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Clinical Trial Results:
Phase III, Randomized, Double-Blind, Double-Dummy, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy (Induction of Remission) and Safety of Etrolizumab Compared With Adalimumab and Placebo in Patients With Moderate to Severe Ulcerative Colitis who are Naive to TNF Inhibitors

Summary
EudraCT number	2013-004279-11
Trial protocol	EE BG SK FR
Global end of trial date	19 Mar 2020

Results information
Results version number	v1
This version publication date	14 Feb 2021
First version publication date	14 Feb 2021
Other versions	v2

Trial Information
Subject Disposition
Baseline Characteristics
End Points
Adverse Events
More Information

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Trial information

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Sponsor protocol code

GA28948

ISRCTN number

US NCT number

NCT02163759

WHO universal trial number (UTN)

Sponsor organisation name

F. Hoffmann-La Roche, Ltd.

Sponsor organisation address

Grenzacherstrasse 124, Basel, Switzerland, CH-4070

Public contact

F. Hoffmann-La Roche, Ltd., F. Hoffmann-La Roche, Ltd., 41 616878333, global.trial_information@roche.com

Scientific contact

F. Hoffmann-La Roche, Ltd., F. Hoffmann-La Roche, Ltd., 41 616878333, global.trial_information@roche.com

Is trial part of an agreed paediatric investigation plan (PIP)

Does article 45 of REGULATION (EC) No 1901/2006 apply to this trial?

Does article 46 of REGULATION (EC) No 1901/2006 apply to this trial?

Analysis stage

Final

Date of interim/final analysis

19 Mar 2020

Is this the analysis of the primary completion data?

Yes

Primary completion date

19 Feb 2020

Global end of trial reached?

Yes

Global end of trial date

19 Mar 2020

Was the trial ended prematurely?

Main objective of the trial

-To evaluate the efficacy of etrolizumab (105 mg SC every 4 weeks [Q4W]) compared with placebo for the induction of remission in TNF-naive patients with ulcerative colitis as determined by the Mayo Clinic Score at Week 10

Protection of trial subjects

This study was conducted in full conformance with the ICH E6 guideline for Good Clinical Practice and the principles of the Declaration of Helsinki or the laws and regulations of the country in which the research is conducted, whichever afforded the greater protection to the individual. All subjects signed an informed consent form before participating in the study.

Background therapy

During the induction phase (Day 1 to Week 10), continuation of stable baseline doses of the following non-investigational medicinal products were permitted: oral 5-aminosalicylic acid (5-ASA); azathioprine; 6-mercaptopurine; methotrexate; corticosteroids up to 30 milligrams per day (mg/day) of prednisone (or equivalent); and budesonide up to 9 mg/day. From Week 10 to Week 14, subjects who achieved clinical remission at Week 10 were to continue immunosuppressants (AZA, 6-MP, MTX) at a stable dose unless dose reduction or discontinuation was required due to immunosuppressant-related toxicity. For subjects who stayed in the study, corticosteroids were to be tapered starting from Week 10 in those who achieved clinical remission. Throughout the study, probiotics and oral 5-ASA may have been continued at a stable dose. Occasional use of NSAIDs and acetaminophen (e.g., for headache, arthritis, myalgias, menstrual cramps) and aspirin up to 325 mg daily were permitted throughout the study. Antidiarrheals (e.g., loperamide, diphenoxylate with atropine) for control of chronic diarrhea were permitted throughout the study.

Evidence for comparator

Actual start date of recruitment

04 Nov 2014

Long term follow-up planned

Independent data monitoring committee (IDMC) involvement?

Yes

Number of subjects enrolled per country

Country: Number of subjects enrolled

Argentina: 1

Country: Number of subjects enrolled

Australia: 15

Country: Number of subjects enrolled

Bulgaria: 5

Country: Number of subjects enrolled

Brazil: 36

Country: Number of subjects enrolled

Estonia: 15

Country: Number of subjects enrolled

France: 3

Country: Number of subjects enrolled

Hong Kong: 1

Country: Number of subjects enrolled

Mexico: 4

Country: Number of subjects enrolled

Poland: 79

Country: Number of subjects enrolled

Russian Federation: 57

Country: Number of subjects enrolled

Serbia: 33

Country: Number of subjects enrolled

Slovakia: 29

Country: Number of subjects enrolled

Ukraine: 68

Country: Number of subjects enrolled

United States: 12

Worldwide total number of subjects

358

EEA total number of subjects

131

Number of subjects enrolled per age group

In utero

Preterm newborn - gestational age < 37 wk

Newborns (0-27 days)

Infants and toddlers (28 days-23 months)

Children (2-11 years)

Adolescents (12-17 years)

Adults (18-64 years)

337

From 65 to 84 years

85 years and over

Subject disposition

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Recruitment details

Screening details

Subjects on concomitant background therapy were allowed to continue receiving stable baseline doses of the following non-investigational medicinal products during the study: oral 5-ASA; azathioprine; 6-mercaptopurine; methotrexate; corticosteroids up to 30 mg/day of prednisone (or equivalent); and/or budesonide up to 9 mg/day.

Period 1 title

Overall Study (overall period)

Is this the baseline period?

Yes

Allocation method

Randomised - controlled

Blinding used

Double blind

Roles blinded

Subject, Investigator

Are arms mutually exclusive

Yes

Placebo

Arm description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive placebo matching to etrolizumab subcutaneously (SC) once every 4 weeks (Q4W) up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]) and placebo matching to adalimumab SC once every 2 weeks (Q2W) up to Week 8 (at Weeks 0 [Day 1], 2, 4, 6, and 8).

Arm type

Placebo

Investigational medicinal product name

Etrolizumab Placebo

Investigational medicinal product code

Other name

Pharmaceutical forms

Solution for injection in pre-filled syringe

Routes of administration

Subcutaneous use

Dosage and administration details

The placebo matching to etrolizumab was supplied in a pre-filled syringe and was administered as an SC injection once every 4 weeks up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]).

Investigational medicinal product name

Adalimumab Placebo

Investigational medicinal product code

Other name

Pharmaceutical forms

Solution for injection in pre-filled syringe

Routes of administration

Subcutaneous use

Dosage and administration details

The placebo matching to adalimumab was supplied in a pre-filled syringe and was administered as an SC injection once every 2 weeks (Q2W) up to Week 8 (at Weeks 0 [Day 1], 2, 4, 6, and 8).

Adalimumab

Arm description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive adalimumab subcutaneously (SC) Q2W up to Week 8 (160 mg at Week 0 [Day 1], 80 mg at Week 2, 40 mg at Weeks 4, 6, and 8) and placebo matching to etrolizumab SC Q4W up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]).

Arm type

Active comparator

Investigational medicinal product name

Adalimumab

Investigational medicinal product code

Other name

Humira

Pharmaceutical forms

Solution for injection in pre-filled syringe

Routes of administration

Subcutaneous use

Dosage and administration details

Adalimumab was supplied in a pre-filled syringe and was administered as an SC injection once every 2 weeks (Q2W) up to Week 8 (at Weeks 0 [Day 1], 2, 4, 6, and 8). Adalimumab was to be administered at a dose of 160 milligrams (mg) at Week 0 (Day 1; 4 injections), 80 mg at Week 2 (2 injections), and 40 mg (1 injection) at Weeks 4, 6, and 8.

Investigational medicinal product name

Etrolizumab Placebo

Investigational medicinal product code

Other name

Pharmaceutical forms

Solution for injection in pre-filled syringe

Routes of administration

Subcutaneous use

Dosage and administration details

Etrolizumab

Arm description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive etrolizumab 105 mg subcutaneously (SC) Q4W up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]) and placebo matching to adalimumab SC Q2W up to Week 8 (at Weeks 0 [Day 1], 2, 4, 6, and 8).

Arm type

Experimental

Investigational medicinal product name

Adalimumab Placebo

Investigational medicinal product code

Other name

Pharmaceutical forms

Solution for injection in pre-filled syringe

Routes of administration

Subcutaneous use

Dosage and administration details

The placebo matching to adalimumab was supplied in a pre-filled syringe and was administered as an SC injection once every 2 weeks (Q2W) up to Week 8 (at Weeks 0 [Day 1], 2, 4, 6, and 8).

