Trial Outcomes & Findings for A 12-Week Placebo-Controlled Study to Investigate the Efficacy, Safety, and Tolerability of RO7017773 in Participants Aged 15-45 Years With Autism Spectrum Disorder (ASD) (NCT NCT04299464)

NCT ID: NCT04299464

Last Updated: 2025-01-28

Results Overview

Vineland-3 is a semi-structured interview that measures an individual's adaptive behavior across 3 domains: Communication, Socialization, and Daily Living skills. Each domain is composed of 3 subdomains. Subdomain raw score is based on item responses (3-point scale: 0=never present; 1=sometimes present; 2=usually present) and is calculated for each subdomain of the three main domains as the sum of the scores for each item within the subdomain. Raw scores of the 9 subdomains are used to derive Growth Scale Values (GSVs; range = 10-197). A conversion table for mapping raw scores to GSV scores is found in Appendix 3, Table B.2 in the Vineland-3 manual (Sparrow et al. 2016). GSV is a person-ability score used to track an individual's progress. Vineland-3 ABC Composite GSV score is calculated as the mean GSV score (summing the 9 GSV subdomain scores and dividing by 9; Vineland-3 ABC Composite GSV scores can range from 10-154). A higher score indicates better adaptive functioning.

Recruitment status

COMPLETED

Study phase

PHASE2

Target enrollment

104 participants

Primary outcome timeframe

Baseline to Week 12

Results posted on

2025-01-28

Participant Flow

Participants took part in the study across 26 investigative sites in 4 countries (United States, Canada, Spain, and Italy) from 31 March 2021 to 15 May 2024.

A total of 104 participants diagnosed with autism spectrum disorder (ASD) were randomized in 1:1:1 ratio to receive alogabat 20 mg, 60 mg and placebo.

Participant milestones

Participant milestones
Measure
Placebo
Participants received alogabat matching placebo, orally, once daily (QD) up to 12 weeks during the treatment period.
Alogabat 20 mg
Participants received alogabat, 20 milligrams (mg), orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Overall Study
STARTED
34
34
36
Overall Study
COMPLETED
32
30
29
Overall Study
NOT COMPLETED
2
4
7

Reasons for withdrawal

Reasons for withdrawal
Measure
Placebo
Participants received alogabat matching placebo, orally, once daily (QD) up to 12 weeks during the treatment period.
Alogabat 20 mg
Participants received alogabat, 20 milligrams (mg), orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Overall Study
Adverse Event
1
0
2
Overall Study
Non-compliance with Study Drug
1
0
0
Overall Study
Reason not Specified
0
1
3
Overall Study
Physician Decision
0
1
1
Overall Study
Withdrawal by Subject
0
2
1

Baseline Characteristics

A 12-Week Placebo-Controlled Study to Investigate the Efficacy, Safety, and Tolerability of RO7017773 in Participants Aged 15-45 Years With Autism Spectrum Disorder (ASD)

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Placebo
n=34 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Total
n=104 Participants
Total of all reporting groups
Age, Continuous
25.3 years
STANDARD_DEVIATION 8.1 • n=99 Participants
24.8 years
STANDARD_DEVIATION 7.1 • n=107 Participants
25.0 years
STANDARD_DEVIATION 7.5 • n=206 Participants
25.0 years
STANDARD_DEVIATION 7.5 • n=7 Participants
Sex: Female, Male
Female
9 Participants
n=99 Participants
8 Participants
n=107 Participants
9 Participants
n=206 Participants
26 Participants
n=7 Participants
Sex: Female, Male
Male
25 Participants
n=99 Participants
26 Participants
n=107 Participants
27 Participants
n=206 Participants
78 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
11 Participants
n=99 Participants
6 Participants
n=107 Participants
6 Participants
n=206 Participants
23 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
22 Participants
n=99 Participants
28 Participants
n=107 Participants
29 Participants
n=206 Participants
79 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
1 Participants
n=99 Participants
0 Participants
n=107 Participants
1 Participants
n=206 Participants
2 Participants
n=7 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Asian
1 Participants
n=99 Participants
1 Participants
n=107 Participants
1 Participants
n=206 Participants
3 Participants
n=7 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Black or African American
0 Participants
n=99 Participants
4 Participants
n=107 Participants
3 Participants
n=206 Participants
7 Participants
n=7 Participants
Race (NIH/OMB)
White
31 Participants
n=99 Participants
28 Participants
n=107 Participants
27 Participants
n=206 Participants
86 Participants
n=7 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=99 Participants
0 Participants
n=107 Participants
2 Participants
n=206 Participants
2 Participants
n=7 Participants
Race (NIH/OMB)
Unknown or Not Reported
2 Participants
n=99 Participants
1 Participants
n=107 Participants
3 Participants
n=206 Participants
6 Participants
n=7 Participants

