Trial Outcomes & Findings for A Study of Galcanezumab (LY2951742) in Participants With Migraine Headache (NCT NCT02163993)
NCT ID: NCT02163993
Last Updated: 2018-11-23
Results Overview
The criteria for a migraine headache was adapted from the standard International Headache Society (IHS) International Classification of Headache Disorders (ICHD)-3 beta. The definition of a migraine headache was a headache with or without aura, of ≥30 minutes (min) duration, and with both ("A" and "B") required features from the IHS ICHD-3 beta definition. Required feature "A" includes at least 2 of the following headache characteristics: unilateral location, pulsatile quality, moderate or severe pain intensity, or aggravation by or causing avoidance of routine physical activity. Required feature "B" includes at least 1 of the following during the headache: nausea and/or vomiting, or photophobia and phonophobia.
COMPLETED
PHASE2
414 participants
Baseline, 12 Weeks
2018-11-23
Participant Flow
Treatment period (0 to 12 weeks), Post-treatment period (12 to 24 weeks)
Participant milestones
| Measure |
Placebo
Placebo given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
5mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Treatment Period
STARTED
|
138
|
68
|
68
|
71
|
69
|
|
Treatment Period
Received at Least 1 Dose of Study Drug
|
137
|
68
|
68
|
70
|
67
|
|
Treatment Period
COMPLETED
|
126
|
59
|
66
|
62
|
62
|
|
Treatment Period
NOT COMPLETED
|
12
|
9
|
2
|
9
|
7
|
|
Post-treatment Period
STARTED
|
125
|
61
|
66
|
63
|
65
|
|
Post-treatment Period
COMPLETED
|
121
|
55
|
62
|
61
|
62
|
|
Post-treatment Period
NOT COMPLETED
|
4
|
6
|
4
|
2
|
3
|
Reasons for withdrawal
| Measure |
Placebo
Placebo given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
5mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Treatment Period
Adverse Event
|
0
|
1
|
0
|
0
|
1
|
|
Treatment Period
Lost to Follow-up
|
2
|
3
|
1
|
3
|
1
|
|
Treatment Period
Physician Decision
|
1
|
0
|
0
|
0
|
0
|
|
Treatment Period
Protocol Violation
|
2
|
1
|
0
|
1
|
2
|
|
Treatment Period
Withdrawal by Subject
|
6
|
4
|
1
|
4
|
1
|
|
Treatment Period
Not treated
|
1
|
0
|
0
|
1
|
2
|
|
Post-treatment Period
Adverse Event
|
0
|
0
|
1
|
0
|
0
|
|
Post-treatment Period
Lost to Follow-up
|
2
|
2
|
3
|
1
|
0
|
|
Post-treatment Period
Protocol Violation
|
0
|
0
|
0
|
0
|
1
|
|
Post-treatment Period
Withdrawal by Subject
|
2
|
4
|
0
|
1
|
2
|
Baseline Characteristics
A Study of Galcanezumab (LY2951742) in Participants With Migraine Headache
Baseline characteristics by cohort
| Measure |
Placebo
n=137 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=68 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=70 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=67 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
Total
n=410 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|---|
|
Age, Continuous
|
39.54 Years
STANDARD_DEVIATION 12.10 • n=39 Participants
|
41.40 Years
STANDARD_DEVIATION 11.15 • n=41 Participants
|
39.63 Years
STANDARD_DEVIATION 12.42 • n=35 Participants
|
40.57 Years
STANDARD_DEVIATION 10.92 • n=31 Participants
|
40.79 Years
STANDARD_DEVIATION 13.20 • n=146 Participants
|
40.24 Years
STANDARD_DEVIATION 11.96 • n=19 Participants
|
|
Sex: Female, Male
Female
|
109 Participants
n=39 Participants
|
55 Participants
n=41 Participants
|
61 Participants
n=35 Participants
|
59 Participants
n=31 Participants
|
56 Participants
n=146 Participants
|
340 Participants
n=19 Participants