Investigational medicinal product name

Etrolizumab

Investigational medicinal product code

RO5490261

Other name

PRO145223

Pharmaceutical forms

Solution for injection in pre-filled syringe

Routes of administration

Subcutaneous use

Dosage and administration details

Etrolizumab was supplied in a pre-filled syringe and was administered as an SC injection at a dose of 105 mg once every 4 weeks up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]).

Number of subjects in period 1	Placebo	Adalimumab	Etrolizumab
Started	72	142	144
Completed Week 10	71	141	143
Completed	71	137	141
Not completed	1	5	3
Adverse event, serious fatal	-	-	1
Consent withdrawn by subject	1	5	1
Adverse event, non-fatal	-	-	1

Baseline characteristics

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Reporting group title

Placebo

Reporting group description

Reporting group title

Adalimumab

Reporting group description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive adalimumab subcutaneously (SC) Q2W up to Week 8 (160 mg at Week 0 [Day 1], 80 mg at Week 2, 40 mg at Weeks 4, 6, and 8) and placebo matching to etrolizumab SC Q4W up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]).

Reporting group title

Etrolizumab

Reporting group description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive etrolizumab 105 mg subcutaneously (SC) Q4W up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]) and placebo matching to adalimumab SC Q2W up to Week 8 (at Weeks 0 [Day 1], 2, 4, 6, and 8).

Reporting group values	Placebo	Adalimumab	Etrolizumab	Total
Number of subjects	72	142	144	358
Age categorical
Units: Subjects
In utero	0	0	0	0
Preterm newborn infants (gestational age < 37 wks)	0	0	0	0
Newborns (0-27 days)	0	0	0	0
Infants and toddlers (28 days-23 months)	0	0	0	0
Children (2-11 years)	0	0	0	0
Adolescents (12-17 years)	0	0	0	0
Adults (18-64 years)	69	133	135	337
From 65-84 years	3	9	9	21
85 years and over	0	0	0	0
Age Continuous
Units: Years
arithmetic mean (standard deviation)	38.4 ± 13.3	42.0 ± 13.8	40.1 ± 13.4	-
Sex: Female, Male
Units: Participants
Female	33	60	70	163
Male	39	82	74	195
Race/Ethnicity, Customized
Units: Subjects
Asian	0	2	0	2
Black or African American	2	0	1	3
White	68	130	138	336
Other	2	10	5	17
Ethnicity (NIH/OMB)
Units: Subjects
Hispanic or Latino	8	16	14	38
Not Hispanic or Latino	63	123	128	314
Unknown or Not Reported	1	3	2	6
Disease Location
Units: Subjects
Left-Sided Colitis	44	84	89	217
Extensive Colitis	10	23	22	55
Pancolitis	18	35	33	86
Mayo Clinic Score (MCS) ≤9 or ≥10 at Baseline
Participants were stratified by concomitant treatment with corticosteroids (yes/no) at randomization, concomitant treatment with immunosuppressants (yes/no) at randomization, and disease activity measured during screening (MCS ≤9/MCS ≥10). The MCS ranges from 0 to 12 and is a composite of the four following assessments of disease activity: stool frequency subscore, rectal bleeding subscore, endoscopy subscore, and physician's global assessment (PGA) subscore. Each of the four assessments was rated with a score from 0 to 3, with higher scores indicating more severe disease.
Units: Subjects
MCS ≤9	47	96	100	243
MCS ≥10	25	46	44	115
Baseline Treatment: None, Corticosteroids (CS) or Immunosuppressants (IS) Alone, or Both CS and IS
Participants were stratified by concomitant treatment with corticosteroids (yes/no) at randomization, concomitant treatment with immunosuppressants (yes/no) at randomization, and disease activity measured during screening (MCS ≤9/MCS ≥10).
Units: Subjects
None	24	51	45	120
Corticosteroids (CS) Alone	25	46	50	121
Immunosuppressants (IS) Alone	15	30	32	77
Both CS and IS	8	15	17	40
Nancy Histological Index (NHI) Score of ≤1 or >1, or Missing, at Baseline
Histologic disease activity was measured using the Nancy Histological Index (NHI) score, ranging from 0 to 4, with the following definitions for each grade: 0 is no histologically significant disease; 1 is chronic inflammatory infiltrate with no acute inflammatory infiltrate; and 2, 3, and 4 are mildly, moderately, and severely active disease, respectively.
Units: Subjects
NHI Score ≤1	8	15	15	38
NHI Score >1	62	116	120	298
Missing	2	11	9	22

End points

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Reporting group title

Placebo

Reporting group description

Reporting group title

Adalimumab

Reporting group description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive adalimumab subcutaneously (SC) Q2W up to Week 8 (160 mg at Week 0 [Day 1], 80 mg at Week 2, 40 mg at Weeks 4, 6, and 8) and placebo matching to etrolizumab SC Q4W up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]).

Reporting group title

Etrolizumab

Reporting group description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive etrolizumab 105 mg subcutaneously (SC) Q4W up to Week 12 (at Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]) and placebo matching to adalimumab SC Q2W up to Week 8 (at Weeks 0 [Day 1], 2, 4, 6, and 8).

Primary: Percentage of Participants in Remission With Etrolizumab Compared With Placebo at Week 10, as Determined by the Mayo Clinic Score (MCS)

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End point title

Percentage of Participants in Remission With Etrolizumab Compared With Placebo at Week 10, as Determined by the Mayo Clinic Score (MCS) ^[1]

End point description

The Mayo Clinic Score (MCS) ranges from 0 to 12 and is a composite of the four following assessments of disease activity: stool frequency subscore, rectal bleeding subscore, endoscopy subscore, and physician's global assessment (PGA) subscore. Each of the four assessments was rated with a score from 0 to 3, with higher scores indicating more severe disease. Remission was defined as MCS less than or equal to (≤)2 with individual subscores ≤1 and a rectal bleeding subscore of 0. Participants were also classified as non-remitters if Week 10 assessments were missing or if they had received permitted/prohibited rescue therapy prior to assessment. Participants were stratified by concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening (MCS ≤9/MCS ≥10); the Cochran-Mantel-Haenszel test adjusted the difference in remission rates and associated 95% confidence interval for the stratification factors.

End point type

Primary

End point timeframe

Week 10

Notes
[1] - The end point is not reporting statistics for all the arms in the baseline period. It is expected all the baseline period arms will be reported on when providing values for an end point on the baseline period.
Justification: The primary outcome measure only compared remission rates between the etrolizumab and placebo arms.

End point values	Placebo	Etrolizumab
Number of subjects analysed	72	144
Units: Percentage of participants
number (confidence interval 95%)	6.9 (3.00 to 15.25)	19.4 (13.81 to 26.67)

Etrolizumab vs. Placebo: Remission at Week 10

Statistical analysis description

The null hypothesis (H0): the percentage of participants achieving remission at Week 10 was the same in both the placebo and etrolizumab arms. The alternative hypothesis (H1): the percentage of participants achieving remission at Week 10 was not the same in the placebo and etrolizumab arms.

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.0173 ^[2]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

12.3

Confidence interval

level

95%

sides

2-sided

lower limit

1.59

upper limit

20.6

Notes
[2] - The threshold for statistical significance was a p-value <0.05.

Secondary: Percentage of Participants in Remission With Etrolizumab Compared With Adalimumab at Week 10, as Determined by the MCS

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End point title

Percentage of Participants in Remission With Etrolizumab Compared With Adalimumab at Week 10, as Determined by the MCS ^[3]

End point description

The Mayo Clinic Score (MCS) ranges from 0 to 12 and is a composite of the four following assessments of disease activity: stool frequency subscore, rectal bleeding subscore, endoscopy subscore, and physician's global assessment (PGA) subscore. Each of the four assessments was rated with a score from 0 to 3, with higher scores indicating more severe disease. Remission was defined as MCS less than or equal to (≤)2 with individual subscores ≤1 and a rectal bleeding subscore of 0. Participants were also classified as non-remitters if Week 10 assessments were missing or if they had received permitted/prohibited rescue therapy prior to assessment. Participants were stratified by concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening (MCS ≤9/MCS ≥10). The Cochran-Mantel-Haenszel test adjusted the difference in remission rates and associated 95% confidence interval for the stratification factors.

