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.

Recruitment status

COMPLETED

Study phase

PHASE2

Target enrollment

414 participants

Primary outcome timeframe

Baseline, 12 Weeks

Results posted on

2018-11-23

Participant Flow

Treatment period (0 to 12 weeks), Post-treatment period (12 to 24 weeks)

Participant milestones

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

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

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 Weeks

Population: 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

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 Weeks

Population: 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

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 12

Population: 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

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 Weeks

Population: 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

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 Weeks

Population: 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

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 Weeks

Population: 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

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 Weeks

Population: 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

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 Weeks

Population: 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

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 Weeks

Population: 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

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 Weeks

Population: 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

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 12

Population: 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

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 Weeks

Population: 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

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 Weeks

Population: 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

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

Serious events: 0 serious events
Other events: 23 other events
Deaths: 0 deaths

5mg Galcanezumab-Treatment Phase

Serious events: 0 serious events
Other events: 20 other events
Deaths: 0 deaths

50mg Galcanezumab-Treatment Phase

Serious events: 0 serious events
Other events: 18 other events
Deaths: 0 deaths

120mg Galcanezumab-Treatment Phase

Serious events: 1 serious events
Other events: 23 other events
Deaths: 0 deaths

300mg Galcanezumab-Treatment Phase

Serious events: 1 serious events
Other events: 19 other events
Deaths: 0 deaths

Placebo - Post-Treatment Phase

Serious events: 0 serious events
Other events: 6 other events
Deaths: 0 deaths

5mg Galcanezumab-Post-Treatment Phase

Serious events: 1 serious events
Other events: 2 other events
Deaths: 0 deaths

50mg Galcanezumab-Post-Treatment Phase

Serious events: 0 serious events
Other events: 2 other events
Deaths: 0 deaths

120mg Galcanezumab-Post-Treatment Phase

Serious events: 0 serious events
Other events: 2 other events
Deaths: 0 deaths

300mg Galcanezumab-Post-Treatment Phase

Serious events: 1 serious events
Other events: 3 other events
Deaths: 0 deaths

Serious adverse events

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

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

Phone: 800-545-5979

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place

Restriction type: GT60