Trial Outcomes & Findings for Study of Oral Atogepant Tablets to Assess Change in Disease Activity in Adult Japanese Participants With Episodic Migraine (NCT NCT05861427)

NCT ID: NCT05861427

Last Updated: 2026-06-11

Results Overview

Participants recorded daily duration of migraine in an eDiary. A migraine day was any calendar day on which the participant experienced a migraine headache qualified by duration or acute symptomatic medication use. The monthly (4-week) migraine days was defined as the total number of reported migraine days in eDiary divided by total number of days with eDiary records during each 4-week period and multiplied by 28. Each 4-week period was averaged. Baseline was defined as the number of migraine days during the last 28 days of the Baseline phase, from Day -28 to -1. Negative change from Baseline indicates improvement. A Mixed-effects Model for Repeated Measure (MMRM) was used for analysis.

Recruitment status

COMPLETED

Study phase

PHASE3

Target enrollment

524 participants

Primary outcome timeframe

Up to Week 12

Results posted on

2026-06-11

Participant Flow

Participant milestones

Participant milestones
Measure
Placebo
Participants who were randomized to placebo QD for Weeks 1-12.
Placebo/Atogepant 10 mg
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 10 mg QD for Weeks 12-24.
Placebo/Atogepant 30 mg
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 30 mg QD for Weeks 12-24.
Placebo/Atogepant 60 mg
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 60 mg QD for Weeks 12-24.
Atogepant 10 mg
Participants who were randomized to atogepant 10 mg once daily (QD) for Weeks 1-24.
Atogepant 30 mg
Participants who were randomized to atogepant 30 mg once daily (QD) for Weeks 1-24.
Atogepant 60 mg
Participants who were randomized to atogepant 60 mg once daily (QD) for Weeks 1-24.
Double-Blind Treatment (Wks 1-12)
STARTED
134
0
0
0
127
131
132
Double-Blind Treatment (Wks 1-12)
Never Received Any Study Treatment
0
0
0
0
0
0
1
Double-Blind Treatment (Wks 1-12)
Received Randomized Study Treatment
133
0
0
0
126
131
131
Double-Blind Treatment (Wks 1-12)
Received Study Treatment Other Than Randomized
1
0
0
0
1
0
0
Double-Blind Treatment (Wks 1-12)
COMPLETED
131
0
0
0
124
126
130
Double-Blind Treatment (Wks 1-12)
NOT COMPLETED
3
0
0
0
3
5
2
Active Treatment Extension (Wks 12-24)
STARTED
0
46
43
42
124
126
130
Active Treatment Extension (Wks 12-24)
COMPLETED
0
45
43
41
121
125
126
Active Treatment Extension (Wks 12-24)
NOT COMPLETED
0
1
0
1
3
1
4

Reasons for withdrawal

Reasons for withdrawal
Measure
Placebo
Participants who were randomized to placebo QD for Weeks 1-12.
Placebo/Atogepant 10 mg
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 10 mg QD for Weeks 12-24.
Placebo/Atogepant 30 mg
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 30 mg QD for Weeks 12-24.
Placebo/Atogepant 60 mg
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 60 mg QD for Weeks 12-24.
Atogepant 10 mg
Participants who were randomized to atogepant 10 mg once daily (QD) for Weeks 1-24.
Atogepant 30 mg
Participants who were randomized to atogepant 30 mg once daily (QD) for Weeks 1-24.
Atogepant 60 mg
Participants who were randomized to atogepant 60 mg once daily (QD) for Weeks 1-24.
Double-Blind Treatment (Wks 1-12)
Lost to Follow-up
1
0
0
0
0
0
0
Double-Blind Treatment (Wks 1-12)
Withdrawal by Subject
1
0
0
0
1
2
1
Double-Blind Treatment (Wks 1-12)
Not disclosed
1
0
0
0
2
3
1
Active Treatment Extension (Wks 12-24)
Lost to Follow-up
0
0
0
0
0
0
1
Active Treatment Extension (Wks 12-24)
Withdrawal by Subject
0
1
0
0
2
0
2
Active Treatment Extension (Wks 12-24)
Not Disclosed
0
0
0
1
1
1
1

