Trial Outcomes & Findings for A Study of Galcanezumab (LY2951742) in Adults With Treatment-Resistant Migraine (NCT NCT03559257)
NCT ID: NCT03559257
Last Updated: 2020-07-08
Results Overview
Migraine Headache Day (MHD): A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean is derived from the average of months 1 to 3 from mixed model repeated measures (MMRM) model. Least square (LS) Mean was calculated using MMRM model with treatment, pooled country, month, treatment by month, baseline, and baseline by month as fixed effects.
COMPLETED
PHASE3
463 participants
Baseline, Month 1 through Month 3
2020-07-08
Participant Flow
Participant milestones
| Measure |
Placebo/Galcanezumab 120mg
Participants received matching placebo every month for three months by subcutaneous injection (SC) during double blind treatment phase. Participants received initial loading dose of 240mg galcanezumab followed by 120mg every month for two months by SC injection during open label treatment period.
|
Galcanezumab 120mg
Participants received initial loading dose of 240mg of galcanezumab followed by 120mg galcanezumab every month for two months by SC injection during double blind treatment period. Participants received 120mg of galcanezumab every month for three months by SC injection during open label treatment period.
|
|---|---|---|
|
Double Blind Treatment Period
STARTED
|
230
|
233
|
|
Double Blind Treatment Period
Received at Least One Dose of Study Drug
|
230
|
232
|
|
Double Blind Treatment Period
COMPLETED
|
226
|
225
|
|
Double Blind Treatment Period
NOT COMPLETED
|
4
|
8
|
|
Open-label Treatment Period
STARTED
|
225
|
224
|
|
Open-label Treatment Period
COMPLETED
|
215
|
217
|
|
Open-label Treatment Period
NOT COMPLETED
|
10
|
7
|
Reasons for withdrawal
| Measure |
Placebo/Galcanezumab 120mg
Participants received matching placebo every month for three months by subcutaneous injection (SC) during double blind treatment phase. Participants received initial loading dose of 240mg galcanezumab followed by 120mg every month for two months by SC injection during open label treatment period.
|
Galcanezumab 120mg
Participants received initial loading dose of 240mg of galcanezumab followed by 120mg galcanezumab every month for two months by SC injection during double blind treatment period. Participants received 120mg of galcanezumab every month for three months by SC injection during open label treatment period.
|
|---|---|---|
|
Double Blind Treatment Period
Withdrawal by Subject
|
2
|
1
|
|
Double Blind Treatment Period
Protocol Violation
|
1
|
4
|
|
Double Blind Treatment Period
Lack of Efficacy
|
1
|
1
|
|
Double Blind Treatment Period
Adverse Event
|
0
|
1
|
|
Double Blind Treatment Period
Screen Failure
|
0
|
1
|
|
Open-label Treatment Period
Adverse Event
|
1
|
4
|
|
Open-label Treatment Period
Lack of Efficacy
|
3
|
2
|
|
Open-label Treatment Period
Withdrawal by Subject
|
3
|
0
|
|
Open-label Treatment Period
Protocol Violation
|
2
|
0
|
|
Open-label Treatment Period
Lost to Follow-up
|
1
|
0
|
|
Open-label Treatment Period
Physician Decision
|
0
|
1
|
Baseline Characteristics
A Study of Galcanezumab (LY2951742) in Adults With Treatment-Resistant Migraine
Baseline characteristics by cohort
| Measure |
Placebo/Galcanezumab 120mg
n=230 Participants
Participants received matching placebo every month for three months by subcutaneous injection (SC) during double blind treatment phase. Participants received initial loading dose of 240mg galcanezumab followed by 120mg every month for two months by SC injection during open label treatment period.
|
Galcanezumab 120mg
n=232 Participants
Participants received initial loading dose of 240mg of galcanezumab followed by 120mg galcanezumab every month for two months by SC injection during double blind treatment period. Participants received 120mg of galcanezumab every month for three months by SC injection during open label treatment period.