End point type

Secondary

End point timeframe

Week 10

Notes
[3] - The end point is not reporting statistics for all the arms in the baseline period. It is expected all the baseline period arms will be reported on when providing values for an end point on the baseline period.
Justification: The secondary outcome measure of participants in remission only compared remission rates between the etrolizumab and adalimumab arms.

End point values	Adalimumab	Etrolizumab
Number of subjects analysed	142	144
Units: Percentage of participants
number (confidence interval 95%)	22.5 (16.44 to 30.08)	19.4 (13.81 to 26.67)

Etrolizumab vs. Adalimumab: Remission at Week 10

Statistical analysis description

Primary and secondary outcome measures were evaluated for statistical significance in a hierarchical manner with a component-wise multistage gatekeeping procedure. Please refer to the statistical analysis plan for details. Individual study results are shown, however, this endpoint was formally tested using pooled study data from this study and an identically designed study (GA28949); those pooled results cannot be provided on the registry due to its limitations.

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.5055 ^[4]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

-3.1

Confidence interval

level

95%

sides

2-sided

lower limit

-12.61

upper limit

6.37

Notes
[4] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Percentage of Participants in Clinical Remission at Week 10, as Determined by the MCS

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End point title

Percentage of Participants in Clinical Remission at Week 10, as Determined by the MCS

End point description

The Mayo Clinic Score (MCS) ranges from 0 to 12 and is a composite of the four following assessments of disease activity: stool frequency subscore, rectal bleeding subscore, endoscopy subscore, and physician's global assessment (PGA) subscore. Each of the four assessments was rated with a score from 0 to 3, with higher scores indicating more severe disease. Clinical remission was defined as MCS less than or equal to (≤)2 with individual subscores ≤1. Participants were also classified as non-remitters if Week 10 assessments were missing or if they had received permitted/prohibited rescue therapy prior to assessment. Participants were stratified by concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening (MCS ≤9/MCS ≥10). The Cochran-Mantel-Haenszel test adjusted the differences in remission rates and associated 95% confidence intervals for the stratification factors.

End point type

Secondary

End point timeframe

Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Percentage of participants
number (confidence interval 95%)	8.3 (3.88 to 17.01)	23.9 (17.67 to 31.59)	19.4 (13.81 to 26.67)

Etro vs. Placebo: Clinical Remission at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.0364 ^[5]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

10.9

Confidence interval

level

95%

sides

2-sided

lower limit

-0.08

upper limit

19.48

Notes
[5] - Nominal p-value; it has not been adjusted for multiplicity.

Etro vs. Adalimumab: Clinical Remission at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.3383 ^[6]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

-4.5

Confidence interval

level

95%

sides

2-sided

lower limit

-14.1

upper limit

5.07

Notes
[6] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Percentage of Participants With Clinical Response at Week 10, as Determined by the MCS

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End point title

Percentage of Participants With Clinical Response at Week 10, as Determined by the MCS

End point description

The Mayo Clinic Score (MCS) ranges from 0 to 12 and is a composite of the four following assessments of disease activity: stool frequency subscore, rectal bleeding subscore, endoscopy subscore, and physician's global assessment subscore. Each of the four assessments was rated with a score from 0 to 3, with higher scores indicating more severe disease. Clinical Response was defined as: MCS ≥3-point decrease and 30% reduction from baseline as well as ≥1-point decrease in rectal bleeding subscore or an absolute rectal bleeding score of 0 or 1. Non-responders also included participants with missing Week 10 assessments or those who had received permitted/prohibited rescue therapy prior to assessment. Participants were stratified by concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening (MCS ≤9 or ≥10); the CMH test adjusted the differences in response rates and associated 95% CIs for the stratification factors.

End point type

Secondary

End point timeframe

Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Percentage of participants
number (confidence interval 95%)	50.0 (38.75 to 61.25)	52.1 (43.95 to 60.16)	56.9 (48.78 to 64.75)

Etro vs. Placebo: Clinical Response at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.4434 ^[7]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Response Rates

Point estimate

6.9

Confidence interval

level

95%

sides

2-sided

lower limit

-7.03

upper limit

20.62

Notes
[7] - p-value has been adjusted for multiplicity.

Etro vs. Adalimumab: Clinical Response at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.4122 ^[8]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Response Rates

Point estimate

4.8

Confidence interval

level

95%

sides

2-sided

lower limit

-6.72

upper limit

16.07

Notes
[8] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Percentage of Participants With Improvement in Endoscopic Appearance of the Mucosa at Week 10, as Determined by the MCS Endoscopy Subscore

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End point title

Percentage of Participants With Improvement in Endoscopic Appearance of the Mucosa at Week 10, as Determined by the MCS Endoscopy Subscore

End point description

Improvement in endoscopic appearance of the mucosa was defined as a Mayo Clinic Score (MCS) endoscopy subscore ≤1. Blinded gastroenterologists experienced in inflammatory bowel disease performed central reading of endoscopies at an independent review facility. The rectum, sigmoid, and descending colon segments were assessed and each segment was assigned a score of 0 to 3, with higher scores indicating more severe disease. At baseline all segments were reviewed and the worst score from the three segments was recorded as the endoscopy subscore. Post-baseline the endoscopy score was the worst score of all segments that had been assessed at baseline, if the baseline endoscopy score had a sigmoid colon score ≤1. If at baseline the sigmoid colon score was ≥2, the post-baseline endoscopy score was the sigmoid colon score value. Non-responders also included participants with missing Week 10 assessments or those who had received permitted/prohibited rescue therapy prior to assessment.

End point type

Secondary

End point timeframe

Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Percentage of participants
number (confidence interval 95%)	22.2 (14.17 to 33.09)	33.1 (25.89 to 41.19)	40.3 (32.62 to 48.44)

Etro vs. Placebo: Endoscopic Appearance at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.0173 ^[9]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Response Rates

Point estimate

17.9

Confidence interval

level

95%

sides

2-sided

lower limit

4.49

upper limit

29.5

Notes
[9] - p-value has been adjusted for multiplicity.

Etro vs. Ada.: Endoscopic Appearance at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.1886 ^[10]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Response Rates

Point estimate

7.4

Confidence interval

level

95%

sides

2-sided

lower limit

-3.77

upper limit

18.32

Notes
[10] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Percentage of Participants in Endoscopic Remission at Week 10, as Determined by the MCS Endoscopy Subscore

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End point title

Percentage of Participants in Endoscopic Remission at Week 10, as Determined by the MCS Endoscopy Subscore

End point description

Endoscopic remission was defined as a Mayo Clinic Score (MCS) endoscopy subscore of 0. Blinded gastroenterologists experienced in inflammatory bowel disease performed central reading of endoscopies at an independent review facility. The rectum, sigmoid, and descending colon segments were assessed and each segment was assigned a score of 0 to 3, with higher scores indicating more severe disease. At baseline all segments were reviewed and the worst score from the three segments was recorded as the endoscopy subscore. Post-baseline the endoscopy score was the worst score of all segments that had been assessed at baseline, if the baseline endoscopy score had a sigmoid colon score ≤1. If at baseline the sigmoid colon score was ≥2, the post-baseline endoscopy score was the sigmoid colon score value. Non-responders also included participants with missing Week 10 assessments or those who had received permitted/prohibited rescue therapy prior to assessment.

End point type

Secondary

End point timeframe

Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Percentage of participants
number (confidence interval 95%)	6.9 (3.00 to 15.25)	20.4 (14.61 to 27.79)	20.8 (15.00 to 28.18)

Etro vs. Placebo: Endoscopic Remission at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.1347 ^[11]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

13.8

Confidence interval

level

95%

sides

2-sided

lower limit

2.97

upper limit

22.15

Notes
[11] - p-value has been adjusted for multiplicity.