Baseline Characteristics

Study of Oral Atogepant Tablets to Assess Change in Disease Activity in Adult Japanese Participants With Episodic Migraine

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Placebo
n=134 Participants
Participants who received placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=126 Participants
Participants who received atogepant 10 mg once daily (QD) for 24 weeks.
Atogepant 30 mg
n=131 Participants
Participants who received atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=132 Participants
Participants who received atogepant 60 mg once daily (QD) for 24 weeks.
Total
n=523 Participants
Total of all reporting groups
Age, Continuous
44.8 years
STANDARD_DEVIATION 10.54 • n=20 Participants
41.3 years
STANDARD_DEVIATION 11.71 • n=20 Participants
43.2 years
STANDARD_DEVIATION 11.40 • n=40 Participants
42.5 years
STANDARD_DEVIATION 10.25 • n=6 Participants
43.0 years
STANDARD_DEVIATION 11.02 • n=7 Participants
Sex: Female, Male
Female
117 Participants
n=20 Participants
106 Participants
n=20 Participants
104 Participants
n=40 Participants
110 Participants
n=6 Participants
437 Participants
n=7 Participants
Sex: Female, Male
Male
17 Participants
n=20 Participants
20 Participants
n=20 Participants
27 Participants
n=40 Participants
22 Participants
n=6 Participants
86 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
134 Participants
n=20 Participants
126 Participants
n=20 Participants
131 Participants
n=40 Participants
132 Participants
n=6 Participants
523 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Asian
134 Participants
n=20 Participants
126 Participants
n=20 Participants
131 Participants
n=40 Participants
132 Participants
n=6 Participants
523 Participants
n=7 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Black or African American
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
White
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=20 Participants
0 Participants
n=20 Participants
0 Participants
n=40 Participants
0 Participants
n=6 Participants
0 Participants
n=7 Participants

PRIMARY outcome

Timeframe: Up to Week 12

Population: Modified Intent-to-Treat Population (mITT)

Participants recorded daily duration of migraine in an eDiary. A migraine day was any calendar day on which the participant experienced a migraine headache qualified by duration or acute symptomatic medication use. The monthly (4-week) migraine days was defined as the total number of reported migraine days in eDiary divided by total number of days with eDiary records during each 4-week period and multiplied by 28. Each 4-week period was averaged. Baseline was defined as the number of migraine days during the last 28 days of the Baseline phase, from Day -28 to -1. Negative change from Baseline indicates improvement. A Mixed-effects Model for Repeated Measure (MMRM) was used for analysis.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=130 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=131 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=133 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=127 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Change From Baseline in Mean Monthly Migraine Days
-3.14 migraine days per month
Interval -3.63 to -2.64
-3.34 migraine days per month
Interval -3.83 to -2.85
-1.24 migraine days per month
Interval -1.72 to -0.75
-2.80 migraine days per month
Interval -3.3 to -2.3

PRIMARY outcome

Timeframe: Up to Week 12

Population: Safety Population 1 (Double-Blind Treatment Period)

An adverse event (AE) is defined as any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=131 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=132 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=134 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=126 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Number of Participants Experiencing With Adverse Events (AEs)
51 Participants
57 Participants
62 Participants
57 Participants

SECONDARY outcome

Timeframe: Up to Week 12

Population: mITT Population

Participants recorded daily total duration of a headache in an eDiary. A headache day is any calendar day on which the participant experienced a headache qualified by duration or acute symptomatic medication use. The monthly (4-week) headache days were defined as the total number of reported headache days in the eDiary divided by the total number of days with eDiary records during each 4-week period and multiplied by 28. Each 4-week period was averaged. Baseline was defined as the number of migraine days during the last 28 days of the Baseline phase, from Day -28 to -1. Negative change from Baseline indicates improvement. MMRM was used for analysis.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=130 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=131 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=133 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=127 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Change From Baseline in Mean Monthly Headache Days
-3.31 headache days per month
Standard Error 0.274
-3.50 headache days per month
Standard Error 0.275
-1.01 headache days per month
Standard Error 0.269
-3.17 headache days per month
Standard Error 0.277

