one or more doses of investigational product, was used to analyze adverse event incidence rates according to randomized treatment group unless a patient received an incorrect dose throughout the entire double-blind treatment phase.

Results

Patients

Demographics and baseline disease characteristics were balanced between treatment groups (Table 1). Of 887 patients screened, 577 patients were randomized, of whom 546 (95%) completed week 12 (Supplementary Table S1 and Supplementary Figure S2). Mean (SD) age of the patients was 42 (11) years and 85.3% of patients were female with a mean (SD) duration of disease of 21 (12) years (Table 1). Of 266 (46.1%) patients with prior preventive treatment use, the vast majority (n = 232, 87.2%) failed one or more medications due to lack of efficacy or poor tolerability (Table 1). During the baseline period, MMD was 8.3 (2.6) days and MSMD was 3.6 (3.6) days, with 61.0% of patients using acute migraine-specific medication during the baseline phase (Table 1).

Table 1.

Demographics and baseline characteristics of the patients*.

	Placebo n = 291	Erenumab 70 mg n = 286
Age, years	42 ± 12	42 ± 11
Female sex, no (%)	247 (84.9)	245 (85.7)
White race, no (%)†	259 (89.0)	259 (90.6)
Weight, kg	76 ± 19	77 ± 19
Body-mass index‡	27.4 ± 6.1	27.4 ± 6.3
Age at onset of migraine, years	22 ± 11	21 ± 10
Duration of disease, years	20 ± 12	22 ± 13
History of aura (yes), no (%)	144 (49.5)	146 (51.0)
Prior prophylactic therapy (yes), no (%)
Naïve	150 (51.5)	144 (50.3)
Prior use only	125 (43.0)	123 (43.0)
Current use	16 (5.5)	19 (6.6)
Acute headache medication use, no (%)	283 (97.3)	280 (97.9)
Migraine-specific	174 (59.8)	178 (62.2)
Non-migraine-specific	236 (81.1)	224 (78.3)
History of any prior preventive treatment use, no (%)	132 (45.4)	134 (46.9)
History of any prior preventive treatment failure§	115 (87.1)	117 (87.3)
Baseline period
Monthly migraine days	8.4 ± 2.6	8.1 ± 2.7
Monthly migraine attacks	5.2 ± 1.5	5.1 ± 1.5
Monthly headache days	9.3 ± 2.7	9.1 ± 2.7
Monthly acute migraine- specific medication days	3.4 ± 3.6	3.7 ± 3.6
Monthly MPFID impact on everyday activities score¶	13.2 ± 8.9	12.6 ± 8.6
Monthly MPFID physical impairment score¶	11.5 ± 9.2	10.8 ± 9.1

Plus-minus values are means ± standard deviation.

†

Race was self-reported.

‡

The body-mass index is the weight in kilograms divided by the square of the height in meters.

Failure due to lack of efficacy or poor tolerability.

MPFID scores range from 0–100, with higher scores indicating greater impact.

MPFID: Migraine Physical Function Impact Diary.

Primary efficacy endpoint

Erenumab was superior to placebo with respect to the primary endpoint (Table 2; p < 0.001) (Figure 1). At week 12, those receiving erenumab experienced a least-squares mean −2.9-day change from baseline in MMD, compared to a −1.8-day change for placebo, representing a difference from placebo in least squares mean (95% confidence interval) of −1.0 (−1.6, −0.5) days (p < 0.001).

Table 2.

Primary and secondary endpoints at week 12*.

	Placebo n = 288	Erenumab 70 mg n = 282	p value†
Monthly migraine days
Change from baseline	−1.8 ± 0.2	−2.9 ± 0.2
Difference from placebo (95% CI)		−1.0 (−1.6, −0.5)	<0.001‡
≥50% reduction from baseline, no (%)	85 (29.5)	112 (39.7)
Odds ratio (95% CI)‡		1.59 (1.12, 2.27)	0.010‡
Monthly acute migraine-specific medication days
Change from baseline	−0.6 ± 0.1	−1.2 ± 0.1
Difference from placebo (95% CI)		−0.6 (−1.0, −0.2)	0.002‡
MPFID everyday activities
≥5-point reduction, no (%)	103 (35.8)	114 (40.4)
Odds ratio (95% CI)§		1.22 (0.87, 1.71)	0.26
MPFID physical impact
≥5-point reduction, no. (%)	78 (27.1)	93 (33.0)
Odds ratio (95% CI)§		1.33 (0.92, 1.90)	0.13

Data are least-squares means ± SE unless otherwise indicated. N values are the number of patients who were randomized and had at least one change from baseline measurement in monthly migraine day during the double-blind phase.