|
Total
n=462 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
45.67 years
STANDARD_DEVIATION 12.33 • n=99 Participants
|
45.87 years
STANDARD_DEVIATION 11.34 • n=107 Participants
|
45.77 years
STANDARD_DEVIATION 11.83 • n=206 Participants
|
|
Sex: Female, Male
Female
|
202 Participants
n=99 Participants
|
195 Participants
n=107 Participants
|
397 Participants
n=206 Participants
|
|
Sex: Female, Male
Male
|
28 Participants
n=99 Participants
|
37 Participants
n=107 Participants
|
65 Participants
n=206 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
16 Participants
n=99 Participants
|
15 Participants
n=107 Participants
|
31 Participants
n=206 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
174 Participants
n=99 Participants
|
172 Participants
n=107 Participants
|
346 Participants
n=206 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
40 Participants
n=99 Participants
|
45 Participants
n=107 Participants
|
85 Participants
n=206 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
1 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Asian
|
35 Participants
n=99 Participants
|
37 Participants
n=107 Participants
|
72 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=99 Participants
|
1 Participants
n=107 Participants
|
1 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Black or African American
|
2 Participants
n=99 Participants
|
3 Participants
n=107 Participants
|
5 Participants
n=206 Participants
|
|
Race (NIH/OMB)
White
|
182 Participants
n=99 Participants
|
183 Participants
n=107 Participants
|
365 Participants
n=206 Participants
|
|
Race (NIH/OMB)
More than one race
|
3 Participants
n=99 Participants
|
0 Participants
n=107 Participants
|
3 Participants
n=206 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
7 Participants
n=99 Participants
|
8 Participants
n=107 Participants
|
15 Participants
n=206 Participants
|
|
Monthly Migraine Headache Days
|
13.01 Days
STANDARD_DEVIATION 5.73 • n=99 Participants
|
13.44 Days
STANDARD_DEVIATION 6.08 • n=107 Participants
|
13.23 Days
STANDARD_DEVIATION 5.91 • n=206 Participants
|
PRIMARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized participants who received at least one dose of study drug and had baseline and at least one post baseline value.
Migraine Headache Day (MHD): A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean is derived from the average of months 1 to 3 from mixed model repeated measures (MMRM) model. Least square (LS) Mean was calculated using MMRM model with treatment, pooled country, month, treatment by month, baseline, and baseline by month as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=228 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=230 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Overall Mean Change From Baseline in the Number of Monthly Migraine Headache Days
|
-1.02 Days
Standard Error 0.32
|
-4.14 Days
Standard Error 0.32
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized episodic migraine participants who received at least one dose of study drug and had baseline and at least one post baseline value.
MHD: A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean is derived from the average of months 1 to 3 from MMRM model. Least square (LS) Mean was calculated using MMRM model with treatment, pooled country, month, treatment by month, baseline, and baseline by month as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=132 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=137 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Overall Mean Change From Baseline in the Number of Monthly Migraine Headache Days in Participants With Episodic Migraine
|
-0.31 Days
Standard Error 0.34
|
-2.88 Days
Standard Error 0.34
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized participants who received at least one dose of study drug and had baseline and at least one post baseline value.
MHD: A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean percentage across months 1 through 3 of patients with at least a 50% reduction in monthly MHDs from baseline using a categorical pseudo likelihood-based repeated measures model for binary responder indicator with fixed, categorical effects of treatment, month, treatment by month, and continuous, fixed covariate of baseline monthly MHD.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=228 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=230 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Percentage of Participants With ≥50% Reduction From Baseline in Monthly Migraine Headache Days
|
13.3 Percentage of Participants
Interval 10.2 to 17.3
|
37.7 Percentage of Participants
Interval 32.9 to 42.8
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized episodic migraine participants who received at least one dose of study drug and had baseline and at least one post baseline value.
MHD: A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean percentage across months 1 through 3 of patients with at least a 50% reduction in monthly MHDs from baseline using a categorical pseudo likelihood-based repeated measures model for binary responder indicator with fixed, categorical effects of treatment, month, treatment by month, and continuous, fixed covariate of baseline monthly MHD.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=132 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=137 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Percentage of Participants With Episodic Migraine With ≥50% Reduction From Baseline in Monthly Migraine Headache Days
|
17.1 Percentage of Participants
Interval 12.7 to 22.7
|
41.8 Percentage of Participants
Interval 35.7 to 48.1
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3. LS Mean was calculated using MMRM model with treatment, pooled country, month, treatment by month, baseline, and baseline by month as fixed effects.
