Study to Assess Safety and Effectiveness of Branebrutinib... | NCT04186871 | Trialant
NCT04186871
Sponsor
Bristol-Myers Squibb
Status
Completed
Last Update Posted
Jan 16, 2024Actual
Enrollment
119Actual
Phase
Phase 2
Conditions
Autoimmune Disorder
Rheumatoid Arthritis
Systemic Lupus Erythematosus
Primary Sjögren's Syndrome
Interventions
branebrutinib
abatacept
branebrutinib placebo
Countries
United States
Argentina
Belgium
France
Germany
Mexico
Netherlands
Poland
Spain
United Kingdom
Protocol Section
Identification Module
NCT ID
NCT04186871
Obsolete or Duplicate NCT IDs
Not provided
Organization Study
IM014-029
Secondary IDs
ID
Type
Description
Link
2019-002205-22
EudraCT Number
Brief Title
Study to Assess Safety and Effectiveness of Branebrutinib Treatment in Participants With Active Systemic Lupus Erythematosus or Primary Sjögren's Syndrome, or Branebrutinib Treatment Followed by Open-label Abatacept Treatment in Study Participants With Active Rheumatoid Arthritis
Official Title
A Randomized, Placebo-Controlled, Double-Blind, Multicenter Study to Assess the Efficacy and Safety of Branebrutinib Treatment in Subjects With Active Systemic Lupus Erythematosus or Primary Sjögren's Syndrome, or Branebrutinib Treatment Followed by Open-label Abatacept Treatment in Subjects With Active Rheumatoid Arthritis
Acronym
Not provided
Organization
Bristol-Myers SquibbINDUSTRY
Status Module
Record Verification Date
Jan 2024
Overall Recruitment Status or Expanded Access Status
Completed
Last Known Status
Not provided
Delayed Posting
Not provided
Why Stopped
Not provided
Expanded Access Info
No
Start Date
Jan 7, 2020Actual
Primary Completion Date
Dec 5, 2022Actual
Completion Date
Dec 5, 2022Actual
First Submitted Date
Nov 28, 2019
First Submission Date that Met QC Criteria
Dec 2, 2019
First Posted Date
Dec 5, 2019Actual
Results Waived
Not provided
Results First Submitted Date
Dec 5, 2023
Results First Submitted that Met QC Criteria
Jan 12, 2024
Results First Posted Date
Jan 16, 2024Actual
Certification/Extension (aka Delayed Results) First Submitted Date
Not provided
Certification/Extension First Submitted that Passed QC Review
Not provided
Certification/Extension First Posted Date
Not provided
Last Update Submitted Date
Jan 12, 2024
Last Update Posted Date
Jan 16, 2024Actual
Sponsor/Collaborators Module
Responsible Party, by Official Title
Sponsor
Lead Sponsor
Bristol-Myers SquibbINDUSTRY
Collaborators
Not provided
Oversight Module
Has Data Monitoring Committee (DMC)
Yes
Is FDA Regulated Drug
Yes
Is FDA Regulated Device
No
Is Unapproved Device
Not provided
Pediatric Postmarket Surveillance of a Device Product
Not provided
Product Exported from US
Not provided
FDAAA801 Violation
Not provided
Description Module
Brief Summary
The purpose of this study is to evaluate the safety and effectiveness of treatment with branebrutinib treatment in participants with active systemic Lupus Erythematosus (SLE) or Primary Sjögren's Syndrome (pSS), or branebrutinib treatment followed by open-label abatacept treatment in study participants with active Rheumatoid Arthritis (RA).
Detailed Description
Not provided
Conditions Module
Conditions
Autoimmune Disorder
Rheumatoid Arthritis
Systemic Lupus Erythematosus
Primary Sjögren's Syndrome
Keywords
Not provided
Design Module
Study Type
Interventional
Number of References to an Expanded Access Study
Not provided
Expanded Access Types
Not provided
Patient Registry
Not provided
Target Follow-Up Duration
Not provided
Phases
Phase 2
Interventional Study Design
Allocation
Biospecimen
No data available
No data is available for this block.