†

p values for pairwise comparison are unadjusted. Primary and secondary endpoints were tested with a hierarchical testing procedure with a prespecified order.

‡

Primary and first tier secondary endpoints were significant after multiplicity adjustment.

The adjusted odds ratios and p values are obtained from a Cochran-Mantel-Haenszel (CMH) test after the missing data are imputed as non-response, stratified by stratification factors region and prophylactic migraine medication status.

CI: confidence interval; MPFID: Migraine Physical Function Impact Diary.

Figure 1.

Efficacy over time. Least-squares mean changes from baseline in monthly migraine days (MMD) (Panel a) and monthly acute migraine-specific medication treatment days (MSMD) (Panel b) among patients with episodic migraine who were assigned to receive erenumab 70 mg or placebo every month. The error bars represent 95% confidence intervals (95% CI). Figure based on the efficacy analysis set. *p < 0.05, ^†p < 0.005, ^‡p < 0.001 for erenumab vs. placebo (statistical significance established for month 3).

Secondary efficacy endpoints

Erenumab 70 mg was statistically superior to placebo for the key secondary endpoints of at least a 50% reduction in MMD and change in monthly MSMD (Table 2; p ≤ 0.01 for both) (Figures 1 and 2). A ≥ 50% reduction in MMD was achieved by 39.7% and 29.5% in the erenumab and placebo groups (odds ratio: 1.59; p = 0.010). Monthly MSMD was reduced by LSM −1.2 and −0.6 medication days, respectively (p = 0.002). In an ad hoc assessment among only those patients with baseline acute migraine-specific medication use, monthly MSMD was reduced by LSM −2.1 and −1.2, respectively (p = 0.002).

Figure 2.

Responder rates over time. Proportions of patients who achieved ≥ 50% reduction in monthly migraine days (MMD) from baseline during the double-blind treatment phase. Data were analyzed using imputation of missing data as non-response. Figure based on the efficacy analysis set. *p < 0.05 (statistical significance established for month 3).

Patient-reported outcome endpoints

With respect to patient-reported impact of migraine, differences in the proportion of patients who achieved ≥5-point reductions from baseline (improvement) in the two domains of the MPFID (pre-specified secondary endpoints) were not statistically significant between erenumab 70 mg and placebo (Table 2; p > 0.05). Respective ≥5-point reductions (improvement) in MPFID-PI in erenumab and placebo groups were achieved by 33.0% and 27.1% of patients (p = 0.13) and in MPFID-EA by 40.4% and 35.8% of patients (p = 0.26).

Prespecified, exploratory endpoints evaluated a series of PRO measures and their changes from baseline at month 3. Erenumab treatment was associated with improvements in health-related quality of life and clinically meaningful reductions in disability and headache impact when assessed using standard PRO instruments (Figure 3 and Table 3). At week 12, improvements in scores were greater in the erenumab group than in placebo in all three domains of the MSQ (role function-restrictive [MSQ-RFR], role function-preventive [MSQ-RFP], and emotional functioning [MSQ-EF]) (increase in scores indicates improvement) and HIT-6 (reduction in scores indicates improvement) (Figure 3 and Table 3) with treatment differences exceeding the established group-level minimally important difference (MID) for MSQ-RFR (≥3.2) and HIT-6 total score (≥1.5 points). Reductions from baseline to week 12 in modified (monthly) MIDAS total and presenteeism scores (for which no MID presently exists) were greater in the erenumab group as compared with placebo indicating greater improvement (Table 3). Reductions (improvement) from baseline to week 12 in the continuous MPFID-EA and MPFID-PI domain scores were numerically greater with erenumab 70 mg than placebo (Figure 3 and Table 3).

Figure 3.

Patient-reported outcomes over time. Least-squares mean changes from baseline in MSQ-RFR, MSQ-RFP, and MSQ-EF scores (Panel a), HIT-6 total scores (Panel b), and MPFID-PI and MPFID-EA scores (Panel c) among patients with episodic migraine who were assigned to receive erenumab 70 mg or placebo every month. The error bars represent 95% confidence intervals (95% CI). Figure based on the efficacy analysis set.

Table 3.

Exploratory PRO endpoints at week 12*.