|
|
Sex: Female, Male
Male
|
28 Participants
n=39 Participants
|
13 Participants
n=41 Participants
|
7 Participants
n=35 Participants
|
11 Participants
n=31 Participants
|
11 Participants
n=146 Participants
|
70 Participants
n=19 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
20 Participants
n=39 Participants
|
14 Participants
n=41 Participants
|
11 Participants
n=35 Participants
|
8 Participants
n=31 Participants
|
14 Participants
n=146 Participants
|
67 Participants
n=19 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
117 Participants
n=39 Participants
|
54 Participants
n=41 Participants
|
57 Participants
n=35 Participants
|
62 Participants
n=31 Participants
|
53 Participants
n=146 Participants
|
343 Participants
n=19 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
0 Participants
n=19 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
2 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
2 Participants
n=19 Participants
|
|
Race (NIH/OMB)
Asian
|
6 Participants
n=39 Participants
|
1 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
3 Participants
n=31 Participants
|
1 Participants
n=146 Participants
|
11 Participants
n=19 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
0 Participants
n=19 Participants
|
|
Race (NIH/OMB)
Black or African American
|
14 Participants
n=39 Participants
|
16 Participants
n=41 Participants
|
9 Participants
n=35 Participants
|
23 Participants
n=31 Participants
|
13 Participants
n=146 Participants
|
75 Participants
n=19 Participants
|
|
Race (NIH/OMB)
White
|
106 Participants
n=39 Participants
|
49 Participants
n=41 Participants
|
57 Participants
n=35 Participants
|
43 Participants
n=31 Participants
|
52 Participants
n=146 Participants
|
307 Participants
n=19 Participants
|
|
Race (NIH/OMB)
More than one race
|
9 Participants
n=39 Participants
|
2 Participants
n=41 Participants
|
2 Participants
n=35 Participants
|
1 Participants
n=31 Participants
|
1 Participants
n=146 Participants
|
15 Participants
n=19 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=39 Participants
|
0 Participants
n=41 Participants
|
0 Participants
n=35 Participants
|
0 Participants
n=31 Participants
|
0 Participants
n=146 Participants
|
0 Participants
n=19 Participants
|
|
Region of Enrollment
United States
|
137 Participants
n=39 Participants
|
68 Participants
n=41 Participants
|
68 Participants
n=35 Participants
|
70 Participants
n=31 Participants
|
67 Participants
n=146 Participants
|
410 Participants
n=19 Participants
|
|
Number of migraine headache days
|
6.64 Days
STANDARD_DEVIATION 2.73 • n=39 Participants
|
6.68 Days
STANDARD_DEVIATION 2.73 • n=41 Participants
|
6.41 Days
STANDARD_DEVIATION 2.66 • n=35 Participants
|
6.95 Days
STANDARD_DEVIATION 2.56 • n=31 Participants
|
6.73 Days
STANDARD_DEVIATION 2.48 • n=146 Participants
|
6.68 Days
STANDARD_DEVIATION 2.64 • n=19 Participants
|
|
Number of probable and migraine headache days
|
8.04 Days
STANDARD_DEVIATION 3.08 • n=39 Participants
|
8.55 Days
STANDARD_DEVIATION 3.23 • n=41 Participants
|
8.33 Days
STANDARD_DEVIATION 3.21 • n=35 Participants
|
8.69 Days
STANDARD_DEVIATION 3.46 • n=31 Participants
|
8.01 Days
STANDARD_DEVIATION 2.79 • n=146 Participants
|
8.28 Days
STANDARD_DEVIATION 3.15 • n=19 Participants
|
PRIMARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All participants with a valid 28-day baseline assessment of migraine headache days who received at least 1 dose of study treatment and had evaluable postbaseline headache data.