SECONDARY outcome

Timeframe: Up to Week 12

Population: mITT Population

Participants recorded allowed medication(s) to treat an acute migraine in the daily eDiary. The monthly (4-week) acute medication use days was defined as the total number of reported acute medication use days in the eDiary divided by the total number of days with eDiary records during each 4-week period and multiplied by 28. Each 4-week period was averaged. Baseline was defined as the number of acute medication use days during the last 28 days of the Baseline phase, from Day -28 to -1. A negative change from Baseline indicates improvement. MMRM was used for the analysis.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=130 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=131 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=133 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=127 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Change From Baseline in Mean Monthly Acute Medication Use Days
-2.55 acute medication use days per month
Standard Error 0.250
-2.69 acute medication use days per month
Standard Error 0.250
-0.22 acute medication use days per month
Standard Error 0.246
-2.34 acute medication use days per month
Standard Error 0.254

SECONDARY outcome

Timeframe: Up to Week 12

Population: mITT Population

Participants recorded daily duration of migraine in an eDiary. A migraine day was any calendar day on which the participant experienced a migraine headache qualified by duration or acute symptomatic medication use. The monthly (4-week) migraine days is equal to total number of reported migraine days in eDiary divided by total number of days with eDiary records in each 4-week period multiplied by 28. Each 4-week period was averaged.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=130 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=131 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=133 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=127 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Percentage of Participants Achieving At Least 50% Reduction in the 3-month Average of Monthly Migraine Days
42.3 percentage of participants
50.4 percentage of participants
15.0 percentage of participants
40.9 percentage of participants

SECONDARY outcome

Timeframe: Up to Week 12

Population: mITT Population

MSQ v2.1 is a 14-item questionnaire designed to measure health-related quality-of-life impairments attributed to migraine in the past 4 weeks. It is divided into three domains: role function-restrictive (questions 1-7, score range 7 to 42) assesses how migraines limit one's daily social and work-related activities; role function-preventive (questions 8-11, score ranges 4 to 24) assesses how migraines prevent these activities; and the emotional function (questions 12-14, score ranges 3 to 18) domain assesses the emotions associated with migraines. Participants respond to items using a 6-point scale where 1=none of the time and 6=all of the time. Raw dimension scores are computed as a sum of item responses and rescaled to a 0 to 100 scale, where higher scores from Baseline indicate better quality of life. MMRM was used for the analysis.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=128 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=130 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=132 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=124 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Change From Baseline in Migraine Specific Quality of Life Questionnaire, Version 2.1 (MSQ v2.1) Role Function-Restrictive Domain Score
17.19 score on a scale
Standard Error 1.250
17.55 score on a scale
Standard Error 1.245
8.33 score on a scale
Standard Error 1.229
15.39 score on a scale
Standard Error 1.265

SECONDARY outcome

Timeframe: Up to Week 12

Population: mITT Population

The AIM-D is an 11-item daily diary measure that assesses the impact of migraine and is comprised of two domains that evaluate performance of daily activities (7 items) and physical impairment (4 items). Participants are asked to rate the level of difficulty experienced in the past 24 hours with performance of daily activities and physical impairment using a 6 point rating scale ranging from "Not difficult at all" to "I could not do it at all." Scores range from 0-100 scale, with higher scores indicating greater impact of migraine.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=130 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=129 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=133 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=126 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Change From Baseline in Mean Monthly Performance of Daily Activities Domain Score of the Activity Impairment in Migraine - Diary (AIM-D)
-5.31 score on a scale
Standard Error 0.364
-4.90 score on a scale
Standard Error 0.367
-2.35 score on a scale
Standard Error 0.357
-4.73 score on a scale
Standard Error 0.369