PRIMARY outcome

Timeframe: Baseline to Week 12

Population: Efficacy population included all participants who gave informed consent, were randomized, and received at least one dose of double-blind study medication. Overall number analyzed is the number of participants with data available for analysis

Vineland-3 is a semi-structured interview that measures an individual's adaptive behavior across 3 domains: Communication, Socialization, and Daily Living skills. Each domain is composed of 3 subdomains. Subdomain raw score is based on item responses (3-point scale: 0=never present; 1=sometimes present; 2=usually present) and is calculated for each subdomain of the three main domains as the sum of the scores for each item within the subdomain. Raw scores of the 9 subdomains are used to derive Growth Scale Values (GSVs; range = 10-197). A conversion table for mapping raw scores to GSV scores is found in Appendix 3, Table B.2 in the Vineland-3 manual (Sparrow et al. 2016). GSV is a person-ability score used to track an individual's progress. Vineland-3 ABC Composite GSV score is calculated as the mean GSV score (summing the 9 GSV subdomain scores and dividing by 9; Vineland-3 ABC Composite GSV scores can range from 10-154). A higher score indicates better adaptive functioning.

Outcome measures

Outcome measures
Measure
Placebo
n=32 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=27 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=28 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Change From Baseline to Week 12 in the Adaptive Behavior Composite (ABC) Score of the Vineland Adaptive Behavior Scales, Third Edition (Vineland-3)
3.250 score on a scale
Interval 2.011 to 4.49
2.819 score on a scale
Interval 1.469 to 4.169
2.807 score on a scale
Interval 1.499 to 4.115

SECONDARY outcome

Timeframe: Up to Week 18

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.

An AE is an untoward medical occurrence in a participant administered a pharmaceutical product and regardless of the causal relationship with the treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom/disease temporally associated with the use of an investigational product, whether or not considered related to the investigational product.

Outcome measures

Outcome measures
Measure
Placebo
n=34 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Number of Participants With at Least One Adverse Events (AEs)
24 Participants
22 Participants
22 Participants

SECONDARY outcome

Timeframe: Up to Week 18

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.

An AE is an untoward medical occurrence in a participant administered a pharmaceutical product and regardless of causal relationship with the treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom/disease temporally associated with the use of an investigational product, whether or not considered related to investigational product. A SAE is any significant hazard, contraindication, side effect that is fatal or life-threatening, requires hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, is medically significant or requires intervention to prevent one or other of the outcomes listed above.

Outcome measures

Outcome measures
Measure
Placebo
n=34 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Number of Participants With at Least One Serious Adverse Events (SAEs)
0 Participants
0 Participants
0 Participants

SECONDARY outcome

Timeframe: Day 1 up to Week 12

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.

An AE is an untoward medical occurrence in a participant administered a pharmaceutical product and regardless of the causal relationship with the treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom/disease temporally associated with the use of an investigational product, whether or not considered related to the investigational product.

Outcome measures

Outcome measures
Measure
Placebo
n=34 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Number of Participants Discontinuing Treatment Due to AEs
1 Participants
0 Participants
2 Participants

SECONDARY outcome

Timeframe: Baseline up to Week 18

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.