Etro vs. Ada.: Endoscopic Remission at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.9138 ^[12]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

0.5

Confidence interval

level

95%

sides

2-sided

lower limit

-8.95

upper limit

9.92

Notes
[12] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Percentage of Participants in Remission at Week 10 and Week 14, as Determined by the MCS

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End point title

Percentage of Participants in Remission at Week 10 and Week 14, as Determined by the MCS

End point description

The Mayo Clinic Score (MCS) ranges from 0 to 12 and is a composite of the four following assessments of disease activity: stool frequency subscore, rectal bleeding subscore, endoscopy subscore, and physician's global assessment (PGA) subscore. Each of the four assessments was rated with a score from 0 to 3, with higher scores indicating more severe disease. Remission was defined as MCS less than or equal to (≤)2 with individual subscores ≤1 and a rectal bleeding subscore of 0. Participants were also classified as non-remitters if Week 10 or 14 assessments were missing or the participant received permitted/prohibited rescue therapy prior to assessment. Participants were stratified by concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening (MCS ≤9/MCS ≥10). The Cochran-Mantel-Haenszel test adjusted the differences in remission rates and associated 95% confidence intervals for the stratification factors.

End point type

Secondary

End point timeframe

Weeks 10 and 14

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Percentage of participants
number (confidence interval 95%)	2.8 (0.77 to 9.57)	12.7 (8.17 to 19.15)	9.0 (5.35 to 14.83)

Etro vs. Placebo: Remission at Weeks 10 and 14

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.09 ^[13]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

6.2

Confidence interval

level

95%

sides

2-sided

lower limit

-3.33

upper limit

12.3

Notes
[13] - Nominal p-value; it has not been adjusted for multiplicity.

Etro vs. Ada.: Remission at Weeks 10 and 14

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.3217 ^[14]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

-3.6

Confidence interval

level

95%

sides

2-sided

lower limit

-11.07

upper limit

3.78

Notes
[14] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Percentage of Participants With Histologic Remission at Week 10, as Determined by the Nancy Histological Index

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End point title

Percentage of Participants With Histologic Remission at Week 10, as Determined by the Nancy Histological Index

End point description

Histologic remission is defined by the resolution of neutrophilic inflammation (e.g., absence of neutrophils in the crypts and lamina propria), defined by a Nancy Histological Index (NHI) score of ≤1. The NHI score ranges from 0 to 4, with the following definitions for each grade: 0 is no histologically significant disease; 1 is chronic inflammatory infiltrate with no acute inflammatory infiltrate; and 2, 3, and 4 are mildly, moderately, and severely active disease, respectively. A small pool of central readers who were blinded to both treatment arm and timepoint performed the histologic scoring. The same reader scored all slides for a given participant based on biopsies from the most inflamed region of the sigmoid colon. Participants were also classified as non-remitters if Week 10 assessments were missing or if they had received rescue therapy prior to assessment. The Cochran-Mantel-Haenszel test adjusted the difference in remission rates and 95% CI for the stratification factors.

End point type

Secondary

End point timeframe

Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	62 ^[15]	116 ^[16]	120 ^[17]
Units: Percentage of participants
number (confidence interval 95%)	16.1 (9.00 to 27.21)	29.3 (21.80 to 38.15)	42.5 (34.02 to 51.44)

Notes
[15] - Subjects analyzed only includes those with NHI score >1 at baseline.
[16] - Subjects analyzed only includes those with NHI score >1 at baseline.
[17] - Subjects analyzed only includes those with NHI score >1 at baseline.

Etro vs. Placebo: Histologic Remission at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

182

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.0173 ^[18]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

26.3

Confidence interval

level

95%

sides

2-sided

lower limit

12.1

upper limit

37.86

Notes
[18] - p-value has been adjusted for multiplicity.

Etro vs. Ada.: Histologic Remission at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

236

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.0313 ^[19]

Method

Cochran-Mantel-Haenszel

Parameter type

Difference in Remission Rates

Point estimate

13.2

Confidence interval

level

95%

sides

2-sided

lower limit

0.93

upper limit

24.94

Notes
[19] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Change from Baseline in MCS Rectal Bleeding Subscore at Week 6

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End point title

Change from Baseline in MCS Rectal Bleeding Subscore at Week 6

End point description

Rectal bleeding data were collected via the participant’s diaries and each day a participant provided a score from 0 to 3 according to the following definitions: 0 = no blood in the stool; 1 = streaks of blood with stool less than half the time; 2 = obvious blood with stool most of the time; 3 = blood alone passed. The Mayo Clinic Score (MCS) rectal bleeding subscore was calculated as the worst value of three days of daily diary scores closest to anchor dates at baseline and post-baseline. The data was considered non-parametric and was reported using RANK analysis of covariance (ANCOVA). Participants were stratified by concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening (MCS ≤9/MCS ≥10); the model adjusted for these stratification factors along with the baseline rectal bleeding (RB) subscore.

End point type

Secondary

End point timeframe

Baseline, Week 6

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Score on a scale
median (inter-quartile range (Q1-Q3))	-1.0 (-1.0 to 0.0)	-1.0 (-2.0 to 0.0)	-1.0 (-2.0 to 0.0)

Etro vs. Placebo: MCS Rectal Bleeding at Week 6

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.4434 ^[20]

Method

Rank ANCOVA

Confidence interval

Notes
[20] - p-value has been adjusted for multiplicity.

Etro vs. Ada.: MCS Rectal Bleeding at Week 6

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.3374 ^[21]

Method

Rank ANCOVA

Confidence interval

Notes
[21] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Change from Baseline in MCS Stool Frequency Subscore at Week 6

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End point title

Change from Baseline in MCS Stool Frequency Subscore at Week 6

End point description

Stool frequency data were collected via the participant’s diaries and each day a participant provided a score from 0 to 3 according to the following definitions: 0 = normal number of stools; 1 = 1 to 2 more stools than normal; 2 = 3 to 4 more stools than normal; 3 = 5 or more stools than normal. The Mayo Clinic Score (MCS) stool frequency subscore was calculated as the average of three days daily diary scores closest to anchor dates at baseline and post-baseline. The data was considered non-parametric and was reported using RANK analysis of covariance (ANCOVA). Participants were stratified by concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening (MCS ≤9/MCS ≥10); the model adjusted for these stratification factors along with the baseline stool frequency (SF) subscore.

End point type

Secondary

End point timeframe

Baseline, Week 6

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Score on a scale
median (inter-quartile range (Q1-Q3))	0.0 (-1.0 to 0.0)	-1.0 (-2.0 to 0.0)	-1.0 (-2.0 to 0.0)

Etro vs. Placebo: MCS Stool Frequency at Week 6

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

216

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.4434 ^[22]

Method

Rank ANCOVA

Confidence interval

Notes
[22] - p-value has been adjusted for multiplicity.

Etro vs. Ada.: MCS Stool Frequency at Week 6

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

286

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.6367 ^[23]

Method

Rank ANCOVA

Confidence interval

Notes
[23] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Change From Baseline in Ulcerative Colitis (UC) Bowel Movement Signs and Symptoms at Week 10, as Assessed by UC Patient-Reported Outcome Signs and Symptoms (UC-PRO/SS)

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End point title

Change From Baseline in Ulcerative Colitis (UC) Bowel Movement Signs and Symptoms at Week 10, as Assessed by UC Patient-Reported Outcome Signs and Symptoms (UC-PRO/SS)

End point description

The UC-PRO/SS questionnaire was collected in the e-diary and completed by participants for at least 9 to 12 consecutive days prior to a study visit. The bowel movement domain score ranges from 0 to 27, with a higher score indicating a worse disease state. The most recent 7 daily scores available (not including the visit) were selected for the calculation of the visit score. For each item in the questionnaire, a score was calculated for a visit by taking the average of the selected daily scores. The domain score for a visit was calculated as the sum of the averaged items for each question. A Mixed Model for Repeated Measures (MMRM) analysis of the data included the fixed categorical effects of treatment, visit, study stratification factors, and treatment-by-visit interaction, and the continuous covariates of the baseline UC-PRO/SS domain and baseline UC-PRO/SS domain-by-visit interaction. An unstructured covariance matrix was used to model the within-patient errors within the MMRM.

End point type

Secondary

End point timeframe

Baseline, Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	50 ^[24]	106 ^[25]	117 ^[26]
Units: Score on a scale
least squares mean (standard error)	-5.5 ± 0.7	-5.7 ± 0.5	-6.2 ± 0.5

Notes
[24] - Only subjects with baseline and at least 1 post-baseline result were included.
[25] - Only subjects with baseline and at least 1 post-baseline result were included.
[26] - Only subjects with baseline and at least 1 post-baseline result were included.