SECONDARY outcome

Timeframe: Up to Week 12

Population: mITT Population

The AIM-D is an 11-item daily diary measure that assesses the impact of migraine and is comprised of two domains that evaluate performance of daily activities (7 items) and physical impairment (4 items). Participants are asked to rate the level of difficulty experienced in the past 24 hours with performance of daily activities and physical impairment using a 6 point rating scale ranging from "Not difficult at all" to "I could not do it at all." Scores range from 0-100 scale, with higher scores indicating greater impact of migraine.

Outcome measures

Outcome measures
Measure
Atogepant 30 mg
n=130 Participants
Participants who were randomized to atogepant 30 mg once daily (QD) for 24 weeks.
Atogepant 60 mg
n=129 Participants
Participants who were randomized to atogepant 60 mg once daily (QD) for 24 weeks.
Placebo
n=133 Participants
Participants who were randomized to placebo QD for 12 weeks. Participants were re-randomized at Week 12 to receive atogepant 10 mg, 30 mg or 60 mg QD for 12 weeks.
Atogepant 10 mg
n=126 Participants
Participants who were randomized to atogepant 10 mg once daily (QD) for 24 weeks.
Change From Baseline in Mean Monthly Physical Impairment Domain Score of the AIM-D
-4.89 score on a scale
Standard Error 0.357
-4.49 score on a scale
Standard Error 0.360
-2.12 score on a scale
Standard Error 0.351
-4.32 score on a scale
Standard Error 0.363

Adverse Events

Atogepant 60 mg

Serious events: 0 serious events
Other events: 40 other events
Deaths: 0 deaths

Placebo

Serious events: 1 serious events
Other events: 38 other events
Deaths: 0 deaths

Placebo/Atogepant 10 mg

Serious events: 1 serious events
Other events: 18 other events
Deaths: 0 deaths

Placebo/Atogepant 30 mg

Serious events: 0 serious events
Other events: 15 other events
Deaths: 0 deaths

Atogepant 30 mg

Serious events: 1 serious events
Other events: 40 other events
Deaths: 0 deaths

Placebo/Atogepant 60 mg

Serious events: 0 serious events
Other events: 12 other events
Deaths: 0 deaths

Atogepant 10 mg

Serious events: 2 serious events
Other events: 39 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
Atogepant 60 mg
n=132 participants at risk
Participants who were randomized to atogepant 60 mg once daily (QD) for Weeks 1-24.
Placebo
n=134 participants at risk
Participants who were randomized to placebo QD for Weeks 1-12.
Placebo/Atogepant 10 mg
n=46 participants at risk
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 10 mg QD for Weeks 12-24.
Placebo/Atogepant 30 mg
n=44 participants at risk
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 30 mg QD for Weeks 12-24.
Atogepant 30 mg
n=131 participants at risk
Participants who were randomized to atogepant 30 mg once daily (QD) for Weeks 1-24.
Placebo/Atogepant 60 mg
n=41 participants at risk
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 60 mg QD for Weeks 12-24.
Atogepant 10 mg
n=126 participants at risk
Participants who were randomized to atogepant 10 mg once daily (QD) for Weeks 1-24.
Blood and lymphatic system disorders
ANAEMIA
0.00%
0/132 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/134 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/46 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/44 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.76%
1/131 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/41 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/126 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Cardiac disorders
PRINZMETAL ANGINA
0.00%
0/132 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/134 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/46 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/44 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/131 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/41 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.79%
1/126 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Gastrointestinal disorders
HAEMORRHOIDS
0.00%
0/132 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.75%
1/134 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
2.2%
1/46 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/44 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/131 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/41 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/126 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
OROPHARYNGEAL CANCER
0.00%
0/132 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/134 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/46 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/44 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/131 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/41 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.79%
1/126 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).