C-SSRS=assessment tool used to assess lifetime suicidality of participant (at baseline) as well as any new instances of suicidality (C-SSRS since last visit). Structured interview prompts recollection of suicidal ideation, including intensity of ideation, behavior, and attempts with actual/potential lethality. Categories have binary responses (yes/no) and include Wish to be Dead; Non-specific Active Suicidal Thoughts; Active Suicidal Ideation with Any Methods (Not Plan) without Intent to Act; Active Suicidal Ideation with Some Intent to Act, without Specific Plan; Active Suicidal Ideation with Specific Plan and Intent, Preparatory Acts and Behavior; Aborted Attempt; Interrupted Attempt; Actual Attempt (non-fatal); Completed Suicide. Suicidal ideation/behavior is indicated by a "yes" answer to any of the listed categories. Score of 0 is assigned if no suicide risk is present. Score of 1 or higher= suicidal ideation or behavior. Categories with non-zero values are only reported here.

Outcome measures

Outcome measures
Measure
Placebo
n=34 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Number of Participants With Post-baseline Suicidal Ideation or Suicidal Behaviour as Measured Using the Columbia-Suicide-Severity Rating Scale (C-SSRS)
Wish to be Dead
2 Participants
1 Participants
1 Participants
Number of Participants With Post-baseline Suicidal Ideation or Suicidal Behaviour as Measured Using the Columbia-Suicide-Severity Rating Scale (C-SSRS)
Non-specific Active Suicidal Thoughts
1 Participants
1 Participants
1 Participants
Number of Participants With Post-baseline Suicidal Ideation or Suicidal Behaviour as Measured Using the Columbia-Suicide-Severity Rating Scale (C-SSRS)
Self-Injurious Behavior Without Suicidal Intent
1 Participants
0 Participants
1 Participants

SECONDARY outcome

Timeframe: Baseline (Day 1 Predose), 3-4 hours post-dose on Day 1, Predose and 3-4 hours post-dose on Days 14, 42, and 84

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not. Overall number analyzed is the number of participants with data available for analysis. Number analyzed is the number of participants with data available for analysis at the specified timepoint.

The KSS measures the subjective level of sleepiness at a particular time during the day. On this scale, participants (or support persons for adolescents aged 15 to 17 years and low-functioning participants) indicate which level best reflects the psycho-physical state experienced in the last 5 minutes. The KSS is a 9-point scale (1=extremely alert, 9=very sleepy, great effort to keep awake, fighting sleep). A decrease in KSS score or negative change from baseline indicate an improvement in sleepiness.

Outcome measures

Outcome measures
Measure
Placebo
n=33 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Change from Baseline at Day 84: Predose
-1.52 score on a scale
Standard Deviation 2.23
-0.83 score on a scale
Standard Deviation 2.65
-0.48 score on a scale
Standard Deviation 2.13
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Baseline (Day 1: Predose)
4.97 score on a scale
Standard Deviation 2.10
4.88 score on a scale
Standard Deviation 2.28
4.17 score on a scale
Standard Deviation 2.37
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Change from Baseline at Day 1: 3-4 hours Post Dose
-0.88 score on a scale
Standard Deviation 2.00
-0.58 score on a scale
Standard Deviation 2.12
0.19 score on a scale
Standard Deviation 2.20
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Change from Baseline at Day 14: Predose
-0.03 score on a scale
Standard Deviation 1.91
-0.13 score on a scale
Standard Deviation 2.12
-0.03 score on a scale
Standard Deviation 2.15
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Change from Baseline at Day 14: 3-4 hours Post Dose
-0.76 score on a scale
Standard Deviation 1.70
-0.84 score on a scale
Standard Deviation 2.60
0.34 score on a scale
Standard Deviation 2.72
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Change from Baseline at Day 42: Predose
-0.50 score on a scale
Standard Deviation 2.05
-0.94 score on a scale
Standard Deviation 2.66
-0.94 score on a scale
Standard Deviation 1.82
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Change from Baseline at Day 42: 3-4 hours Post Dose
-0.74 score on a scale
Standard Deviation 1.77
-1.00 score on a scale
Standard Deviation 2.79
-0.26 score on a scale
Standard Deviation 2.34
Change From Baseline in Karolinska Sleepiness Scale (KSS) Score for Assessing Daytime Sleepiness
Change from Baseline at Day 84: 3-4 hours Post Dose
-1.13 score on a scale
Standard Deviation 2.00
-0.83 score on a scale
Standard Deviation 2.80
-0.30 score on a scale
Standard Deviation 2.45