The criteria for a migraine headache was adapted from the standard International Headache Society (IHS) International Classification of Headache Disorders (ICHD)-3 beta. The definition of a migraine headache was a headache with or without aura, of ≥30 minutes (min) duration, and with both ("A" and "B") required features from the IHS ICHD-3 beta definition. Required feature "A" includes at least 2 of the following headache characteristics: unilateral location, pulsatile quality, moderate or severe pain intensity, or aggravation by or causing avoidance of routine physical activity. Required feature "B" includes at least 1 of the following during the headache: nausea and/or vomiting, or photophobia and phonophobia.
Outcome measures
| Measure |
Placebo
n=134 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=69 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Mean Change From Baseline in the Number of Migraine Headache Days in the Last 28-Day Period of the 12-Week Treatment Phase
|
-3.66 Days
Standard Deviation 0.28
|
-4.23 Days
Standard Deviation 0.37
|
-3.92 Days
Standard Deviation 0.36
|
-4.80 Days
Standard Deviation 0.37
|
-4.28 Days
Standard Deviation 0.39
|
SECONDARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All participants with a valid 28-day baseline assessment of migraine headache days who received at least 1 dose of study treatment and had evaluable postbaseline headache data.
A migraine attack was defined as beginning on any day a migraine headache day was recorded and ending when a migraine headache-free day occurred. The criteria was adapted from the standard IHS ICHD-3 beta definition. The definition of a migraine headache was a headache with or without aura, of ≥30 minutes (min) duration, and with both ("A" and "B") required features from the IHS ICHD-3 beta definition. Required feature "A" includes at least 2 of the following headache characteristics: unilateral location, pulsatile quality, moderate or severe pain intensity, or aggravation by or causing avoidance of routine physical activity. Required feature "B" includes at least 1 of the following during the headache: nausea and/or vomiting, or photophobia and phonophobia. Least Squares (LS) mean was calculated using mixed model repeated measures (MMRM) methodology with treatment, pooled investigative site, period, and treatment-by-period interaction, baseline and baseline-by-period interaction.
Outcome measures
| Measure |
Placebo
n=134 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=69 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Mean Change From Baseline in Number of Migraine Attacks in the Last 28-Day Period of the 12-Week Treatment Phase
|
-2.65 Migraine attacks
Standard Error 0.17
|
-2.98 Migraine attacks
Standard Error 0.23
|
-2.87 Migraine attacks
Standard Error 0.22
|
-3.46 Migraine attacks
Standard Error 0.23
|
-3.01 Migraine attacks
Standard Error 0.23
|
SECONDARY outcome
Timeframe: Week 12Population: All participants with a valid 28-day baseline assessment of migraine headache days who received at least 1 dose of study treatment and had evaluable postbaseline headache data during the time period of analysis.
The criteria for a migraine headache was adapted from the standard International Headache Society (IHS) International Classification of Headache Disorders (ICHD)-3 beta definition. The definition of a migraine headache was a headache with or without aura, of ≥30 minutes (min) duration, and with both ("A" and "B") required features from the IHS ICHD-3 beta definition. Required feature "A" includes at least 2 of the following headache characteristics: unilateral location, pulsatile quality, moderate or severe pain intensity, or aggravation by or causing avoidance of routine physical activity. Required feature "B" includes at least 1 of the following during the headache: nausea and/or vomiting, or photophobia and phonophobia.
Outcome measures
| Measure |
Placebo
n=134 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=69 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Percentage of Participants With ≥50% Reduction in Number of Migraine Headache Days in the Last 28-Day Period of the 12-Week Treatment Phase
|
60.9 Percentage of participants
|
75.4 Percentage of participants
|
65.5 Percentage of participants
|
76.5 Percentage of participants
|
70.1 Percentage of participants
|
SECONDARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All participants with a valid 28-day baseline assessment of migraine headache days who received at least 1 dose of study treatment and had evaluable postbaseline headache data.