Other adverse events

Other adverse events
Measure
Atogepant 60 mg
n=132 participants at risk
Participants who were randomized to atogepant 60 mg once daily (QD) for Weeks 1-24.
Placebo
n=134 participants at risk
Participants who were randomized to placebo QD for Weeks 1-12.
Placebo/Atogepant 10 mg
n=46 participants at risk
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 10 mg QD for Weeks 12-24.
Placebo/Atogepant 30 mg
n=44 participants at risk
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 30 mg QD for Weeks 12-24.
Atogepant 30 mg
n=131 participants at risk
Participants who were randomized to atogepant 30 mg once daily (QD) for Weeks 1-24.
Placebo/Atogepant 60 mg
n=41 participants at risk
Participants who were randomized to placebo QD for 12 weeks, then re-randomized to receive atogepant 60 mg QD for Weeks 12-24.
Atogepant 10 mg
n=126 participants at risk
Participants who were randomized to atogepant 10 mg once daily (QD) for Weeks 1-24.
Gastrointestinal disorders
ABDOMINAL PAIN UPPER
3.8%
5/132 • Number of events 5 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/134 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
6.5%
3/46 • Number of events 3 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/44 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
3.8%
5/131 • Number of events 5 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
2.4%
1/41 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
2.4%
3/126 • Number of events 4 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Gastrointestinal disorders
CONSTIPATION
11.4%
15/132 • Number of events 15 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
9.0%
12/134 • Number of events 12 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
15.2%
7/46 • Number of events 7 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
4.5%
2/44 • Number of events 2 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
9.9%
13/131 • Number of events 13 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
7.3%
3/41 • Number of events 3 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
4.8%
6/126 • Number of events 6 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Gastrointestinal disorders
GASTRITIS
0.76%
1/132 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/134 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
2.2%
1/46 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/44 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.76%
1/131 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
2.4%
1/41 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.79%
1/126 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
General disorders
PYREXIA
1.5%
2/132 • Number of events 3 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/134 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
4.3%
2/46 • Number of events 2 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
2.3%
1/44 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/131 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
2.4%
1/41 • Number of events 1 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
3.2%
4/126 • Number of events 4 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Infections and infestations
COVID-19
5.3%
7/132 • Number of events 7 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
3.7%
5/134 • Number of events 5 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
4.3%
2/46 • Number of events 2 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
6.8%
3/44 • Number of events 3 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
3.1%
4/131 • Number of events 4 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/41 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
7.1%
9/126 • Number of events 9 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Infections and infestations
NASOPHARYNGITIS
14.4%
19/132 • Number of events 30 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
20.1%
27/134 • Number of events 29 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
15.2%
7/46 • Number of events 7 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
25.0%
11/44 • Number of events 13 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
17.6%
23/131 • Number of events 30 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
22.0%
9/41 • Number of events 9 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
16.7%
21/126 • Number of events 22 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
Reproductive system and breast disorders
VAGINAL HAEMORRHAGE
0.00%
0/132 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/134 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/46 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/44 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/131 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/41 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).
0.00%
0/126 • All-cause mortality & AE tables include events reported from time of informed consent to end of study. Median time on follow-up was 200, 200.5, 200, 200, 200, 201 & 200 days for Pbo, Pbo/10mg, Pbo/30mg, Pbo/60mg, Atogepant 10mg, 30mg & 60mg, respectively. One subject randomized to 60mg never recd study treatment (included in ITT 60mg but not in SP1); one subject randomized to 10mg took 60mg; one subject randomized to placebo then re-randomized to 60mg at Wk 12 recd 30mg from Wk 12-24.
All-cause mortality table is based on the ITT population. The ITT subjects were included in the analysis according to the treatment group to which they were randomized. The SAEs and Other tables are based on Safety Population 1 (includes all subjects who received at least 1 dose of study drug during the double-blind treatment period), and subjects were included in the analysis according to the actual treatment received (rather than as randomized).

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