SECONDARY outcome

Timeframe: Baseline (Day 1), Days 14, 42, and 84

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not. Overall number analyzed is the number of participants with data available for analysis. Number analyzed is the number of participants with data available for analysis at the specified timepoint.

The ESS is a brief, self-administered eight-item questionnaire that measures daytime sleepiness in adults. Participants were asked to rate on a scale of 0-3 the chances that, "over the past month" and "since last visit", he/she would have dozed in eight specific situations that are commonly met in daily life (0 = would never doze and 3 = high chance of dozing). The ESS score is the sum of eight item-scores and can range from 0 to 24. A lower ESS score or a negative change from baseline score indicates an improvement in daytime sleepiness.

Outcome measures

Outcome measures
Measure
Placebo
n=26 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=26 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=26 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Change From Baseline in Epworth Sleepiness Scale Score (ESS) for Assessing Daytime Sleepiness
Baseline (Day 1)
5.00 score on a scale
Standard Deviation 3.69
6.15 score on a scale
Standard Deviation 4.23
4.54 score on a scale
Standard Deviation 2.67
Change From Baseline in Epworth Sleepiness Scale Score (ESS) for Assessing Daytime Sleepiness
Change from Baseline at Day 14
0.24 score on a scale
Standard Deviation 2.42
-0.72 score on a scale
Standard Deviation 3.36
0.73 score on a scale
Standard Deviation 4.58
Change From Baseline in Epworth Sleepiness Scale Score (ESS) for Assessing Daytime Sleepiness
Change from Baseline at Day 42
0.62 score on a scale
Standard Deviation 2.52
-2.08 score on a scale
Standard Deviation 4.15
0.50 score on a scale
Standard Deviation 3.39
Change From Baseline in Epworth Sleepiness Scale Score (ESS) for Assessing Daytime Sleepiness
Change from Baseline at Day 84
0.38 score on a scale
Standard Deviation 3.40
-1.46 score on a scale
Standard Deviation 4.28
0.26 score on a scale
Standard Deviation 3.41

SECONDARY outcome

Timeframe: Baseline (Day 1), Days 14, 42, 63, and 84

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not. Overall number analyzed is the number of participants with data available for analysis. Number analyzed is the number of participants with data available for analysis at the specified timepoint.

The ESS-CHAD is a brief, support person-administered eight-item questionnaire that measures daytime sleepiness in children and adolescents. Each item asked the support persons of adolescents and participants with an IQ score \<70 to rate on a scale of 0-3 the chances that "Over the past month," and "since last visit", "your child" would have dozed in eight specific situations that are commonly met in daily life ( 0 to 3 where 0 = would never doze and 3 = high chance of dozing). The ESS score is the sum of eight item scores and can range from 0 to 24. A lower ESS score or negative change from baseline score indicates an improvement in daytime sleepiness.