MSQ v2.1 is a health status instrument, with a 4-week recall period, developed to address physical and emotional limitations of specific concern to individuals with migraine. Addressing the impact of migraine on work or daily activities, relationships with family \& friends, leisure time, productivity, concentration, energy, tiredness \& feelings. It consists of 14 items that address 3 domains:(1) Role Function-Restrictive (items 1-7);(2) Role Function- Preventive (items 8-11);\&(3) Emotional Function (items 12-14).Response options range from "none of the time" (value 1) to "all of the time" (value 6),\& are reverse-recoded (value 6 to 1) before the domain scores are calculated. Total raw scores for each domain is the sum of the final item value for all of the items in that domain. After the total raw score is computed for each domain, they are transformed to a 0-100 scale with higher scores indicating a better health status \& a positive change in scores reflecting functional improvement.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=222 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=223 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the Role Function-Restrictive Domain Score of the Migraine-Specific Quality of Life Questionnaire Version 2.1 (MSQ v2.1)
|
10.68 score on a scale
Standard Error 1.34
|
23.21 score on a scale
Standard Error 1.35
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized episodic migraine participants who received at least one dose of study drug and had a post baseline value at Month 3. LS Mean was calculated using MMRM model with treatment, pooled country, month, treatment by month, baseline, and baseline by month as fixed effects.
MSQ v2.1 is a health status instrument, with a 4-week recall period, developed to address physical and emotional limitations of specific concern to individuals with migraine. Addressing the impact of migraine on work or daily activities, relationships with family \& friends, leisure time, productivity, concentration, energy, tiredness \& feelings. It consists of 14 items that address 3 domains:(1) Role Function-Restrictive (items 1-7);(2) Role Function- Preventive (items 8-11);\&(3) Emotional Function (items 12-14).Response options range from "none of the time" (value 1) to "all of the time" (value 6),\& are reverse-recoded (value 6 to 1) before the domain scores are calculated. Total raw scores for each domain is the sum of the final item value for all of the items in that domain. After the total raw score is computed for each domain, they are transformed to a 0-100 scale with higher scores indicating a better health status \& a positive change in scores reflecting functional improvement.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=127 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=135 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the Role Function-Restrictive Domain Score of the Migraine-Specific Quality of Life Questionnaire Version 2.1 (MSQ v2.1) in Participants With Episodic Migraine
|
11.88 score on a scale
Standard Error 1.80
|
23.39 score on a scale
Standard Error 1.79
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized episodic migraine participants who received at least one dose of study drug and had baseline and at least one post baseline value.
MHD: A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean percentage across months 1 through 3 of patients with at least a 75% reduction in monthly MHDs from baseline using a categorical pseudo likelihood-based repeated measures model for binary responder indicator with fixed, categorical effects of treatment, month, treatment by month, and continuous, fixed covariate of baseline monthly MHD.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=132 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=137 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Percentage of Participants With Episodic Migraine With ≥75% Reduction From Baseline in Monthly Migraine Headache Days
|
3.7 Percentage of Participants
Interval 1.6 to 8.2
|
18.4 Percentage of Participants
Interval 13.9 to 23.9
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized episodic migraine participants who received at least one dose of study drug and had baseline and at least one post baseline value.
MHD: A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean percentage across months 1 through 3 of patients with 100% reduction in monthly MHDs from baseline using a categorical pseudo likelihood-based repeated measures model for binary responder indicator with fixed, categorical effects of treatment, month, treatment by month, and continuous, fixed covariate of baseline monthly MHD.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=132 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=137 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Percentage of Participants With Episodic Migraine With 100% Reduction From Baseline in Monthly Migraine Headache Days
|
0.00 Percentage of Participants
Interval 0.0 to 0.0
|
7.7 Percentage of Participants
Interval 4.7 to 12.3
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized participants who received at least one dose of study drug and had baseline and at least one post baseline value.