	Placebo n = 288	Erenumab 70 mg n = 282	p value†
MPFID everyday activities
Baseline	13.1 ± 0.5	12.6 ± 0.5
Change from baseline	−3.2 ± 0.4	−4.33 ± 0.4
Difference from placebo (95% CI)		−1.1 (−2.3, 0.1)	0.061
MPFID physical impact
Baseline	11.4 ± 0.5	10.7 ± 0.5
Change from baseline	−1.9 ± 0.4	−3.18 ± 0.4
Difference from placebo (95% CI)		−1.3 (−2.4, −0.2)	0.021
MPFID overall impact on everyday activities
Baseline	13.6 ± 0.5	13.0 ± 0.5
Change from baseline	−3.13 ± 0.5	−4.51 ± 0.5
Difference from placebo (95% CI)		−1.4 (−2.6, −0.2)	0.028
HIT-6
Baseline score	59.5 ± 0.4	59.8 ± 0.3
Change from baseline	−2.6 ± 0.4	−4.9 ± 0.4
Difference from placebo (95% CI)		−2.3 (−3.3, −1.3)	<0.001
mMIDAS total
Baseline score	13.6 ± 0.7	14.1 ± 0.6
Change from baseline	−3.8 ± 0.5	−5.5 ± 0.5
Difference from placebo (95% CI)		−1.7 (−3.1, −0.3)	0.021
mMIDAS absenteeism
Baseline score	6.9 ± 0.4	7.4 ± 0.4
Change from baseline	−2.2 ± 0.3	−3.1 ± 0.3
Difference from placebo (95% CI)		−0.8 (−1.7, 0.0)	0.060
mMIDAS presenteeism
Baseline score	6.6 ± 0.4	6.6 ± 0.3
Change from baseline	−1.6 ± 0.3	−2.4 ± 0.3
Difference from placebo (95% CI)		−0.8 (−1.6, 0.1)	0.027
MSQ-RFR
Baseline	58.9 ± 1.0	57.9 ± 1.0
Change from baseline	9.7 ± 1.0	15.2 ± 1.0
Difference from placebo (95% CI)		5.5 (2.8, 8.2)	<0.001
MSQ-RFP
Baseline score	72.4 ± 1.2	70.5 ± 1.2
Change from baseline	8.4 ± 0.9	12.0 ± 0.9
Difference from placebo (95% CI)		3.6 (1.1, 6.0)	0.005
MSQ-EF
Baseline score	72.0 ± 1.4	70.5 ± 1.4
Change from baseline	7.3 ± 1.1	11.8 ± 1.1
Difference from placebo (95% CI)		4.5 (1.6, 7.4)	0.002

Data are least-squares means ± standard error unless otherwise indicated. Efficacy analysis set.

†

p values for pairwise comparison are unadjusted.

MPFID: Migraine Physical Function Impact Diary; HIT-6: Headache Impact Test; mMIDAS: Modified Migraine Disability Assessment; MSQ-RFR: Migraine-Specific Quality-of-Life Questionnaire role function-restrictive; MSQ-RFP: Migraine-Specific Quality-of-Life Questionnaire role function-preventive; MSQ-EF: Migraine-Specific Quality-of-Life Questionnaire emotional functioning; CI: confidence interval; HIT-6: Headache Impact Test-6; mMIDAS: modified Migraine Disability Assessment; MPFID: Migraine Physical Function Impact Diary; MSQ-EF: Migraine-Specific Quality-of-Life Questionnaire – emotional function; MSQ-RFP: Migraine-Specific Quality-of-Life Questionnaire – role function-preventive; MSQ-RFR: Migraine-Specific Quality-of-Life Questionnaire – role function-restrictive; PRO: patient-reported outcome.

Safety

The proportion of patients reporting at least one adverse event (AE) during the double-blind treatment phase was similar for the erenumab 70 mg and placebo groups (Table 4). Most common AEs (reported in ≥2% of patients in either group) were upper respiratory tract infection, injection site pain, influenza, fatigue, nausea, migraine, sinusitis, nasopharyngitis, and constipation (Table 4). One (0.3%) patient in the placebo group and five (1.8%) patients in the erenumab group experienced AEs that led to treatment discontinuation (Table 4). There were no clinically apparent differences in the type of serious AEs between the two treatment groups (Table 4) and no serious AE was reported by more than one patient within a treatment group during the double-blind treatment phase. No deaths occurred during the double-blind treatment phase. Twelve (4.3%) erenumab-treated patients developed anti-erenumab–binding antibodies through week 12, one of whom tested transiently positive for neutralizing antibodies at week 4, but negative for neutralizing antibodies at each subsequent visit. One patient was anti-erenumab binding antibody positive at baseline. No clinically significant changes in serum chemistry, hematology laboratory values, electrocardiogram (ECG), or vital signs were observed.

Table 4.