Outcome measures

Outcome measures
Measure
Placebo
n=5 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=5 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=7 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Change From Baseline ESS Score for Children and Adolescents (ESS-CHAD) for Assessing Daytime Sleepiness
Change from Baseline at Day 84
1.40 score on a scale
Standard Deviation 4.51
-1.25 score on a scale
Standard Deviation 4.19
-1.50 score on a scale
Standard Deviation 1.29
Change From Baseline ESS Score for Children and Adolescents (ESS-CHAD) for Assessing Daytime Sleepiness
Baseline (Day 1)
4.20 score on a scale
Standard Deviation 3.83
6.20 score on a scale
Standard Deviation 1.30
6.86 score on a scale
Standard Deviation 4.53
Change From Baseline ESS Score for Children and Adolescents (ESS-CHAD) for Assessing Daytime Sleepiness
Change from Baseline at Day 14
-1.00 score on a scale
Standard Deviation 2.92
-0.40 score on a scale
Standard Deviation 3.36
-1.00 score on a scale
Standard Deviation 2.28
Change From Baseline ESS Score for Children and Adolescents (ESS-CHAD) for Assessing Daytime Sleepiness
Change from Baseline at Day 42
-1.40 score on a scale
Standard Deviation 2.70
-2.00 score on a scale
Standard Deviation 2.16
1.00 score on a scale
Standard Deviation 2.92
Change From Baseline ESS Score for Children and Adolescents (ESS-CHAD) for Assessing Daytime Sleepiness
Change from Baseline at Day 63
-1.00 score on a scale
Standard Deviation 1.41
-2.50 score on a scale
Standard Deviation 0.71
-2.00 score on a scale
Standard Deviation 1.41

SECONDARY outcome

Timeframe: Baseline (Day 1), Days 7, 14, 42, 63, and 84

Population: Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not. Number analyzed is the number of participants with data available for analysis at specified timepoints.

A sleep questionnaire was developed specifically for this study. Each participant (or support person for adolescents aged 15 to 17 years and for low-functioning participants) was asked to answer a series of 8 questions. The questions and their corresponding responses are as follows: a. Have you ever fallen asleep or have you been likely to fall asleep during your waking time? (Yes/No); b. Was this episode? (Gradual with awareness/Sudden and unpredictable/Sudden with awareness); c. Of the recent episode, how often does this occur? (Every day/Less frequently/Once a week/Other); d. Do you feel worried about falling asleep during the day? (Yes/No); e. Did the episode (or episodes) disrupt your daily activities? (Considerably/Marginally/No); f. Did this episode (or episodes) disrupt your social life (Considerably/Marginally/No); g. In the case of such an episode, was awakening? (Difficult/Easy/Normal). Categories with non-zero values are only reported here.