MHD: A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean percentage across months 1 through 3 of patients with at least a 75% reduction in monthly MHDs from baseline using a categorical pseudo likelihood-based repeated measures model for binary responder indicator with fixed, categorical effects of treatment, month, treatment by month, and continuous, fixed covariate of baseline monthly MHD.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=228 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=230 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Percentage of Participants With ≥75% Reduction From Baseline in Monthly Migraine Headache Days
|
3.3 Percentage of Participants
Interval 1.7 to 6.3
|
14.5 Percentage of Participants
Interval 10.9 to 19.0
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized participants who received at least one dose of study drug and had baseline and at least one post baseline value.
MHD: A calendar day on which a migraine headache or probable migraine headache occurred. Overall mean percentage across months 1 through 3 of patients with 100% reduction in monthly MHDs from baseline using a categorical pseudo likelihood-based repeated measures model for binary responder indicator with fixed, categorical effects of treatment, month, treatment by month, and continuous, fixed covariate of baseline monthly MHD.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=228 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=230 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Percentage of Participants With 100% Reduction From Baseline in Monthly Migraine Headache Days
|
0.000 Percentage of Participants
Interval 0.0 to 0.0
|
4.9 Percentage of Participants
Interval 2.8 to 8.6
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized participants who received at least one dose of study drug and had baseline and at least one post baseline value.
Overall mean is derived from the average of months 1 to 3 from Mixed model repeated measures (MMRM) model. Least square (LS) Mean was calculated using MMRM model with treatment, pooled country, month, treatment by month, baseline, and baseline by month as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=228 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=230 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Overall Mean Change From Baseline in the Number of Monthly Days With Acute Headache Medication Use
|
-0.80 Days
Standard Error 0.31
|
-4.19 Days
Standard Error 0.32
|
SECONDARY outcome
Timeframe: Baseline, Month 1 through Month 3Population: All randomized participants who received at least one dose of study drug and had baseline and at least one post baseline value.
Headache Day: A calendar day on which any type of headache occurred (including migraine, probable migraine, and non-migraine headache). Overall mean is derived from the average of months 1 to 3 from MMRM model. Least square (LS) Mean was calculated using MMRM model with treatment, pooled country, month, treatment by month, baseline, and baseline by month as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=228 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=230 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Overall Mean Change From Baseline in the Number of Monthly Headache Days
|
-1.05 Days
Standard Error 0.36
|
-4.18 Days
Standard Error 0.35
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3.
The MIDAS is a participant-rated scale which was designed to quantify headache-related disability over a 3-month period. This instrument consists of five items that reflect the number of days reported as missed or with reduced productivity at work or home, and the number of days of missed social events. Each item has a numeric response range from 0 to 90 days, if days are missed from work or home they are not counted as days with reduced productivity at work or home. The numeric responses are summed to produce a total score ranging from 0 to 270, in which a higher value is indicative of more disability. LS mean was calculated using analysis of covariance (ANCOVA) with last observation carried forward (LOCF), with baseline, pooled country, baseline migraine frequency category, and treatment as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=225 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=228 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the Migraine Disability Assessment Test (MIDAS) Total Score
|
-3.295 score on a scale
Standard Error 3.2834
|
-21.097 score on a scale
Standard Error 3.3164
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3.
MIBS-4 is a self-administered scale that measures the burden related to headache in the time between attacks. The instrument consists of 4 items that address disruption at work and school, diminished family and social life, difficulty planning, and emotional difficulty. The questionnaire specifically asks about the effect of the disease over the past 4 weeks on days without a headache attack. Response options include: don't know/not applicable (0), never (0), rarely (1), some of the time (2), much of the time (3), or most or all of the time (3). Each responses associated numerical score are summed across all 4 items resulting in a total score ranging from 0 to 12, and the level of interictal burden being categorized into the following: 0 for none, 1-2 mild, 3-4 moderate, and \>5 severe. LS mean was calculated using MMRM model with fixed effects of treatment, pooled country, baseline migraine frequency category, month, treatment by month as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=222 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=223 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the 4-item Migraine Interictal Burden Scale (MIBS-4)
|
-0.78 score on a scale
Standard Error 0.21
|
-1.83 score on a scale
Standard Error 0.21
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3.