A migraine attack was defined as beginning on any day a migraine headache day was recorded and ending when a migraine headache-free day occurred. The criteria was adapted from the standard IHS ICHD-3 beta definition. The definition of a migraine headache was a headache with or without aura, of ≥30 minutes (min) duration, and with both ("A" and "B") required features from the IHS ICHD-3 beta definition. Required feature "A" includes at least 2 of the following headache characteristics: unilateral location, pulsatile quality, moderate or severe pain intensity, or aggravation by or causing avoidance of routine physical activity. Required feature "B" includes at least 1 of the following during the headache: nausea and/or vomiting, or photophobia and phonophobia. Least Squares (LS) means was determined by mixed model repeated measures (MMRM) methodology with treatment, pooled investigative site, period, and treatment-by-period interaction, baseline and baseline-by-period interaction.
Outcome measures
| Measure |
Placebo
n=134 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=69 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Mean Change From Baseline in the Number of Days of Medication Use for the Treatment of Migraine Headache in the Last 28-Day Period of the 12-Week Treatment Phase
|
-2.51 Days
Standard Error 0.23
|
-3.27 Days
Standard Error 0.32
|
-2.58 Days
Standard Error 0.31
|
-3.59 Days
Standard Error 0.31
|
-3.15 Days
Standard Error 0.32
|
SECONDARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All participants with a valid 28-day baseline assessment of migraine headache days who received at least 1 dose of study treatment and had evaluable postbaseline headache data.
Number of headache hours calculated as the total number of headache hours in a 28-day period on which a headache occurred. Least Squares (LS) means was determined by mixed model repeated measures (MMRM) methodology with treatment, pooled investigative site, period, and treatment-by-period interaction, baseline and baseline-by-period interaction.
Outcome measures
| Measure |
Placebo
n=134 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=69 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Mean Change From Baseline in Number of Headache Hours in the Last 28-Day Period of the 12-Week Treatment Phase
|
-16.56 Hours
Standard Error 1.73
|
-20.15 Hours
Standard Error 2.45
|
-19.38 Hours
Standard Error 2.35
|
-22.29 Hours
Standard Error 2.39
|
-24.45 Hours
Standard Error 2.42
|
SECONDARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All randomized participants who received at least 1 dose of study drug and have non-missing values at baseline and post-baseline value.
MSQL consists of 14 questions across 3 dimensions (role function-restrictive, role function-preventive, and emotional function). All question values range from 1 to 6. Participants rated each item from 1 (none of the time) to 6 (all of the time). Since each item was presented as a negative statement, participant responses were recorded before item scores were calculated. Then, dimension scores were calculated as the sum of the recorded items for that specific dimension. Each dimension score was transformed into a score that ranged from 0 to 100. The transformation formula for the restrictive function = \[(dimension score-7)\*100\]/35, for the preventive function = \[(dimension score-4)\*100\]/20, and for the emotional function = \[(dimension score-3)\*100\]/15. A lower score indicated a poorer quality of life associated with that domain. LS means was determined by Analysis of covariance (ANCOVA) with treatment, pooled investigative site and baseline.
Outcome measures
| Measure |
Placebo
n=133 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=63 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=67 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=63 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=64 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Change From Baseline to 12 Week Endpoint in Migraine Specific Quality of Life (MSQL) Questionnaire Total Scores
|
21.08 units on a scale
Standard Error 1.82
|
27.53 units on a scale
Standard Error 2.53
|
25.35 units on a scale
Standard Error 2.46
|
30.23 units on a scale
Standard Error 2.58
|
27.49 units on a scale
Standard Error 2.51
|
SECONDARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All randomized participants who received at least 1 dose of study drug and have non-missing values at baseline and post-baseline value.
The HIT-6 consists of 6 questions to measure the impact of headaches on the participants ability to function on the job, at school, at home and in social situations. A score to each question will be assigned as follows: never - 6, rarely - 8, sometimes - 10, very often - 11, and always - 13. The composite score is calculated as the sum of the scores for all 6 questions, the total score ranges between 36 and 78 with higher total scores reflecting more severe impact of headaches. LS means was determined by ANCOVA with treatment, pooled investigative site and baseline.