Outcome measures

Outcome measures
Measure
Placebo
n=34 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 14 (No)
8 Participants
6 Participants
8 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 14 (Yes)
2 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 42 (No)
4 Participants
1 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 42 (Yes)
2 Participants
2 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 63 (No)
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 63 (Yes)
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 84 (No)
4 Participants
0 Participants
4 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 84 (Yes)
3 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Baseline: Day 1 (Considerably)
0 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Baseline: Day 1 (Marginally)
8 Participants
5 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Baseline: Day 1 (No)
4 Participants
1 Participants
6 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 7 (Considerably)
0 Participants
1 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 7 (Marginally)
1 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 7 (No)
0 Participants
6 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 14 (Considerably)
0 Participants
1 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 14 (Marginally)
3 Participants
1 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 14 (No)
7 Participants
5 Participants
5 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 42 (Marginally)
1 Participants
0 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 42 (No)
5 Participants
3 Participants
4 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 63 (Marginally)
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 63 (No)
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 84 (Considerably)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 84 (Marginally)
2 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
e. Day 84 (No)
5 Participants
1 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Baseline: Day 1 (Marginally)
3 Participants
3 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Baseline: Day 1 (No)
9 Participants
4 Participants
6 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 7 (Considerably)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 7 (Marginally)
0 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 7 (No)
1 Participants
7 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 14 (Considerably)
1 Participants
0 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 14 (Marginally)
0 Participants
1 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 14 (No)
9 Participants
6 Participants
5 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 42 (Considerably)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 42 (Marginally)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 42 (No)
6 Participants
3 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 63 (No)
1 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 84 (Considerably)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 84 (Marginally)
1 Participants
0 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
f. Day 84 (No)
6 Participants
1 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Baseline: Day 1 (Difficult)
1 Participants
0 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Baseline: Day 1 (Easy)
7 Participants
5 Participants
4 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Baseline: Day 1 (Normal)
4 Participants
2 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 7 (Easy)
1 Participants
5 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 7 (Normal)
0 Participants
3 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 14 (Easy)
6 Participants
5 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 14 (Normal)
4 Participants
2 Participants
5 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 42 (Easy)
4 Participants
3 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 42 (Normal)
2 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 63 (Easy)
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 63 (Normal)
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 84 (Easy)
6 Participants
1 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
g. Day 84 (Normal)
1 Participants
0 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Baseline: Day 1 (No)
22 Participants
28 Participants
29 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Baseline: Day 1 (Yes)
11 Participants
6 Participants
7 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 7 (No)
30 Participants
25 Participants
30 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 7 (Yes)
1 Participants
8 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 14 (No)
22 Participants
26 Participants
26 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 14 (Yes)
8 Participants
6 Participants
8 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 42 (No)
26 Participants
29 Participants
28 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 42 (Yes)
6 Participants
3 Participants
4 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 63 (No)
3 Participants
2 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 63 (Yes)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 84 (No)
26 Participants
30 Participants
27 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
a. Day 84 (Yes)
7 Participants
1 Participants
4 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Baseline: Day 1 (Gradual with Awareness)
10 Participants
5 Participants
6 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Baseline: Day 1 (Sudden and Unpredictable (Without Awareness))
1 Participants
0 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Baseline: Day 1 (Sudden with Awareness)
1 Participants
1 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 7 (Gradual with Awareness)
1 Participants
7 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 7 (Sudden and Unpredictable (Without Awareness))
0 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 7 (Sudden with Awareness)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 14 (Gradual with Awareness)
10 Participants
5 Participants
5 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 14 (Sudden and Unpredictable (Without Awareness))
0 Participants
2 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 14 (Sudden with Awareness)
0 Participants
0 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 42 (Gradual with Awareness)
6 Participants
3 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 42 (Sudden with Awareness)
1 Participants
0 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 63 (Gradual with Awareness)
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 63 (Sudden with Awareness)
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 84 (Gradual with Awareness)
7 Participants
1 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 84 (Sudden and Unpredictable (Without Awareness))
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
b. Day 84 (Sudden with Awareness)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Baseline: Day 1 (Everyday)
5 Participants
1 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Baseline: Day 1 (Less Frequently)
1 Participants
1 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Baseline: Day 1 (Once a Week)
4 Participants
4 Participants
3 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Baseline: Day 1 (Other)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 7 (Everyday)
0 Participants
0 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 7 (Less Frequently)
0 Participants
2 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 7 (Once a Month)
0 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 7 (Once a Week)
1 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 7 (Other)
0 Participants
4 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 14 (Everyday)
2 Participants
0 Participants
4 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 14 (Less Frequently)
0 Participants
3 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 14 (Once a Week)
6 Participants
2 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 14 (Other)
2 Participants
2 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 42 (Everyday)
3 Participants
0 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 42 (Less Frequently)
1 Participants
0 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 42 (Once a Month)
0 Participants
1 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 42 (Once a Week)
1 Participants
2 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 42 (Other)
1 Participants
0 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 63 (Everyday)
1 Participants
1 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 84 (Everyday)
0 Participants
0 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 84 (Less Frequently)
3 Participants
0 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 84 (Once a Week)
1 Participants
1 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
c. Day 84 (Other)
3 Participants
0 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Baseline: Day 1 (No)
5 Participants
3 Participants
7 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Baseline: Day 1 (Yes)
7 Participants
4 Participants
0 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 7 (No)
0 Participants
6 Participants
2 Participants
Number of Participants With Daytime Sleepiness Assessed Using Sudden Onset of Sleep Questionnaire
d. Day 7 (Yes)
1 Participants
2 Participants
0 Participants

SECONDARY outcome

Timeframe: Baseline to Week 12

Population: Efficacy population included all participants who gave informed consent, were randomized, and received at least one dose of double-blind study medication. Overall number analyzed is the number of participants with data available for analysis.