Adverse events through week 12.

	Placebo n = 289	Erenumab 70 mg n = 283
	no (%)	no (%)
Overall adverse events
Any	158 (54.7)	136 (48.1)
Serious*	5 (1.7)	3 (1.1)
Fatal	0 (0.0)	0 (0.0)
Discontinuation of study drug†	1 (0.3)	5 (1.8)
Grade 3‡	8 (2.8)	6 (2.1)
Common adverse events (reported in ≥2% of patients in any group)
Upper respiratory tract infection	14 (4.8)	18 (6.4)
Injection site pain	12 (4.2)	17 (6.0)
Nasopharyngitis	17 (5.9)	15 (5.3)
Influenza	10 (3.5)	11 (3.9)
Fatigue	6 (2.1)	10 (3.5)
Nausea	13 (4.5)	7 (2.5)
Migraine	8 (2.8)	6 (2.1)
Sinusitis	6 (2.1)	6 (2.1)
Constipation	6 (2.1)	4 (1.4)
Serious adverse events
Migraine	1 (0.3)	1 (0.4)
Intervertebral disc protrusion	0 (0.0)	1 (0.4)
Urinary tract infection	0 (0.0)	1 (0.4)
Cholecystitis acute	1 (0.3)	0 (0.0)
Flank pain	1 (0.3)	0 (0.0)
Hypersensitivity	1 (0.3)	0 (0.0)
Hyponatremia	1 (0.3)	0 (0.0)
Uterine leiomyoma	1 (0.3)	0 (0.0)

A serious adverse event was defined as an event that was fatal or life threatening, required inpatient hospitalization or prolongation of existing hospitalization, caused persistent or substantial disability or incapacity, caused congenital anomaly or birth defect, or was considered by the investigator to be medically important. Serious adverse events, all single events, were migraine, cholecystitis acute, flank pain, hypersensitivity, hyponatremia, and uterine leiomyoma in the placebo group and migraine, intervertebral disc protrusion, and urinary tract infection in the erenumab group.

†

Adverse events leading to discontinuation of study drug were irritable bowel syndrome, fatigue, allergy to arthropod sting, affect lability, and mechanical urticaria.

‡

The severity of adverse events was graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.03. No adverse events greater than grade 3 were reported.

Discussion

Erenumab treatment resulted in reduction in migraine frequency, use of acute migraine abortive medications, disability, and headache impact. Erenumab demonstrated superior efficacy to placebo for the primary endpoint (change from baseline in MMD at month 3) at a dose of 70 mg monthly, which had been established as the minimally effective dose in the EM population (14). In addition to the reduction in MMD, erenumab treatment resulted in reduced MSMD (triptans and ergotamine derivatives) and significantly greater odds of achieving at least a 50% reduction in MMD compared with placebo at month 3. The treatment effects on reduction of MMD and MSMD were apparent from the first planned time point (4 weeks) of analysis and were maintained throughout the double-blind phase (Figure 1). The least-squares difference versus placebo in monthly MSMD at month 3 (−0.6 days) was based on the total study population, which included 39% of patients who did not use acute migraine-specific medication during the baseline phase (Table 1) and therefore may underestimate the effect of erenumab in reducing the consumption of acute migraine-specific medication. When only users of acute migraine-specific medications at baseline were considered, the actual change from baseline in MSMD was −0.92 days.

These efficacy results are consistent with the results of a phase 2 erenumab study in EM testing doses as high as 70 mg, which showed a reduction of 3.4 MMD in the 70 mg erenumab group compared with 2.3 days for placebo (a placebo-adjusted reduction from baseline of 1.1 days) (14). In the STRIVE phase 3 trial in EM, which tested 70 mg and 140 mg erenumab doses, at 3 months there was a reduction in MMD of 3.0, 3.5, and 1.7 in the erenumab 70 mg, 140 mg, and placebo groups respectively (a placebo-adjusted reduction from baseline of 1.3 and 1.8 days) (27). The STRIVE trial had a 6-month double-blind phase, with reductions in MMD in the last 3 months of the 6-month double-blind treatment phase (i.e. the average over months 4 to 6) of 3.2 and 3.7 days in the erenumab 70 and 140 mg groups compared with 1.8 days for placebo (27). The magnitude of these placebo-adjusted treatment effects is dependent in part on the placebo response rates, which are known to be high in clinical trials of patients with migraine (28,29).