Outcome measures
| Measure |
Placebo
n=133 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=63 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=67 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=63 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=64 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Change From Baseline to 12 Week Endpoint in the Headache Impact Test-6™ (HIT-6™) Scores
|
-7.26 units on a scale
Standard Error 0.79
|
-9.26 units on a scale
Standard Error 1.09
|
-8.46 units on a scale
Standard Error 1.06
|
-9.95 units on a scale
Standard Error 1.12
|
-8.27 units on a scale
Standard Error 1.09
|
SECONDARY outcome
Timeframe: 12 WeeksPopulation: All randomized participants who received at least 1 dose of study drug with non-missing baseline and postbaseline measures for serum concentration of galcanezumab.
Blood serum concentrations of galcanezumab.
Outcome measures
| Measure |
Placebo
n=59 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=66 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=62 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=63 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Serum Concentration of Galcanezumab
|
840 nanomoles per litre (nmol/L)
Standard Deviation 602
|
4650 nanomoles per litre (nmol/L)
Standard Deviation 2430
|
13200 nanomoles per litre (nmol/L)
Standard Deviation 7060
|
32100 nanomoles per litre (nmol/L)
Standard Deviation 19100
|
—
|
SECONDARY outcome
Timeframe: 12 WeeksPopulation: All randomized participants who received at least 1 dose of study drug with non-missing baseline and postbaseline measures for CGRP plasma concentration.
CGRP has been shown to be involved in the pathophysiology of migraine through dilation of cerebral and dural blood vessels, release of inflammatory mediators, and transmission of nociceptive (pain) information from intracranial blood vessels to the nervous system (Villalón and Olesen 2009). In migraineurs, serum concentrations of CGRP are significantly elevated during migraine attacks (Goadsby et al. 1990; Goadsby and Edvinsson 1993).
Outcome measures
| Measure |
Placebo
n=14 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=55 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=63 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=61 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=63 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Plasma Concentration of Calcitonin Gene-Related Peptide (CGRP)
|
0.1810 nanomoles per litre (nmol/L)
Standard Deviation 0.1030
|
0.4750 nanomoles per litre (nmol/L)
Standard Deviation 0.3940
|
1.5700 nanomoles per litre (nmol/L)
Standard Deviation 0.7010
|
2.8000 nanomoles per litre (nmol/L)
Standard Deviation 1.2200
|
3.8300 nanomoles per litre (nmol/L)
Standard Deviation 1.3100
|
SECONDARY outcome
Timeframe: Baseline through 12 WeeksPopulation: All randomized participants who received at least 1 dose of study drug with non-missing baseline and postbaseline ADA measures.
The percent of participants with treatment emergent Anti-drug Antibodies (ADA) were assessed at week 1 to 12. A participant was considered to have treatment-emergent Galcanezumab ADA if the participant had at least 1 titer that was treatment-emergent relative to baseline, defined as any of the following: A negative baseline ADA result and a subsequent positive post-baseline ADA result with a titer \>=20; or a positive ADA results and a subsequent positive post-baseline ADA results with a 4-fold or greater increase in titer from the baseline measurement.
Outcome measures
| Measure |
Placebo
n=136 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=66 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=68 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=65 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Percentage of Participants Developing Anti-drug Antibodies to Galcanezumab
|
2.2 Percentage of participants
|
7.7 Percentage of participants
|
4.6 Percentage of participants
|
2.9 Percentage of participants
|
3.1 Percentage of participants
|
SECONDARY outcome
Timeframe: Baseline through Week 12Population: All randomized participants who received at least 1 dose of study drug and with non-missing baseline and postbaseline C-SSRS assessment.