Etro vs. Placebo: UC Bowel Movement SS at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

167

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.3708 ^[27]

Method

Mixed Model for Repeated Measures

Parameter type

Mean difference (net)

Point estimate

-0.7

Confidence interval

level

95%

sides

2-sided

lower limit

-2.4

upper limit

0.9

Notes
[27] - Nominal p-value; it has not been adjusted for multiplicity.

Etro vs. Ada.: UC Bowel Movement SS at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

223

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.4477 ^[28]

Method

Mixed Model for Repeated Measures

Parameter type

Mean difference (net)

Point estimate

-0.5

Confidence interval

level

95%

sides

2-sided

lower limit

-1.8

upper limit

0.8

Notes
[28] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Change From Baseline in UC Functional Symptoms at Week 10, as Assessed by UC-PRO/SS

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End point title

Change From Baseline in UC Functional Symptoms at Week 10, as Assessed by UC-PRO/SS

End point description

The UC-PRO/SS questionnaire was collected in the e-diary and completed by participants for at least 9 to 12 consecutive days prior to a study visit. The functional symptoms domain score ranges from 0 to 12, with a higher score indicating a worse disease state. The most recent 7 daily scores available (not including the visit) were selected for the calculation of the visit score. For each item in the questionnaire, a score was calculated for a visit by taking the average of the selected daily scores. The domain score for a visit was calculated as the sum of the averaged items for each question. A Mixed Model for Repeated Measures (MMRM) analysis of the data included the fixed categorical effects of treatment, visit, study stratification factors, and treatment-by-visit interaction, and the continuous covariates of the baseline UC-PRO/SS domain and baseline UC-PRO/SS domain-by-visit interaction. An unstructured covariance matrix was used to model the within-patient errors in the MMRM.

End point type

Secondary

End point timeframe

Baseline, Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	50 ^[29]	106 ^[30]	117 ^[31]
Units: Score on a scale
least squares mean (standard error)	-1.7 ± 0.3	-1.5 ± 0.2	-1.9 ± 0.2

Notes
[29] - Only subjects with baseline and at least 1 post-baseline result were included.
[30] - Only subjects with baseline and at least 1 post-baseline result were included.
[31] - Only subjects with baseline and at least 1 post-baseline result were included.

Etro vs. Ada.: UC Functional SS at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

223

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.1253 ^[32]

Method

Mixed Model for Repeated Measures

Parameter type

Mean difference (net)

Point estimate

-0.4

Confidence interval

level

95%

sides

2-sided

lower limit

-1

upper limit

0.1

Notes
[32] - Nominal p-value; it has not been adjusted for multiplicity.

Etro vs. Placebo: UC Functional SS at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

167

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.6356 ^[33]

Method

Mixed Model for Repeated Measures

Parameter type

Mean difference (net)

Point estimate

-0.2

Confidence interval

level

95%

sides

2-sided

lower limit

-0.9

upper limit

0.5

Notes
[33] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Change From Baseline in Health-Related Quality of Life at Week 10, as Assessed by the Total Inflammatory Bowel Disease Questionnaire (IBDQ) Score

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End point title

Change From Baseline in Health-Related Quality of Life at Week 10, as Assessed by the Total Inflammatory Bowel Disease Questionnaire (IBDQ) Score

End point description

The IBDQ is a 32-item questionnaire containing four domains: bowel symptoms (10 items), systemic symptoms (5 items), emotional function (12 items), and social function (5 items). An overall total IBDQ score was computed by summing the individual 32-item scores. The range for the IBDQ total score is 32 to 224, with higher scores denoting better health-related quality of life. The unadjusted mean and standard deviation for each study arm are reported. The change from baseline in the IBDQ score was analyzed using an ANCOVA model taking the stratification factors used at randomization into account (concomitant treatment with corticosteroids or immunosuppressants at randomization and disease activity measured during screening [MCS ≤9/MCS ≥10]), and the baseline IBDQ score used as a covariate.

End point type

Secondary

End point timeframe

Baseline, Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	63 ^[34]	127 ^[35]	124 ^[36]
Units: Score on a scale
arithmetic mean (standard deviation)	38.4 ± 35.7	39.2 ± 32.8	39.8 ± 35.3

Notes
[34] - Only subjects with baseline and at least 1 post-baseline result were included.
[35] - Only subjects with baseline and at least 1 post-baseline result were included.
[36] - Only subjects with baseline and at least 1 post-baseline result were included.

Etro vs. Placebo: IBDQ Change at Week 10

Statistical analysis description

Comparison groups

Placebo v Etrolizumab

Number of subjects included in analysis

187

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.7919 ^[37]

Method

ANCOVA

Parameter type

Difference in Adjusted Means

Point estimate

1.3

Confidence interval

level

95%

sides

2-sided

lower limit

-8.3

upper limit

10.8

Notes
[37] - Nominal p-value; it has not been adjusted for multiplicity.

Etro vs. Ada.: IBDQ Change at Week 10

Statistical analysis description

Comparison groups

Adalimumab v Etrolizumab

Number of subjects included in analysis

251

Analysis specification

Pre-specified

Analysis type

superiority

P-value

= 0.8327 ^[38]

Method

ANCOVA

Parameter type

Difference in Adjusted Means

Point estimate

-0.8

Confidence interval

level

95%

sides

2-sided

lower limit

-8.7

upper limit

Notes
[38] - Nominal p-value; it has not been adjusted for multiplicity.

Secondary: Pharmacokinetics of Etrolizumab: Serum Concentration

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End point title

Pharmacokinetics of Etrolizumab: Serum Concentration ^[39]

End point description

Serum concentrations of etrolizumab were evaluated at the primary endpoint visit (Week 10) and the secondary endpoint visit (Week 14). Both time points were two weeks after the most recent dose.

End point type

Secondary

End point timeframe

Weeks 10 and 14

Notes
[39] - The end point is not reporting statistics for all the arms in the baseline period. It is expected all the baseline period arms will be reported on when providing values for an end point on the baseline period.
Justification: The PK outcome measure of etrolizumab serum concentration was only assessed for those who had received treatment with etrolizumab.

End point values	Etrolizumab
Number of subjects analysed	143
Units: micrograms per millilitre (μg/mL)
arithmetic mean (standard deviation)
Week 10 (n = 142)	13.0 ± 5.84
Week 14 (n = 12)	17.1 ± 8.10

No statistical analyses for this end point

Secondary: Number of Participants With at Least One Adverse Event by Severity, According to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0 (NCI CTCAE v4.0)

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End point title

Number of Participants With at Least One Adverse Event by Severity, According to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0 (NCI CTCAE v4.0)

End point description

An adverse event (AE) is any untoward medical occurrence in a clinical investigation in which a patient is administered a pharmaceutical product, regardless of causal attribution. The investigator independently assessed the severity and seriousness of each recorded AE. The AE severity grading scale for the NCI CTCAE v4.0 was used for assessing severity; any AE not specifically listed was rated according to the following grading scale from 1 to 5: 1 = mild, 2 = moderate, 3 = severe, 4 = life-threatening, 5 = death. AEs of special interest included: elevated AST/ALT in combination with either elevated bilirubin or clinical jaundice; suspected transmission of infectious agent by the study drug; anaphylactic, anaphylactoid and systemic hypersensitivity reactions; and neurological signs, symptoms, and AEs that may suggest possible progressive multifocal leukoencephalopathy (PML).