To help determine the meaningfulness of the treatment difference in reduced migraine frequency, it is important to measure patient-reported assessments of migraine impact to provide insight into patient perception of erenumab’s treatment effect. Supporting the patient perspective of the response to erenumab, the observed reductions in MMD were accompanied by reductions in the patient-reported outcomes assessed by standard PRO instruments such as HIT-6, modified (monthly) MIDAS, and MSQ. The differences in MSQ-RFR and HIT-6 total score exceeded the established group-level minimally important difference (MID). These PRO results underline the benefit obtained with erenumab compared to placebo in terms of meaningful improvements in terms of headache impact.

The MPFID is a novel migraine-specific instrument developed and validated to assess the impact of migraine on physical function, both on days with and without migraine. In contrast to standard headache PRO instruments, it is assessed daily with an electronic diary, and for any given month an average score is derived for each patient. Work is ongoing to establish the MID for change in MPFID domain scores. As an initial assessment, the current study used a categorical analysis based on a 5-point threshold change in MPFID-EA or MPFID-PI domain scores. However, a high proportion of the patients in the study population had scores <5 at baseline, limiting the sensitivity of the analysis. The results of the analysis assessed as continuous scores are consistent with the results in STRIVE, in which the mean between-group changes in MPFID domain scores were statistically significant (secondary endpoints in that study) (27). Further work is needed to determine the optimal approach to assessing change on the MPFID.

Our decision to use a dosage of 70 mg erenumab monthly in this study was based on the results of our phase 2 study in EM (14). A higher dosage of erenumab was examined in the STRIVE phase 3 pivotal study, which assessed both 70 mg and 140 mg monthly erenumab treatment over 6 months, and additional efficacy was apparent with the higher 140 mg dosage across the primary and secondary endpoints, and at all time points (27).

Overall, the incidence of adverse events was similar in the erenumab and placebo groups, and these analyses did not suggest any particular safety risk with erenumab administration. In line with the good safety and tolerability profile, the double-blind treatment phase completion rate was almost 95%, considerably higher than those observed for oral preventive migraine treatments, such as topiramate (30,31). As expected, given the non-hepatic metabolism of monoclonal antibodies, erenumab treatment did not result in any observable effect on liver enzymes, in contrast to the hepatotoxicity observed with small molecule CGRP receptor antagonists such as telcagepant (MK-0974) (32), which is thought to be due to off-target effects of the small molecules and not due to CGRP receptor inhibition. The rate of binding antibodies against erenumab was low (4.3% of subjects exposed) and only one subject (0.4%) was transiently positive for neutralizing antibodies (testing negative at the end of the study). Data from other studies with erenumab similarly indicate that anti-erenumab antibodies occur infrequently, do not increase over time, and remit in the majority of cases (14,15,27). Given the low frequency of anti-erenumab antibodies in individual studies and their frequently transient nature, the incidence and potential impact of anti-erenumab antibodies will be the subject of a future publication, using pooled data across erenumab studies.

Because CGRP is among a number of mediators with vasodilatory properties (e.g. substance P, neurokinins, nitric oxide) released during ischemia (33), there is a theoretical risk that patients with cardiovascular conditions might be at increased risk with inhibition of the CGRP pathway. However, during the 12-week double-blind phase, the occurrence of cardiovascular adverse events was low and did not substantially differ between erenumab and placebo groups (0.4% vs. 1.0%). These results supplement those from a placebo-controlled study of erenumab in a high risk population of patients with stable angina with a median age of 65 years, in which inhibition of the canonical CGRP receptor with erenumab did not adversely affect total exercise time in a treadmill test, among other safety endpoints (34). A lack of cardiovascular effects with inhibition of the CGRP receptor is also supported by studies with small-molecule CGRP receptor antagonists in which there is no evidence of vasoconstriction after CGRP receptor blockade when used for acute migraine relief (35,36). More data from migraine patients with comorbid cardiovascular conditions in a real-world setting may help further assess the theoretical cardiovascular risk of blocking the CGRP pathway.

With 69 sites in eight countries in North America and Europe, the ARISE study included a large, diverse population representative of the population with EM in these regions. However, further studies in a real-world setting may be required to determine the efficacy of erenumab in more diverse patient populations, including patients with no therapeutic response to multiple preventive medication categories who were not allowed into this study. Beyond the 3-month tolerability and safety data presented here, the 28-week open-label extension phase of this study will provide additional mid-term safety data on patients treated up to 40 weeks during the study. However, longer follow-up periods in large numbers of patient will be necessary to detect rare AEs and fully understand the safety profile of erenumab. Lastly, durability of the treatment effect will require longer studies, as this is not adequately assessed in a 3-month study.