Enrollment
119Actual
Arms/Interventions Module
Arm Groups
Label
Type
Description
Intervention Names
Systemic Lupus Erythematosus (SLE): branebrutinib
Experimental
Drug: branebrutinib
SLE: placebo
Placebo Comparator
Drug: branebrutinib placebo
Primary Sjögren's Syndrome (pSS): branebrutinib
Experimental
Drug: branebrutinib
pSS: placebo
Placebo Comparator
Drug: branebrutinib placebo
Rheumatoid Arthritis (RA): branebrutinib followed by abatacept
Experimental
Drug: branebrutinib
Drug: abatacept
RA: placebo followed by abatacept
Placebo Comparator
Drug: abatacept
Drug: branebrutinib placebo
Interventions
Name
Type
Description
Arm Group Labels
Other Names
branebrutinib
Drug
Specified dose on specified days
Primary Sjögren's Syndrome (pSS): branebrutinib
Rheumatoid Arthritis (RA): branebrutinib followed by abatacept
Outcomes Module
Primary Outcomes
Measure
Description
Time Frame
The Percent of Participants With mCLASI Response at Week 24 and Corticosteroid (CS) < 10 mg/Day at Week 20 and Week 24 - SLE
mCLASI response is defined as a decrease of ≥ 50% from baseline mCLASI activity score, in participants with a baseline mCLASI activity score ≥ 10, at Week 24. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
To be considered as meeting the second criterion, the CS (prednisone or equivalent) dose had to remain stable and ≤ 10 mg from Week 16 until Week 24.
The modified CLASI (mCLASI) is defined as the activity portions of CLASI that describe skin erythema and scale/hypertrophy and inflammation of the scalp. The percentage of patients who entered the study with a positive mCLASI activity score (≥ 10) and who achieved a ≥ 50% decrease from baseline at Week 24 is considered to likely represent a clinically meaningful improvement. The scores are calculated by simple addition based on the extent of the symptoms.
mCLASI: Modified Cutaneous Lupus Erythematosus Disease Area and Severity Index
Week 24
The Percent of Participants With Composite Response at Week 24 - pSS
Composite response is defined as the percent of participants with at least 3 of the following at Week 24:
Decrease of ≥ 1 point or 15% from baseline in the ESSPRI Total Score
Decrease of ≥ 3 points from baseline in ESSDAI score
Decrease of ≥ 25% from baseline in ocular staining score, or if normal score at baseline no change to abnormal
Increase of ≥ 25% from baseline in stimulated salivary flow
Improvement in one or more serological markers (rheumatoid factor (RF), immunoglobulin G protein (IgG), complement C3 or C4, cryoglobulin).
Week 24
Percent of Participants With ACR50 Response at Week 12 Compared to Baseline - RA
ACR50 response is defined as both improvement of 50% in the number of tender and swollen joints and a 50% improvement in 3 of the following 5 criteria:
Subject global assessment (SGA)
Physician global assessment (PGA)
Functional ability measure
Pain visual analog scale (VAS)
Erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP).
Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
Secondary Outcomes
Measure
Description
Time Frame
Change From Baseline in SLEDAI-2K Score at Week 24 - SLE
The SLEDAI-2K is a global index providing a total score of overall disease activity ranging from 0 to 105, with higher scores representing more active disease. The SLEDAI index includes 24 items divided into 9 organ systems: neurological, musculoskeletal, renal, mucocutaneous, general, heart, respiratory, vascular, and hematological. Each item is scored based on the severity of the symptom or finding, with higher scores indicating more severe disease activity. The weighted scores for each item range from 0 to 8. To calculate the SLEDAI-2K score, the scores for each of the 24 items are added together.
Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
Other Outcomes
Not provided
Eligibility Module
Eligibility Criteria
Inclusion Criteria:
Sub-study for Systemic Lupus Erythematosus (SLE)
Active SLE as defined by the Systemic Lupus Erythematosus International Collaborating Clinics (SLICC) classification
Diagnosed with SLE more than 24 weeks before screening visit
Sub-study for primary Sjögren's Syndrome (pSS)
Moderate to severe pSS, meeting ACR-EULAR classification criteria
Sub-study for active Rheumatoid Arthritis (RA)
Moderate to severe adult-onset RA
ACR global functional status class I to III
Women and men must agree to follow instructions for methods of contraception.