End point type

Secondary

End point timeframe

From Baseline until the end of study (up to 26 weeks)

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Participants
Any Adverse Event (AE)	26	61	50
AE with Fatal Outcome	0	0	1
Serious AE	2	3	8
AE Leading to Study Treatment Discontinuation	0	2	2
AE Leading to Dose Interruption	0	1	3
Related AE	4	14	10
AE by Worst Severity, Grade 1	11	33	21
AE by Worst Severity, Grade 2	13	22	18
AE by Worst Severity, Grade 3	2	6	9
AE by Worst Severity, Grade 4	0	0	1
AE by Worst Severity, Grade 5	0	0	1
Any AEs of Special Interest	0	0	0
Confirmed PML	0	0	0
Infections	7	17	15
Serious Infections	2	0	2
Gastrointestinal Infections	1	0	1
Opportunistic Infections	0	0	0
Malignancies	0	0	0
Injection Site Reactions	0	4	1

No statistical analyses for this end point

Secondary: Number of Participants by Marked Laboratory Abnormality Status for Hematology Parameters as a Shift Table from Baseline to Week 10

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End point title

Number of Participants by Marked Laboratory Abnormality Status for Hematology Parameters as a Shift Table from Baseline to Week 10

End point description

Laboratory tests for hematology parameters were performed and values were compared with the Roche marked reference range. A marked abnormality was defined as a test result that was outside of the Roche marked reference range (labelled as 'High' or 'Low') and represented a clinically significant change from baseline. Not every laboratory abnormality qualified as an adverse event. A laboratory test result must have been reported as an adverse event if it met any of the following criteria: was accompanied by clinical symptoms; resulted in a change in study treatment or a medical intervention; or was clinically significant in the investigator's judgment. The results are presented as a shift from the baseline status to the Week 10 status. Baseline was defined as the last available assessment prior to first receipt of study drug. The 'missing' status only included participants with missing post-baseline values given they had a result at baseline. Abs = absolute count; Ery. = erythrocyte

End point type

Secondary

End point timeframe

From Baseline up to Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Participants
Eosinophils Abs - Normal to Normal	66	130	130
Eosinophils Abs - Normal to High	0	0	1
Eosinophils Abs - Normal to Missing	6	11	9
Eosinophils Abs - High to Normal	0	1	4
Hematocrit - Low to Low	0	0	2
Hematocrit - Low to Normal	0	5	3
Hematocrit - Normal to Low	3	1	2
Hematocrit - Normal to Normal	63	122	124
Hematocrit - Normal to High	0	1	0
Hematocrit - Normal to Missing	6	13	12
Hematocrit - High to Normal	0	0	1
Hemoglobin - Low to Low	4	15	11
Hemoglobin - Low to Normal	4	5	9
Hemoglobin - Low to Missing	2	0	1
Hemoglobin - Normal to Low	6	2	5
Hemoglobin - Normal to Normal	52	109	110
Hemoglobin - Normal to Missing	4	11	8
Lymphocytes Abs - Low to Low	0	0	2
Lymphocytes Abs - Low to Normal	1	3	7
Lymphocytes Abs - Normal to Low	1	2	1
Lymphocytes Abs - Normal to Normal	64	126	125
Lymphocytes Abs - Normal to Missing	6	11	9
Ery. Mean Corpuscular Volume - Normal to Normal	66	129	132
Ery. Mean Corpuscular Volume - Normal to Missing	6	13	12
Neutrophils, Total, Abs - Low to Normal	3	1	2
Neutrophils, Total, Abs - Normal to Low	1	5	0
Neutrophils, Total, Abs - Normal to Normal	58	115	118
Neutrophils, Total, Abs - Normal to High	1	3	5
Neutrophils, Total, Abs - Normal to Missing	6	11	8
Neutrophils, Total, Abs - High to Normal	2	4	9
Neutrophils, Total, Abs - High to High	1	3	1
Neutrophils, Total, Abs - High to Missing	0	0	1
Platelets - Normal to Normal	60	120	122
Platelets - Normal to High	3	5	4
Platelets - Normal to Missing	8	13	12
Platelets - High to Normal	1	0	4
Platelets - High to High	0	4	1
White Blood Cell Count - Low to Normal	0	0	1
White Blood Cell Count - Normal to Low	1	3	2
White Blood Cell Count - Normal to Normal	65	127	132
White Blood Cell Count - Normal to Missing	6	11	9
White Blood Cell Count - High to Normal	0	1	0

No statistical analyses for this end point

Secondary: Number of Participants by Marked Laboratory Abnormality Status for Chemistry Parameters as a Shift Table from Baseline to Week 10

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End point title

Number of Participants by Marked Laboratory Abnormality Status for Chemistry Parameters as a Shift Table from Baseline to Week 10

End point description

Laboratory tests for chemistry parameters were performed and values were compared with the Roche marked reference range. A marked abnormality was defined as a test result that was outside of the Roche marked reference range (labelled as 'High' or 'Low') and represented a clinically significant change from baseline. Not every laboratory abnormality qualified as an adverse event. A laboratory test result must have been reported as an adverse event if it met any of the following criteria: was accompanied by clinical symptoms; resulted in a change in study treatment or a medical intervention; or was clinically significant in the investigator's judgment. The results are presented as a shift from the baseline status to the Week 10 status. Baseline was defined as the last available assessment prior to first receipt of study drug. The 'missing' status only included participants with missing post-baseline values given they had a result at baseline.

End point type

Secondary

End point timeframe

From Baseline up to Week 10

End point values	Placebo	Adalimumab	Etrolizumab
Number of subjects analysed	72	142	144
Units: Participants
Albumin - Low to Low	0	3	0
Albumin - Low to Normal	0	2	1
Albumin - Normal to Low	0	1	0
Albumin - Normal to Normal	69	132	137
Albumin - Normal to Missing	3	4	6
Alkaline Phosphatase - Normal to Normal	67	139	138
Alkaline Phosphatase - Normal to High	1	0	0
Alkaline Phosphatase - Normal to Missing	3	3	6
Alkaline Phosphatase - High to High	1	0	0
Alanine Aminotransferase - Normal to Normal	68	137	138
Alanine Aminotransferase - Normal to High	1	0	0
Alanine Aminotransferase - Normal to Missing	3	4	6
Alanine Aminotransferase - High to Normal	0	1	0
Aspartate Aminotransferase - Normal to Normal	67	137	137
Aspartate Aminotransferase - Normal to High	1	0	0
Aspartate Aminotransferase - Normal to Missing	4	4	7
Aspartate Aminotransferase - High to Normal	0	1	0
Bicarbonate (CO2) - Low to Low	0	0	1
Bicarbonate (CO2) - Low to Normal	1	3	1
Bicarbonate (CO2) - Normal to Low	8	9	6
Bicarbonate (CO2) - Normal to Normal	55	118	123
Bicarbonate (CO2) - Normal to High	0	0	1
Bicarbonate (CO2) - Normal to Missing	4	5	6
Bicarbonate (CO2) - High to Normal	4	5	6
Bicarbonate (CO2) - High to High	0	1	0
Bicarbonate (CO2) - High to Missing	0	1	0
Blood Urea Nitrogen - Normal to Normal	69	138	138
Blood Urea Nitrogen - Normal to Missing	3	3	6
Blood Urea Nitrogen - High to Normal	0	1	0
Calcium - Low to Normal	0	0	1
Calcium - Normal to Normal	69	139	137
Calcium - Normal to Missing	3	3	6
Chloride - Low to Low	0	1	0
Chloride - Low to Missing	1	0	0
Chloride - Normal to Low	2	0	1
Chloride - Normal to Normal	67	137	137
Chloride - Normal to Missing	2	4	6
Creatinine - Normal to Normal	69	139	138
Creatinine - Normal to Missing	3	3	6
Direct Bilirubin - Normal to Normal	68	134	134
Direct Bilirubin - Normal to Missing	4	8	10
Potassium - Normal to Normal	69	139	137
Potassium - Normal to Missing	3	3	7
Sodium - Normal to Normal	68	139	137
Sodium - Normal to High	1	0	1
Sodium - Normal to Missing	2	3	6
Sodium - High to Missing	1	0	0
Total Bilirubin - Normal to Normal	68	136	137
Total Bilirubin - Normal to High	1	2	1
Total Bilirubin - Normal to Missing	3	4	6
Protein, Total - Low to Normal	0	1	1
Protein, Total - Normal to Low	0	1	0
Protein, Total - Normal to Normal	67	132	136
Protein, Total - Normal to High	2	5	0
Protein, Total - Normal to Missing	3	3	6
Protein, Total - High to High	0	0	1

No statistical analyses for this end point

Secondary: Number of Participants With Anti-Drug Antibodies (ADAs) to Etrolizumab at Baseline and Anytime Post-Baseline

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End point title

Number of Participants With Anti-Drug Antibodies (ADAs) to Etrolizumab at Baseline and Anytime Post-Baseline ^[40]

End point description

Anti-drug antibody (ADA) serum samples were collected from participants and analyzed using validated assays. Participants were considered to be ADA positive post-baseline if they were ADA negative or had missing data at baseline, but developed an ADA response following etrolizumab drug exposure (treatment-induced ADA response), or if they were ADA positive at baseline and the titer of one or more post-baseline samples was at least 0.60 titer units greater than the titer of the baseline sample (treatment-enhanced ADA response). Participants were considered to be ADA negative if they were ADA negative or had missing data at baseline and all post-baseline samples were negative, or if they were ADA positive at baseline but did not have any post-baseline samples with a titer that was at least 0.60 titer unit greater than the titer of the baseline sample (treatment unaffected).