There remains a considerable unmet need for safe and well-tolerated treatment options for the prevention of migraine that are more effective and have better tolerability than currently available preventive treatment options, as this can enable treatment adherence.

These results, together with other phase 2 and 3 studies of erenumab in episodic and chronic migraine (14,37), support the use of erenumab as a migraine preventive treatment. Compared to currently available therapies, the good safety and tolerability profile of erenumab may help promote better adherence to treatment in a condition with high unmet needs.

Clinical implications

Erenumab is a fully human monoclonal antibody that targets and blocks the canonical CGRP receptor.

Erenumab treatment resulted in reductions in monthly migraine days, increases in the proportion of patients achieving at least a 50% reduction from baseline in monthly migraine days, and reductions in the number of days per month that acute migraine-specific drugs were used.

This phase 3 study provides evidence that once-monthly subcutaneous injection of erenumab is a potential new preventive therapy in patients with episodic migraine.

Supplemental Material

Supplemental material for ARISE: A Phase 3 randomized trial of erenumab for episodic migraine

Supplemental material for ARISE: A Phase 3 randomized trial of erenumab for episodic migraine by David W Dodick, Messoud Ashina, Jan Lewis Brandes, David Kudrow, Michel Lanteri-Minet, Vera Osipova, Kerry Palmer, Hernan Picard, Daniel D Mikol and Robert A Lenz in Cephalalgia

Supplemental Material

Supplemental Figures - Supplemental material for ARISE: A Phase 3 randomized trial of erenumab for episodic migraine

Supplemental material, Supplemental Figures for ARISE: A Phase 3 randomized trial of erenumab for episodic migraine by David W Dodick, Messoud Ashina, Jan Lewis Brandes, David Kudrow, Michel Lanteri-Minet, Vera Osipova, Kerry Palmer, Hernan Picard, Daniel D Mikol and Robert A Lenz in Cephalalgia

Footnotes

Acknowledgements

The ARISE trial was funded by Amgen. Erenumab is co-developed in partnership with Amgen and Novartis. We thank the study investigators for the ARISE trial and patients for their participation and commitment to this work. Medical writing support was provided by Jon Nilsen, PhD, of Amgen.

Declaration of conflicting interests

The authors declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: David W Dodick has served and has been compensated for his role on advisory boards and/or has consulted within the past 5 years for Allergan, Amgen, Alder, Arteaus, Pfizer, Colucid, Merck, NuPathe, Eli Lilly and Company, Autonomic Technologies, Ethicon J&J, Zogenix, Supernus, Labrys, Boston Scientific, Medtronic, St Jude, Bristol-Myers Squibb, Lundbeck, Impax, MAP, Electrocore, Tonix, Novartis, Teva, Alcobra, Zosano, Insys, GBS/Nocira, Acorda, eNeura, Charleston Laboratories, Gore, Biohaven, Bioventric, Magellan, Theranica, Xenon, Dr Reddy’s/Promius Pharma. Dr Dodick owns equity in Epien, GBS/Nocira, Second Opinion, Healint, and Theranica. Dr Dodick has received funding for travel, speaking, editorial activities, or royalty payments from IntraMed, SAGE Publishing, Sun Pharma, Allergan, Oxford University Press, American Academy of Neurology, American Headache Society, West Virginia University Foundation, Canadian Headache Society, Healthlogix, Universal Meeting Management, WebMD, UptoDate, Medscape, Oregon Health Science Center, Starr Clinical, Decision Resources, Synergy, MedNet LLC, Peer View Institute for Medical Education, Medicom, Chameleon Communications, Academy for Continued Healthcare Learning, Haymarket Medical Education, Global Scientific Communications, HealthLogix, Miller Medical, MeetingLogiX, Wiley Blackwell, SAGE publishing, Cambridge University Press. Consulting use agreement: NeuroAssessment Systems, Myndshft. Board position: King-Devick Technologies, Inc. Epien Inc. Patent 17189376.1-1466: Title: Botulinum Toxin Dosage Regimen for Chronic Migraine Prophylaxis. Messoud Ashina: Personal fees from Alder BioPharmaceuticals, Allergan, Amgen, Alder, ATI, Eli Lilly, Novartis and Teva. Principal investigator for Alder ALD403-CLIN-011 (Phase 3b), Amgen 20120178 (Phase 2), 20120295 (Phase 2), 20130255 (OLE), 20120297 (Phase 3), GM-11 gamma-Core-R trials, Novartis CAMG334a2301 (Phase 3b), and PAC1 20150308 (Phase 2a). Jan Lewis Brandes: Research grants from Allergan, Amgen, Clinivest, Teva, CoLucid, Zozano, Arteus; Consulting fees from Amgen, Supernus, Promius; Speakers’ bureau fees from Amgen, Supernus, Promius, Depomed, Pernix, Teva, Avanir; Advisory board for Amgen, Avanir, Supernus, Teva, Lilly, Promius. David Kudrow: Personal fees from Amgen, Ely Lilly, Novartis, Alder. Research support from Alder, Ely Lilly, Amgen, Teva, Allergan, CoLucid, Zosano, Genentech-Roche, VMBiopharma, UCB.