The C-SSRS captures the occurrence, severity, and frequency of suicide-related thoughts and behaviors during the assessment period. The scale includes suggested questions to solicit the type of information needed to determine if a suicide-related thought or behavior occurred. Some questions are binary responses (yes/no) and some are on a scale of 1 (low severity) to 5 (high severity). Suicidal behavior: a "yes" answer to any of 5 suicidal behavior questions: preparatory acts or behavior, aborted attempt, interrupted attempt, actual attempt, and completed suicide.
Outcome measures
| Measure |
Placebo
n=136 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=66 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=67 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=68 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Percentage of Participants With Suicidal Ideation and Behaviors Assessed by the Columbia Suicide Severity Rating Scale (C-SSRS) Scores
Suicidal Ideation
|
0 Percentage of Participants
|
0 Percentage of Participants
|
0 Percentage of Participants
|
0 Percentage of Participants
|
1.52 Percentage of Participants
|
|
Percentage of Participants With Suicidal Ideation and Behaviors Assessed by the Columbia Suicide Severity Rating Scale (C-SSRS) Scores
Suicidal Behavior
|
0 Percentage of Participants
|
0 Percentage of Participants
|
0 Percentage of Participants
|
0 Percentage of Participants
|
0 Percentage of Participants
|
SECONDARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All randomized participants with a valid 28-day baseline assessment of migraine headache days who received at least 1 dose of study treatment and had evaluable postbaseline headache data.
Number of calendar days on which a headache lasts ≥4 hours which includes migraines, probable migraines (PM) and nonmigraines. Criteria for migraine headache (MH) was adapted from standard IHS ICHD-3 beta definition. It is defined as headache with or without aura, of ≥30 min duration, and with both ("A" and "B") required features from IHS ICHD-3 beta definition. Required feature "A" includes ≥2 of following headache characteristics: unilateral location, pulsatile quality, moderate or severe pain intensity, or aggravation by or causing avoidance of routine physical activity. Required feature "B" includes at least 1 of following during headache: nausea and/or vomiting, or photophobia and phonophobia. PM is headache with or without aura, but missing 1 feature needed to fulfill all criteria for MH. LS means were calculated using MMRM with treatment, pooled investigative site, period, and treatment-by-period interaction, baseline and baseline-by-period interaction.
Outcome measures
| Measure |
Placebo
n=134 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=69 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Mean Change From Baseline in the Number of Headache Days in the Last 28-Day Period of the 12-Week Treatment Phase
|
-2.47 Days
Standard Error 0.22
|
-2.81 Days
Standard Error 0.32
|
-2.57 Days
Standard Error 0.30
|
-3.11 Days
Standard Error 0.31
|
-3.37 Days
Standard Error 0.31
|
SECONDARY outcome
Timeframe: Baseline, 12 WeeksPopulation: All participants with a valid 28-day baseline assessment of migraine headache days who received at least 1 dose of study treatment and had evaluable postbaseline headache data.
Number of calendar days on which headache lasts ≥4 hrs it includes migraines, PM \& non-migraines. MH is headache with or without aura, of ≥30 min duration, and with both ("A" and "B") required features from IHS ICHD-3 beta definition. Required feature "A" includes ≥2 of following headache characteristics: unilateral location, pulsatile quality, moderate or severe pain intensity, or aggravation by or causing avoidance of routine physical activity. Required feature "B" includes at least 1 of following during headache: nausea \&/or vomiting, or photophobia \& phonophobia. PM is headache with or without aura, but missing 1 feature needed to fulfill all criteria for MH. Severity was measured via interactive voice response system questionnaire "What was the worst headache pain? For mild press 1. For moderate 2. For severe press 3". LSmean was calculated using MMRM with treatment, pooled investigative site, period, treatment-by-period interaction, baseline and baseline-by-period interaction.