The WPAI Questionnaire is a patient-reported instrument developed to measure the impact on work productivity and regular activities attributable to a specific health problem (migraine). Recall period is the past 7 days. It contains 6 items that measure: 1) employment status, 2) hours missed from work due to the specific health problem, 3) hours missed from work for other reasons, 4) hours actually worked, 5) degree health affected productivity while working, and 6) degree health affected productivity in regular unpaid activities. Four scores are calculated from the responses to these 6 items: absenteeism, presenteeism, work productivity loss, and activity impairment. Scores are calculated as impairment percentages (0-100%), with higher numbers indicating greater impairment and less productivity, i.e, worse outcomes. LS mean was calculated using ANCOVA with LOCF with baseline, pooled country, baseline migraine frequency category, and treatment as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=225 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=227 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the Work Productivity and Activity Impairment Questionnaire (WPAI)
Presenteeism
|
-2.564 score on a scale
Standard Error 2.3222
|
-12.504 score on a scale
Standard Error 2.3705
|
|
Mean Change From Baseline in the Work Productivity and Activity Impairment Questionnaire (WPAI)
Activity Impairment
|
-8.644 score on a scale
Standard Error 1.9195
|
-20.713 score on a scale
Standard Error 1.9537
|
|
Mean Change From Baseline in the Work Productivity and Activity Impairment Questionnaire (WPAI)
Absenteeism
|
-2.900 score on a scale
Standard Error 1.2436
|
-4.224 score on a scale
Standard Error 1.2929
|
|
Mean Change From Baseline in the Work Productivity and Activity Impairment Questionnaire (WPAI)
Work Impairment
|
-3.457 score on a scale
Standard Error 2.4098
|
-14.307 score on a scale
Standard Error 2.5148
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3.
The PGI-S is a patient-rated instrument that measures illness severity. For this study, the patient was instructed as follows: "Considering migraine as a chronic condition, how would you rate your level of illness?" The PGI-S includes a range of possible responses, from 1 ("normal, not at all ill") to 7 ("extremely ill"). LS mean was calculated using ANCOVA with LOCF with baseline, pooled country, baseline migraine frequency category, and treatment as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=225 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=228 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the Patient Global Impression of Severity (PGI-S)
|
-0.283 score on a scale
Standard Error 0.0863
|
-0.664 score on a scale
Standard Error 0.0873
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3.
EQ-5D-5L is a 2-part questionnaire that assesses general health status for 'today'. The first part is comprised of the following 5 participant-reported dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems, and extreme problems. The responses are used to derive the health state index scores using country-specific algorithms, with scores ranging from less than 0 (where zero is a health state equivalent to death; negative values are valued as worse than dead) to 1 (perfect health). Index values were calculated using the US algorithm (-0.109 to 1). A higher score indicates better health state. LS mean was calculated using ANCOVA with LOCF with baseline, pooled country, baseline migraine frequency category, and treatment as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=225 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=227 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the European Quality of Life Questionnaire 5 Dimensions 5 Levels (EQ-5D-5L) - Health State Index (US)
|
-0.002 score on a scale
Standard Error 0.0079
|
0.013 score on a scale
Standard Error 0.0080
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3.
EQ-5D-5L is a 2-part questionnaire that assesses general health status for 'today'. The first part is comprised of the following 5 participant-reported dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems, and extreme problems. The responses are used to derive the health state index scores using country-specific algorithms, with scores ranging from less than 0 (where zero is a health state equivalent to death; negative values are valued as worse than dead) to 1 (perfect health). Index values were calculated using the UK algorithm (-0.594 to 1). LS mean was calculated using ANCOVA with LOCF with baseline, pooled country, baseline migraine frequency category, and treatment as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=225 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=227 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the European Quality of Life Questionnaire 5 Dimensions 5 Levels (EQ-5D-5L) - Health State Index (UK)
|
-0.001 score on a scale
Standard Error 0.0109
|
0.017 score on a scale
Standard Error 0.0110
|
SECONDARY outcome
Timeframe: Baseline, Month 3Population: All randomized participants who received at least one dose of study drug and had a post baseline value at Month 3.
EQ-5D-5L is a 2-part questionnaire that assesses general health status 'today'. . The second part is assessed using a visual analog scale (VAS) on which the patient rates their perceived health state, ranging from 0 (the worst health you can imagine) to 100 (the best health you can imagine). LS mean was calculated using ANCOVA with LOCF with baseline, pooled country, baseline migraine frequency category, and treatment as fixed effects.