The RBS-R is a 43-item informant-based questionnaire, assessing the variety of restricted and repetitive behaviors (RRBs) in individuals with ASD. The scale is grouped into six subscales: Stereotyped, Self-Injurious, Compulsive, Ritualistic, Sameness, and Restricted Behaviors. For each item, behaviors are rated on a 4-point scale: 0-Behavior does not occur, 1-Behavior occurs and is a mild problem, 2-Behavior occurs and is a moderate problem, 3-Behavior occurs and is a severe problem. A total RBS-R score is calculated as the sum of the scores for the 43 items. The total score ranges from 0 to 129 and higher scores are indicative of more severe RRBs.

Outcome measures

Outcome measures
Measure
Placebo
n=30 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=29 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=28 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Change From Baseline to Week 12 in Behavior/Symptoms as Measured by All Domains of the Repetitive Behavior Scale-Revised (RBS-R) Score
-6.695 score on a scale
Interval -9.772 to -3.618
-4.954 score on a scale
Interval -8.071 to -1.836
-8.410 score on a scale
Interval -11.621 to -5.2

SECONDARY outcome

Timeframe: Baseline to Week 12

Population: Efficacy population included all participants who gave informed consent, were randomized, and received at least one dose of double-blind study medication. Overall number analyzed is the number of participants with data available for analysis

Vineland-3 is a semi-structured interview measuring an individual's adaptive behavior across 3 domains: Communication, Socialization \& Daily Living skills. Each domain consists of 3 subdomains. Subdomain raw scores are based on item responses (3-point scale: 0=never present; 1=sometimes present; 2=usually present) \& are calculated for each subdomain of Socialization (interpersonal relationships, play and leisure time, coping skills) domain as sum of the scores for each item in the subdomain. Raw scores for the 3 Socialization subdomains are used to derive GSVs (range=10-164). A conversion table for mapping raw scores to GSV scores is found in the Vineland-3 manual (Sparrow et al. 2016). GSV is a person-ability score used to track an individual's progress. Vineland-3 Socialization Domain GSV score is calculated as a mean GSV score (summing the 3 GSV subdomain scores \& dividing by 3). Vineland-3 Socialization Domain GSV score range = 10-145. Higher score =better adaptive functioning.

Outcome measures

Outcome measures
Measure
Placebo
n=31 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=27 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=29 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Change From Baseline to Week 12 on the Vineland-3 Socialization Domain
6.298 score on a scale
Interval 4.302 to 8.294
3.315 score on a scale
Interval 1.162 to 5.468
1.824 score on a scale
Interval -0.22 to 3.868

SECONDARY outcome

Timeframe: Baseline to Week 12

Population: Efficacy population included all participants who gave informed consent, were randomized, and received at least one dose of double-blind study medication. Overall number analyzed is the number of participants with data available for analysis.

Vineland-3 is a semi-structured interview measuring an individual's adaptive behavior across 3 domains: Communication, Socialization \& Daily Living skills. Each domain consists of 3 subdomains. Subdomain raw scores are based on item responses (3-point scale: 0=never present; 1=sometimes present; 2=usually present) \& is calculated for each subdomain of the Communication (receptive, expressive, written) domain as the sum of the scores for each item within the subdomain. Raw scores for each of the 3 Communication subdomains are used to derive Growth Scale Values (GSVs; range from 10-197). A conversion table for mapping raw scores to GSV scores is found in Vineland-3 manual (Sparrow et al. 2016). GSV is a person-ability score used to track an individual's progress. Vineland-3 Socialization Domain GSV score is calculated as mean GSV score (summing the 3 GSV subdomain scores \& dividing by 3). Vineland-3 Socialization Domain GSV score range=10-174. Higher score=better adaptive functioning.