Outcome measures
| Measure |
Placebo
n=134 Participants
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab
n=65 Participants
5mg of galcanezumab given as subcutaneous (SQ) injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab
n=68 Participants
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab
n=69 Participants
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab
n=66 Participants
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|
|
Mean Change From Baseline in the Number of Moderate-Severe Headache Days in the Last 28-Day Period of the 12-Week Treatment Phase
|
-2.33 Days
Standard Error 0.20
|
-2.49 Days
Standard Error 0.28
|
-2.33 Days
Standard Error 0.27
|
-2.88 Days
Standard Error 0.28
|
-3.13 Days
Standard Error 0.28
|
Adverse Events
Placebo - Treatment Phase
5mg Galcanezumab-Treatment Phase
50mg Galcanezumab-Treatment Phase
120mg Galcanezumab-Treatment Phase
300mg Galcanezumab-Treatment Phase
Placebo - Post-Treatment Phase
5mg Galcanezumab-Post-Treatment Phase
50mg Galcanezumab-Post-Treatment Phase
120mg Galcanezumab-Post-Treatment Phase
300mg Galcanezumab-Post-Treatment Phase
Serious adverse events
| Measure |
Placebo - Treatment Phase
n=137 participants at risk
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab-Treatment Phase
n=68 participants at risk
5mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab-Treatment Phase
n=68 participants at risk
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab-Treatment Phase
n=70 participants at risk
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab-Treatment Phase
n=67 participants at risk
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
Placebo - Post-Treatment Phase
n=125 participants at risk
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab-Post-Treatment Phase
n=61 participants at risk
5mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab-Post-Treatment Phase
n=66 participants at risk
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab-Post-Treatment Phase
n=63 participants at risk
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab-Post-Treatment Phase
n=65 participants at risk
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Gastrointestinal disorders
Crohn's disease
|
0.00%
0/137 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
0.00%
0/70 • Up To 24 Weeks
|
0.00%
0/67 • Up To 24 Weeks
|
0.00%
0/125 • Up To 24 Weeks
|
1.6%
1/61 • Number of events 1 • Up To 24 Weeks
|
0.00%
0/66 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
0.00%
0/65 • Up To 24 Weeks
|
|
Infections and infestations
Appendicitis
|
0.00%
0/137 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
1.4%
1/70 • Number of events 1 • Up To 24 Weeks
|
0.00%
0/67 • Up To 24 Weeks
|
0.00%
0/125 • Up To 24 Weeks
|
0.00%
0/61 • Up To 24 Weeks
|
0.00%
0/66 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
0.00%
0/65 • Up To 24 Weeks
|
|
Psychiatric disorders
Suicidal Ideation
|
0.00%
0/137 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
0.00%
0/70 • Up To 24 Weeks
|
0.00%
0/67 • Up To 24 Weeks
|
0.00%
0/125 • Up To 24 Weeks
|
0.00%
0/61 • Up To 24 Weeks
|
0.00%
0/66 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
1.5%
1/65 • Number of events 1 • Up To 24 Weeks
|
|
Congenital, familial and genetic disorders
Ankyloglossia Congenital
|
0.00%
0/137 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
0.00%
0/68 • Up To 24 Weeks
|
0.00%
0/70 • Up To 24 Weeks
|
1.5%
1/67 • Number of events 1 • Up To 24 Weeks
|
0.00%
0/125 • Up To 24 Weeks
|
0.00%
0/61 • Up To 24 Weeks
|
0.00%
0/66 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
0.00%
0/65 • Up To 24 Weeks
|
Other adverse events
| Measure |
Placebo - Treatment Phase
n=137 participants at risk
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab-Treatment Phase
n=68 participants at risk
5mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab-Treatment Phase
n=68 participants at risk
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab-Treatment Phase
n=70 participants at risk
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab-Treatment Phase
n=67 participants at risk
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
Placebo - Post-Treatment Phase
n=125 participants at risk
Placebo given as SQ injections once every 28 days during a 12 week treatment period.
|
5mg Galcanezumab-Post-Treatment Phase
n=61 participants at risk
5mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
50mg Galcanezumab-Post-Treatment Phase
n=66 participants at risk
50mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
120mg Galcanezumab-Post-Treatment Phase
n=63 participants at risk
120mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
300mg Galcanezumab-Post-Treatment Phase
n=65 participants at risk
300mg of galcanezumab given as SQ injections once every 28 days during a 12 week treatment period.