Outcome measures
| Measure |
Placebo - Double-Blind Treatment Phase
n=225 Participants
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=227 Participants
Participants received initial loading dose of 240 milligrams (mg) of galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
|---|---|---|
|
Mean Change From Baseline in the European Quality of Life Questionnaire 5 Dimensions 5 Levels (EQ-5D-5L) - VAS Score
|
-0.086 mm
Standard Error 1.2916
|
3.376 mm
Standard Error 1.3080
|
Adverse Events
Placebo - Double-Blind Treatment Phase
Galcanezumab 120mg - Double-Blind Treatment Phase
Placebo/Galcanezumab 120mg - Open-Label Treatment Phase
Galcanezumab 120mg/Galcanezumab 120mg - Open-Label Treatment
Serious adverse events
| Measure |
Placebo - Double-Blind Treatment Phase
n=230 participants at risk
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=232 participants at risk
Participants received initial loading dose of 240 milligrams (mg) of Galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
Placebo/Galcanezumab 120mg - Open-Label Treatment Phase
n=225 participants at risk
Participants received initial loading dose of 240mg Galcanezumab followed by 120mg every month for two months by SC injection.
|
Galcanezumab 120mg/Galcanezumab 120mg - Open-Label Treatment
n=224 participants at risk
Participants received 120mg of Galcanezumab every month for three months by SC injection.
|
|---|---|---|---|---|
|
Gastrointestinal disorders
Haemorrhoids
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.43%
1/232 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/225 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Gastrointestinal disorders
Inguinal hernia
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.44%
1/225 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
General disorders
Asthenia
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/225 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.45%
1/224 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
General disorders
Pain
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.44%
1/225 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Infections and infestations
Pneumonia
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/225 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.45%
1/224 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Infections and infestations
Tonsillitis
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.43%
1/232 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/225 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Injury, poisoning and procedural complications
Arthropod bite
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.44%
1/225 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Injury, poisoning and procedural complications
Injury
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.44%
1/225 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Injury, poisoning and procedural complications
Lower limb fracture
|
0.43%
1/230 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/225 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Nervous system disorders
Hemiplegia
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.44%
1/225 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Reproductive system and breast disorders
Ovarian cyst ruptured
|
0.00%
0/202 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/195 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/197 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.53%
1/187 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Respiratory, thoracic and mediastinal disorders
Pulmonary embolism
|
0.00%
0/230 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.44%
1/225 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Vascular disorders
Behcet's syndrome
|
0.43%
1/230 • Number of events 1 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/232 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/225 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
0.00%
0/224 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
Other adverse events
| Measure |
Placebo - Double-Blind Treatment Phase
n=230 participants at risk
Participants received matching placebo every month for three months by SC injection.
|
Galcanezumab 120mg - Double-Blind Treatment Phase
n=232 participants at risk
Participants received initial loading dose of 240 milligrams (mg) of Galcanezumab followed by 120mg Galcanezumab every month for two months by SC injection.
|
Placebo/Galcanezumab 120mg - Open-Label Treatment Phase
n=225 participants at risk
Participants received initial loading dose of 240mg Galcanezumab followed by 120mg every month for two months by SC injection.
|
Galcanezumab 120mg/Galcanezumab 120mg - Open-Label Treatment
n=224 participants at risk
Participants received 120mg of Galcanezumab every month for three months by SC injection.
|
|---|---|---|---|---|
|
General disorders
Injection site pain
|
5.7%
13/230 • Number of events 30 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
2.2%
5/232 • Number of events 7 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
4.9%
11/225 • Number of events 19 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
2.2%
5/224 • Number of events 7 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
|
Infections and infestations
Nasopharyngitis
|
9.1%
21/230 • Number of events 24 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
6.9%
16/232 • Number of events 17 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
4.9%
11/225 • Number of events 11 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
3.6%
8/224 • Number of events 9 • Up to 6 months
Gender specific events only occurring in male or female participants have had the number of participants at risk adjusted accordingly.
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place
Restriction type: GT60