Outcome measures

Outcome measures
Measure
Placebo
n=32 Participants
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=27 Participants
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=28 Participants
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
Change From Baseline to Week 12 on the Vineland-3 Communication Domain
1.624 score on a scale
Interval 0.087 to 3.162
2.903 score on a scale
Interval 1.228 to 4.578
4.321 score on a scale
Interval 2.693 to 5.948

Adverse Events

Placebo

Serious events: 0 serious events
Other events: 16 other events
Deaths: 0 deaths

Alogabat 20 mg

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

Alogabat 60 mg

Serious events: 0 serious events
Other events: 17 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Other adverse events
Measure
Placebo
n=34 participants at risk
Participants received alogabat matching placebo, orally, QD up to 12 weeks during the treatment period.
Alogabat 20 mg
n=34 participants at risk
Participants received alogabat, 20 mg, orally, QD up to 12 weeks during the treatment period.
Alogabat 60 mg
n=36 participants at risk
Participants received alogabat, 60 mg, orally, QD up to 12 weeks during the treatment period.
General disorders
Fatigue
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.9%
2/34 • Number of events 5 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
8.3%
3/36 • Number of events 4 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Infections and infestations
Gastroenteritis
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.9%
2/34 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.8%
1/36 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Infections and infestations
Nasopharyngitis
2.9%
1/34 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
8.8%
3/34 • Number of events 3 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.8%
1/36 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Infections and infestations
Rhinitis
5.9%
2/34 • Number of events 4 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
0.00%
0/36 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Injury, poisoning and procedural complications
Ligament sprain
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.9%
2/34 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
0.00%
0/36 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Injury, poisoning and procedural complications
Road traffic accident
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.9%
2/34 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
0.00%
0/36 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Nervous system disorders
Dizziness
5.9%
2/34 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.9%
1/34 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.6%
2/36 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Nervous system disorders
Headache
14.7%
5/34 • Number of events 7 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
8.8%
3/34 • Number of events 7 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.6%
2/36 • Number of events 12 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Nervous system disorders
Hypersomnia
5.9%
2/34 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
8.8%
3/34 • Number of events 3 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
8.3%
3/36 • Number of events 3 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Nervous system disorders
Lethargy
5.9%
2/34 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.9%
1/34 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
0.00%
0/36 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Nervous system disorders
Somnolence
14.7%
5/34 • Number of events 8 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
20.6%
7/34 • Number of events 7 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
16.7%
6/36 • Number of events 12 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Nervous system disorders
Sudden onset of sleep
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
8.8%
3/34 • Number of events 6 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.6%
2/36 • Number of events 3 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Psychiatric disorders
Anxiety
8.8%
3/34 • Number of events 3 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.9%
1/34 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.8%
1/36 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Psychiatric disorders
Irritability
5.9%
2/34 • Number of events 3 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.9%
1/34 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
11.1%
4/36 • Number of events 4 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Respiratory, thoracic and mediastinal disorders
Cough
5.9%
2/34 • Number of events 4 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.9%
1/34 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.8%
1/36 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Gastrointestinal disorders
Dyspepsia
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
5.9%
2/34 • Number of events 2 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
0.00%
0/36 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
Gastrointestinal disorders
Nausea
0.00%
0/34 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
2.9%
1/34 • Number of events 1 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.
11.1%
4/36 • Number of events 8 • Up to Week 18
Safety population included all participants randomized to study treatment and who received at least one dose of the study treatment, whether prematurely withdrawn from the study or not.

Additional Information

Medical Communications

Hoffmann-La Roche

Phone: 800 821-8590

Results disclosure agreements

  • Principal investigator is a sponsor employee The Study being conducted under this Agreement is part of the Overall Study. Investigator is free to publish in reputable journals or to present at professional conferences the results of the Study, but only after the first publication or presentation that involves the Overall Study. The Sponsor may request that Confidential Information be deleted and/or the publication be postponed in order to protect the Sponsor's intellectual property rights.
  • Publication restrictions are in place

Restriction type: OTHER