|
|---|---|---|---|---|---|---|---|---|---|---|
|
Gastrointestinal disorders
Nausea
|
2.9%
4/137 • Number of events 4 • Up To 24 Weeks
|
1.5%
1/68 • Number of events 2 • Up To 24 Weeks
|
2.9%
2/68 • Number of events 2 • Up To 24 Weeks
|
0.00%
0/70 • Up To 24 Weeks
|
6.0%
4/67 • Number of events 5 • Up To 24 Weeks
|
0.00%
0/125 • Up To 24 Weeks
|
1.6%
1/61 • Number of events 1 • Up To 24 Weeks
|
0.00%
0/66 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
0.00%
0/65 • Up To 24 Weeks
|
|
General disorders
Injection site pain
|
2.9%
4/137 • Number of events 6 • Up To 24 Weeks
|
10.3%
7/68 • Number of events 11 • Up To 24 Weeks
|
8.8%
6/68 • Number of events 15 • Up To 24 Weeks
|
14.3%
10/70 • Number of events 13 • Up To 24 Weeks
|
13.4%
9/67 • Number of events 18 • Up To 24 Weeks
|
0.00%
0/125 • Up To 24 Weeks
|
0.00%
0/61 • Up To 24 Weeks
|
0.00%
0/66 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
0.00%
0/65 • Up To 24 Weeks
|
|
Infections and infestations
Nasopharyngitis
|
2.2%
3/137 • Number of events 3 • Up To 24 Weeks
|
11.8%
8/68 • Number of events 8 • Up To 24 Weeks
|
4.4%
3/68 • Number of events 3 • Up To 24 Weeks
|
8.6%
6/70 • Number of events 6 • Up To 24 Weeks
|
3.0%
2/67 • Number of events 2 • Up To 24 Weeks
|
0.80%
1/125 • Number of events 1 • Up To 24 Weeks
|
1.6%
1/61 • Number of events 1 • Up To 24 Weeks
|
1.5%
1/66 • Number of events 1 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
0.00%
0/65 • Up To 24 Weeks
|
|
Infections and infestations
Upper respiratory tract infection
|
8.8%
12/137 • Number of events 15 • Up To 24 Weeks
|
10.3%
7/68 • Number of events 7 • Up To 24 Weeks
|
11.8%
8/68 • Number of events 8 • Up To 24 Weeks
|
11.4%
8/70 • Number of events 8 • Up To 24 Weeks
|
6.0%
4/67 • Number of events 4 • Up To 24 Weeks
|
3.2%
4/125 • Number of events 4 • Up To 24 Weeks
|
0.00%
0/61 • Up To 24 Weeks
|
1.5%
1/66 • Number of events 1 • Up To 24 Weeks
|
3.2%
2/63 • Number of events 2 • Up To 24 Weeks
|
3.1%
2/65 • Number of events 3 • Up To 24 Weeks
|
|
Reproductive system and breast disorders
Dysmenorrhoea
|
0.00%
0/137 • Up To 24 Weeks
|
1.5%
1/68 • Number of events 4 • Up To 24 Weeks
|
5.9%
4/68 • Number of events 4 • Up To 24 Weeks
|
0.00%
0/70 • Up To 24 Weeks
|
3.0%
2/67 • Number of events 2 • Up To 24 Weeks
|
0.80%
1/125 • Number of events 1 • Up To 24 Weeks
|
0.00%
0/61 • Up To 24 Weeks
|
0.00%
0/66 • Up To 24 Weeks
|
0.00%
0/63 • Up To 24 Weeks
|
1.5%
1/65 • Number of events 2 • Up To 24 Weeks
|
Additional Information
Chief Medical Officer
Eli Lilly and Company
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place
Restriction type: GT60