End point type

Secondary

End point timeframe

Pre-dose (0 hour) on Day 1 and Week 4, Week 10, Week 14, and early termination/end of safety follow-up (up to 26 weeks)

Notes
[40] - The end point is not reporting statistics for all the arms in the baseline period. It is expected all the baseline period arms will be reported on when providing values for an end point on the baseline period.
Justification: The immunogenicity outcome measure of ADAs to etrolizumab at baseline and post-baseline was only assessed for those who had received treatment with etrolizumab.

End point values	Etrolizumab
Number of subjects analysed	144
Units: Participants
Positive for ADAs at Baseline (BL)	6
Negative for ADAs at BL	138
Post-BL: Positive for Treatment Emergent ADAs	27
Post-BL ADA Positive: Treatment-Induced ADAs	27
Post-BL ADA Positive: Treatment-Enhanced ADAs	0
Post-BL: Negative for Treatment Emergent ADAs	117
Post-BL ADA Negative: Treatment Unaffected	6

No statistical analyses for this end point

Adverse events

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Timeframe for reporting adverse events

From Baseline until the end of study (up to 26 weeks)

Assessment type

Systematic

Dictionary name

MedDRA

Dictionary version

23.0

Reporting group title

Placebo

Reporting group description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive placebo matching to etrolizumab subcutaneously (SC) once every 4 weeks (Q4W) up to Week 12 (Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]) and placebo matching to adalimumab SC once every 2 weeks (Q2W) up to Week 8 (Weeks 0 [Day 1], 2, 4, 6, and 8).

Reporting group title

Etrolizumab

Reporting group description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive etrolizumab 105 mg subcutaneously (SC) Q4W up to Week 12 (Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]) and placebo matching to adalimumab SC Q2W up to Week 8 (Weeks 0 [Day 1], 2, 4, 6, and 8).

Reporting group title

Adalimumab

Reporting group description

The double-blinded treatment period consisted of a 10-week induction period and an additional 4-week treatment period for participants who met the definition of clinical remission at Week 10. Participants with moderate-to-severe ulcerative colitis who were naive to TNF inhibitors were randomized to this arm to receive adalimumab subcutaneously (SC) Q2W up to Week 8 (160 mg Week 0 [Day 1], 80 mg SC Week 2, 40 mg SC Weeks 4, 6, and 8) and placebo matching to etrolizumab SC Q4W up to Week 12 (Weeks 0 [Day 1], 4, 8, and 12 [clinical remitters only]).

Serious adverse events	Placebo	Etrolizumab	Adalimumab
Total subjects affected by serious adverse events
subjects affected / exposed	2 / 72 (2.78%)	8 / 144 (5.56%)	3 / 142 (2.11%)
number of deaths (all causes)	0	1	0
number of deaths resulting from adverse events
Injury, poisoning and procedural complications
Procedural intestinal perforation
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Vascular disorders
Deep vein thrombosis
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Cardiac disorders
Cardiac arrest
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 1	0 / 0
Blood and lymphatic system disorders
Anaemia
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Gastrointestinal disorders
Colitis ulcerative
subjects affected / exposed	0 / 72 (0.00%)	2 / 144 (1.39%)	3 / 142 (2.11%)
occurrences causally related to treatment / all	0 / 0	0 / 2	0 / 3
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Reproductive system and breast disorders
Prostatitis
subjects affected / exposed	1 / 72 (1.39%)	0 / 144 (0.00%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 1	0 / 0	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Hepatobiliary disorders
Cholelithiasis
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Respiratory, thoracic and mediastinal disorders
Dyspnoea
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Infections and infestations
Eye infection toxoplasmal
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	1 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Pneumonia
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Pneumonia bacterial
subjects affected / exposed	1 / 72 (1.39%)	0 / 144 (0.00%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	1 / 1	0 / 0	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Pyelonephritis acute
subjects affected / exposed	1 / 72 (1.39%)	0 / 144 (0.00%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 1	0 / 0	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0
Metabolism and nutrition disorders
Hypoalbuminaemia
subjects affected / exposed	0 / 72 (0.00%)	1 / 144 (0.69%)	0 / 142 (0.00%)
occurrences causally related to treatment / all	0 / 0	0 / 1	0 / 0
deaths causally related to treatment / all	0 / 0	0 / 0	0 / 0

Frequency threshold for reporting non-serious adverse events: 5%

Non-serious adverse events	Placebo	Etrolizumab	Adalimumab
Total subjects affected by non serious adverse events
subjects affected / exposed	7 / 72 (9.72%)	6 / 144 (4.17%)	17 / 142 (11.97%)
Nervous system disorders
Headache
subjects affected / exposed	3 / 72 (4.17%)	1 / 144 (0.69%)	9 / 142 (6.34%)
occurrences all number	4	1	15
Gastrointestinal disorders
Colitis ulcerative
subjects affected / exposed	4 / 72 (5.56%)	5 / 144 (3.47%)	8 / 142 (5.63%)
occurrences all number	4	5	9

More information

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Were there any global substantial amendments to the protocol? Yes

08 Apr 2014

Protocol Version 2: The protocol was amended to reflect program level recommendations from the US FDA as follows: -The definition of moderate to severe ulcerative colitis (UC) was updated to include stool frequency subscore of ≥1. -Ulcerative Colitis Disease Activity Assessments section was modified to include that: 1) given the potential for increased rectal bleeding following endoscopic procedures, rectal bleeding MCS will be derived prior to endoscopy; 2) post-baseline endoscopy should be performed on the same day as the study visit instead of 4 days prior to the visit; 3) each segment, instead of the worst affected segment, of the colon up to the splenic flexure (rectum, sigmoid, and descending colon) will be assigned an endoscopic subscore and the score from the worst affected segment up to the splenic flexure is to be used for the MCS calculation; 4) any discrepancy between the endoscopic subscore obtained by the local versus central readers will require a third adjudication read by a different central reader.

23 Jul 2014

Protocol Version 3: The protocol was amended to simplify the study design and to facilitate early access to open-label etrolizumab to eligible patients as follows: -Administration of adalimumab/adalimumab placebo at Weeks 10 and 12 was removed for all arms (for earlier washout) to facilitate earlier entry into the Open-Label Extension (OLE Part 1) of the OLE-SM (Open-Label Extension-Safety Monitoring) study (Study GA28951). Table “Study Drug Administration Schema” was updated accordingly. -Only patients achieving clinical remission at Week 10 will progress to Weeks 12 and 14 of the study to confirm maintenance of induction. Patients not achieving clinical remission at Week 10 should remain in the blinded study until Week 12 (to enable adalimumab washout) at which time they may enroll in the OLE.

18 Sep 2015

Protocol Version 4: The protocol was amended following FDA response to a type C request as follows: -Previously, the FDA had mandated a discontinuation of immunosuppressant therapy after Week 10 because of hypothetical risk of PML, resulting in distinct instructions regarding immunosuppressant use in different countries in the protocol. However, the Sponsor recently received agreement from the FDA to amend the global protocol GA28948 to instruct patients to continue their stable, baseline dose of immunosuppressants to the end of study treatment with dose reduction or discontinuation if patient experiences an immunosuppressant-related toxicity. Consequently the protocol was amended to allow patients to continue with immunosuppressant use from baseline to the end of study treatment (with dose reduction or discontinuation of immunosuppressant use permitted in the event of toxicity) in United States. -Following FDA feedback, inclusion criterion for patients at U.S. sites was amended to allow patients who had had an inadequate response to either immunosuppressants and/or corticosteroids to be eligible for the study rather than the previous requirement for failure to immunosuppressants with or without failure to corticosteroids. These two changes aligned United States with the rest of world regarding immunosuppressant use during the study and eligibility requirements for prior immunosuppressant/corticosteroid usage. Contents that indicated the use of immunosuppressants in the United States had to stop at Week 10 was removed.