Michel Lanteri-Minet: Received honoraria for advisory boards, speaker panels or investigation studies from Allergan, Amgen, Astellas, ATI, BMS, Boehringer, Boston Scientific, CoLucid, Convergence, Glaxo-SmithKline, Grunenthal, Lilly, Medtronic, Menarini, MSD, Novartis, Pfizer, ReckittBenckiser, Saint-Jude, Sanofi-Aventis, Teva, UCB, Zambon. Vera Osipova: Personal fees from Allergan, Pfizer and Takeda. Principal investigator for Amgen 20120297 (Phase 2). Kerry Palmer, Hernan Picard, Daniel D Mikol, and Robert A Lenz are employees and stockholders of Amgen Inc.

Funding

The authors received no financial support for the research, authorship, and/or publication of this article.

References

Lipton

Bigal

Diamond

et al.

Migraine prevalence, disease burden, and the need for preventive therapy. Neurology 2007; 68: 343–349.

Dodick

Loder

Manack Adams

et al.

Assessing barriers to chronic migraine consultation, diagnosis, and treatment: Results from the Chronic Migraine Epidemiology and Outcomes (CaMEO) study. Headache 2016; 56: 821–834.

Goadsby

Sprenger

. Current practice and future directions in the prevention and acute management of migraine. Lancet Neurol 2010; 9: 285–298.

Hepp

Bloudek

Varon

. Systematic review of migraine prophylaxis adherence and persistence. J Manag Care Pharm 2014; 20: 22–33.

Seng

Rains

Nicholson

et al.

Improving medication adherence in migraine treatment. Curr Pain Headache Rep 2015; 19: 24–24.

Edvinsson

Goadsby

. CGRP and its receptors provide new insights into migraine pathophysiology. Nat Rev Neurol 2010; 6: 573–582.

Edvinsson

Ekman

Jansen

et al.

Calcitonin gene-related peptide and cerebral blood vessels: distribution and vasomotor effects. J Cereb Blood Flow Metab 1987; 7: 720–728.

Goadsby

Edvinsson

Ekman

. Release of vasoactive peptides in the extracerebral circulation of humans and the cat during activation of the trigeminovascular system. Ann Neurol 1988; 23: 193–196.

Ashina

Bendtsen

Jensen

et al.

Plasma levels of calcitonin gene-related peptide in chronic tension-type headache. Neurology 2000; 55: 1335–1340.

10.

Lassen

Haderslev

Jacobsen

et al.

CGRP may play a causative role in migraine. Cephalalgia 2002; 22: 54–61.

11.

Bigal

Dodick

Rapoport

et al.

Safety, tolerability, and efficacy of TEV-48125 for preventive treatment of high-frequency episodic migraine: A multicentre, randomised, double-blind, placebo-controlled, phase 2b study. Lancet Neurol 2015; 14: 1081–1090.

12.

Dodick

Goadsby

Silberstein

et al.

Safety and efficacy of ALD403, an antibody to calcitonin gene-related peptide, for the prevention of frequent episodic migraine: A randomised, double-blind, placebo-controlled, exploratory phase 2 trial. Lancet Neurol 2014; 13: 1100–1107.

13.

Dodick

Goadsby

Spierings

et al.

Safety and efficacy of LY2951742, a monoclonal antibody to calcitonin gene-related peptide, for the prevention of migraine: A phase 2, randomised, double-blind, placebo-controlled study. Lancet Neurol 2014; 13: 885–892.

14.

Sun

Dodick

Silberstein

et al.

Safety and efficacy of AMG 334 for prevention of episodic migraine: A randomised, double-blind, placebo-controlled, phase 2 trial. Lancet Neurol 2016; 15: 382–390.

15.

Tepper

Ashina

Brandes

. Safety and efficacy of erenumab for preventive treatment of chronic migraine: A randomised, double-blind, placebo-controlled phase 2 trial. Lancet Neurol 2017; 16: 425–434.

16.

Shi

Rao

et al.

AMG 334, the first potent and selective human monoclonal antibody antagonist against the CGRP receptor. J Headache Pain 2014; 15: G43–G43.

17.

Shi

Lehto

Zhu

et al.

Pharmacologic characterization of AMG 334, a potent and selective human monoclonal antibody against the calcitonin gene-related peptide receptor. J Pharmacol Exp Ther 2016; 356: 223–231.

18.

Headache Classification Committee of the International Headache Society. International Classification of Headache Disorders, 3rd edition (beta version). Cephalalgia 2013; 33: 629–808.

19.

Kawata

Hsieh

Bender

et al.

Psychometric evaluation of a novel instrument assessing the impact of migraine on physical functioning: The Migraine Physical Function Impact Diary. Headache 2017; 57: 1385–1398.

20.

Dowson

. Assessing the impact of migraine. Curr Med Res Opin 2001; 17: 298–309.

21.

Kosinski

Bayliss

Bjorner

et al.

A six-item short-form survey for measuring headache impact: The HIT-6. Qual Life Res 2003; 12: 963–974.

22.

Stewart

Lipton

Dowson

et al.

Development and testing of the Migraine Disability Assessment (MIDAS) Questionnaire to assess headache-related disability. Neurology 2001; 56: S20–S28.

23.

Jhingran

Davis

LaVange

et al.

MSQ: Migraine-Specific Quality of Life Questionnaire. Further investigation of the factor structure. Pharmacoeconomics 1998; 13: 707–717.

24.

Jhingran

Osterhaus

Miller

et al.

Development and validation of the Migraine-Specific Quality of Life Questionnaire. Headache 1998; 38: 295–302.

25.

Goux S, Vass H, Lehman C, et al. MedDRA Maintenance and Support Services Organization Annual Report 2014. https://www.meddra.org/sites/default/files/page/documents/msso_annual_report_2014_english.pdf (2014, accessed 1 November 2017).

26.

U.S Department of Health and Human Services NIoH NCI. Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0. https://ctep.cancer.gov/protocoldevelopment/electronic_applications/docs/CTCAE_4.03.xlsx (2010, accessed 1 November 2017).

27.

Goadsby

Reuter

Hallstrom

et al.

A controlled trial of erenumab for episodic migraine. N Engl J Med 2017; 377: 2123–2132.

28.

Macedo

Baños

J-E

Farré

. Placebo response in the prophylaxis of migraine: A meta-analysis. Eur J Pain 2008; 12: 68–75.

29.

Van Der Kuy

Lohman

. A quantification of the placebo response in migraine prophylaxis. Cephalalgia 2002; 22: 265–270.

30.

Adelman

Freitag

Lainez

et al.

Analysis of safety and tolerability data obtained from over 1,500 patients receiving topiramate for migraine prevention in controlled trials. Pain Med 2008; 9: 175–185.

31.

Brandes

Saper

Diamond

et al.

Topiramate for migraine prevention: A randomized controlled trial. JAMA 2004; 291: 965–973.

32.

Connor

Zhang

et al.

Randomized controlled trial of the CGRP receptor antagonist telcagepant for migraine prevention. Neurology 2014; 83: 958–966.

33.

Burley

Ferdinandy

Baxter

. Cyclic GMP and protein kinase-G in myocardial ischaemia-reperfusion: Opportunities and obstacles for survival signaling. Br J Pharmacol 2007; 152: 855–869.

34.

Depre C, Antalik L, Starling A, et al. A randomized, double-blind, placebo-controlled study to evaluate the effect of erenumab on exercise time during a treadmill test in patients with stable angina (abstract). In: Proceedings of the 18th Congress of the International Headache Society. Vancouver, Canada. Cephalalgia 2017; 37(Suppl 1): 319–374.

35.

Petersen

Birk

Lassen

et al.

The CGRP-antagonist, BIBN4096BS does not affect cerebral or systemic haemodynamics in healthy volunteers. Cephalalgia 2005; 25: 139–147.

36.

Van der Schueren

Blanchard

Murphy

et al.

The potent calcitonin gene-related peptide receptor antagonist, telcagepant, does not affect nitroglycerin-induced vasodilation in healthy men. Brit J Clin Pharm 2011; 71: 708–717.

37.

Tepper

Ashina

Reuter

et al.

Safety and efficacy of erenumab for preventive treatment of chronic migraine: A randomised, double-blind, placebo-controlled phase 2 trial. Lancet Neurol 2017; 16: 425–434.

Supplementary Material

Please find the following supplemental material available below.

For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.

For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.

0.00 MB

0.09 MB

0.37 MB