18 Dec 2016

Protocol Version 5: The protocol was amended to update and align the safety section with information regarding potential risks for etrolizumab in the current Etrolizumab Investigator’s Brochure, Version 10, and to account for a change in adalimumab formulation, as follows: -The protocol was amended to include the use of the new formulation of adalimumab as needed, when supplies of the current formulation (40 mg [0.8mL]) could no longer be procured. The new formulation consisted of 40 mg (0.4 mL) of adalimumab provided in a single-use, 1-mL, glass prefilled syringe with a fixed 29-gauge ½-inch needle. The efficacy, safety, and tolerability profile of the new formulation was comparable to that of the formulation currently in use (40 mg [0.8 mL]). -The protocol was updated and added to include potential hepatic effects to be in line with the safety profile of other anti-integrins, including vedolizumab, for which hepatic adverse events were reported. Although no clear hepatic safety signals emerged to date with etrolizumab, this potential risk was considered to be applicable across the anti-integrin class and would be evaluated in all etrolizumab studies.

30 Aug 2017

Protocol Version 6: The protocol was amended to enhance recruitment by reducing the complexity of the protocol, particularly at the time of screening and re-screening, as follows: -The requirement for obtaining Medical Monitor approval for extension of the screening period from 28 to 35 days was eliminated to accommodate logistic delays that might arise during the screening period and decrease site burden associated with placing approval requests. The screening window would not be extended beyond 35 days under any circumstances. -The time qualification for derivation of Mayo Clinic Score (MCS) baseline stool frequency and rectal bleeding subscores was redefined to include subscores obtained within 22 days prior to randomization (Day 1). Post-endoscopy subscores might be used, starting 2 days after the screening endoscopy, but only in cases where there were insufficient e-diary data to calculate these subscores prior to the bowel preparation day.

25 Oct 2018

Protocol Version 7: The protocol was amended primarily to reflect changes in efficacy endpoints. The changes would not impact study conduct at the site level. These changes are as follows: -To assess the onset of action of etrolizumab, secondary efficacy endpoints of change in Mayo Clinic Score (MCS) rectal bleeding and stool frequency subscores from baseline to Week 6 were added. -The secondary efficacy objective to evaluate colonic mucosal alphaE integrin concentration as a biomarker was expanded and would be evaluated as an exploratory efficacy endpoint to support additional biomarker candidate evaluations in the pivotal placebo-controlled studies within the etrolizumab Phase III Program. -Derivation of the MCS endoscopic subscore at post-baseline timepoints was amended to be consistent with emerging normative standards of endoscopic assessment in clinical trials (Sandborn et al. 2017). The sigmoid colon MCS endoscopic subscore would be used (rather than the score from the worst affected segment, i.e., rectum, sigmoid colon, or descending colon) if the baseline sigmoid colon MCS endoscopic subscore was 2-3. The sigmoid colon MCS endoscopic subscore was considered to be more reliable in assessing earlier treatment response.

15 Mar 2019

Protocol Version 8: The protocol was amended to provide further clarification and exploratory efficacy objectives was modified as follows: -Evaluation of response at Week 10, in subgroups by baseline expression levels of colonic tissue and/or peripheral blood biomarkers, was added to predict patient subgroups with a greater likelihood of responding to etrolizumab.

Were there any global interruptions to the trial? No

Limitations of the trial such as small numbers of subjects analysed or technical problems leading to unreliable data.

None reported

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Clinical trials

Trial information

Trial information

Subject disposition

Subject disposition

Baseline characteristics

Baseline characteristics

End points

End points

Primary: Percentage of Participants in Remission With Etrolizumab Compared With Placebo at Week 10, as Determined by the Mayo Clinic Score (MCS)

Primary: Percentage of Participants in Remission With Etrolizumab Compared With Placebo at Week 10, as Determined by the Mayo Clinic Score (MCS)

Secondary: Percentage of Participants in Remission With Etrolizumab Compared With Adalimumab at Week 10, as Determined by the MCS

Secondary: Percentage of Participants in Remission With Etrolizumab Compared With Adalimumab at Week 10, as Determined by the MCS

Secondary: Percentage of Participants in Clinical Remission at Week 10, as Determined by the MCS

Secondary: Percentage of Participants in Clinical Remission at Week 10, as Determined by the MCS

Secondary: Percentage of Participants With Clinical Response at Week 10, as Determined by the MCS

Secondary: Percentage of Participants With Clinical Response at Week 10, as Determined by the MCS

Secondary: Percentage of Participants With Improvement in Endoscopic Appearance of the Mucosa at Week 10, as Determined by the MCS Endoscopy Subscore

Secondary: Percentage of Participants With Improvement in Endoscopic Appearance of the Mucosa at Week 10, as Determined by the MCS Endoscopy Subscore

Secondary: Percentage of Participants in Endoscopic Remission at Week 10, as Determined by the MCS Endoscopy Subscore

Secondary: Percentage of Participants in Endoscopic Remission at Week 10, as Determined by the MCS Endoscopy Subscore

Secondary: Percentage of Participants in Remission at Week 10 and Week 14, as Determined by the MCS

Secondary: Percentage of Participants in Remission at Week 10 and Week 14, as Determined by the MCS

Secondary: Percentage of Participants With Histologic Remission at Week 10, as Determined by the Nancy Histological Index

Secondary: Percentage of Participants With Histologic Remission at Week 10, as Determined by the Nancy Histological Index

Secondary: Change from Baseline in MCS Rectal Bleeding Subscore at Week 6

Secondary: Change from Baseline in MCS Rectal Bleeding Subscore at Week 6

Secondary: Change from Baseline in MCS Stool Frequency Subscore at Week 6

Secondary: Change from Baseline in MCS Stool Frequency Subscore at Week 6

Secondary: Change From Baseline in Ulcerative Colitis (UC) Bowel Movement Signs and Symptoms at Week 10, as Assessed by UC Patient-Reported Outcome Signs and Symptoms (UC-PRO/SS)

Secondary: Change From Baseline in Ulcerative Colitis (UC) Bowel Movement Signs and Symptoms at Week 10, as Assessed by UC Patient-Reported Outcome Signs and Symptoms (UC-PRO/SS)

Secondary: Change From Baseline in UC Functional Symptoms at Week 10, as Assessed by UC-PRO/SS

Secondary: Change From Baseline in UC Functional Symptoms at Week 10, as Assessed by UC-PRO/SS

Secondary: Change From Baseline in Health-Related Quality of Life at Week 10, as Assessed by the Total Inflammatory Bowel Disease Questionnaire (IBDQ) Score

Secondary: Change From Baseline in Health-Related Quality of Life at Week 10, as Assessed by the Total Inflammatory Bowel Disease Questionnaire (IBDQ) Score

Secondary: Pharmacokinetics of Etrolizumab: Serum Concentration

Secondary: Pharmacokinetics of Etrolizumab: Serum Concentration

Secondary: Number of Participants With at Least One Adverse Event by Severity, According to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0 (NCI CTCAE v4.0)

Secondary: Number of Participants With at Least One Adverse Event by Severity, According to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.0 (NCI CTCAE v4.0)

Secondary: Number of Participants by Marked Laboratory Abnormality Status for Hematology Parameters as a Shift Table from Baseline to Week 10

Secondary: Number of Participants by Marked Laboratory Abnormality Status for Hematology Parameters as a Shift Table from Baseline to Week 10

Secondary: Number of Participants by Marked Laboratory Abnormality Status for Chemistry Parameters as a Shift Table from Baseline to Week 10

Secondary: Number of Participants by Marked Laboratory Abnormality Status for Chemistry Parameters as a Shift Table from Baseline to Week 10

Secondary: Number of Participants With Anti-Drug Antibodies (ADAs) to Etrolizumab at Baseline and Anytime Post-Baseline

Secondary: Number of Participants With Anti-Drug Antibodies (ADAs) to Etrolizumab at Baseline and Anytime Post-Baseline

Adverse events

Adverse events

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Substantial protocol amendments (globally)

Interruptions (globally)

Limitations and caveats

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