Exclusion Criteria:
Sub-study for SLE
Certain other autoimmune diseases and overlap syndromes
Sub-study for pSS
Certain other immune-mediated diseases, active fibromyalgia, or other medical conditions
Sub-study for RA
Diagnosis with juvenile arthritis or idiopathic arthritis before age 16
For all sub-studies:
History of any significant drug allergy
Active infection, significant concurrent medical condition, or clinically significant abnormalities
Other protocol defined inclusion/exclusion criteria could apply
Ostergaard M, Haavardsholm EA, Nowak M, Luo Y, Landis J, Fura A, Pachai C, Rotich D, Wang-Fischer Y, Carayannopoulos LN, Zammit D, Karabeber H, Wang A, Grasela DM. Efficacy and safety of branebrutinib (BMS-986195), an irreversible Bruton's tyrosine kinase inhibitor, for the treatment of rheumatoid arthritis: a phase 2a, randomised, double-blind, placebo-controlled study. Lancet Rheumatol. 2026 Jul;8(7):e539-e549. doi: 10.1016/S2665-9913(25)00374-1. Epub 2026 May 1.
Participants were enrolled concurrently for the RA, SLE, and pSS sub-studies.
Recruitment Details
Not provided
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
FG000
SLE- Placebo
Participants with systemic lupus erythematosus (SLE) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
Rheumatoid Arthritis (RA): branebrutinib followed by abatacept
branebrutinib placebo
Drug
Specified dose on specified days
RA: placebo followed by abatacept
SLE: placebo
pSS: placebo
Week 12
Week 24
Percent of Participants With BICLA Response at Week 24 - SLE
BILAG-based composite lupus assessment (BICLA) response is defined as:
At least one gradation of improvement in baseline BILAG scores in all body systems with moderate or severe disease activity at entry
No new BILAG A or more than one new BILAG B scores
No worsening of total SLEDAI score from baseline
No significant deterioration (< 10%) in PGA and
No treatment failure (initiation of nonprotocol treatment).
BILAG scores: A (severe disease), B (moderate), C (mild), or D (no activity). Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
Week 24
Change From Baseline in DAS28-CRP at Week 12 - RA
The Disease Activity Score-28-C-Reactive Protein (DAS28CRP) is a composite outcome assessment that measures: 1) How many joints in the hands, wrists, elbows, shoulders, and knees are swollen and/or tender over a total of 28, 2) CRP in the blood to measure the degree of inflammation, and 3) SGA of disease activity.
DAS28-CRP scores range from 1.0 to 9.4, where lower scores indicate less disease activity. The results are combined to produce the DAS28-CRP score, which correlates with the extent of disease activity:
A negative change from baseline in DAS28-CRP indicates an improvement. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
Week 12
Change From Baseline in DAS28-ESR at Week 12 - RA
The Disease Activity Score Erythrocyte Sedimentation Rate - DAS28ESR is a composite outcome assessment that measures:
How many joints in the hands, wrists, elbows, shoulders, and knees are swollen and/or tender over a total of 28
ESR in the blood to measure the degree of inflammation
SGA of disease activity
DAS28-ESR scores range from 1.0 to 9.4, where lower scores indicate less disease activity. The results are combined to produce the DAS28-ESR score, which correlates with the extent of disease activity:
A negative change from baseline in DAS28-ESR indicates an improvement. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
Week 12
Change From Baseline in SDAI at Week 12- RA
The Simplified Disease Activity Index (SDAI) is the sum of the tender joint score (range 0 to 28), the swollen joint score (range 0 to 28), the subject global assessment (SGA) of disease activity (range 0 to 10 in increments of 0.5), the PGA of disease activity (range 0 to 10 in increments of 0.5), and C-reactive protein (CRP) test result. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment. A SDAI score ranges from 0 (disease remission) to 86 (high disease activity).
Week 12
Change From Baseline in CDAI at Week 12 - RA
The Clinical Disease Activity Index (CDAI) is the sum of the tender joint score (range 0 to 28), the swollen joint score (range 0 to 28), the SGA of disease activity (range 0 to 10 in increments of 0.5), and the PGA of disease activity (range 0 to 10 in increments of 0.5). Baseline values are defined as the last nonmissing value prior to the first dose of study treatment. A CDAI score ranges from 0 to 76.
Participants with systemic lupus erythematosus (SLE) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
FG002
pSS- Placebo
Participants with primary Sjögren's syndrome (pSS) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
FG003
pSS- Branebrutinib
Participants with primary Sjögren's syndrome (pSS) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
FG004
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
FG005
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
FG0005 subjects
FG00115 subjects
FG0024 subjects
FG00310 subjects
FG00421 subjects
FG00564 subjects
Double Blind Period
FG0005 subjects
FG00115 subjects
FG0024 subjects
FG00310 subjects
FG00421 subjects
FG00564 subjects
Open Label Period
The Open Label Period was available to RA sub-study participants only.
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG00420 subjects
FG00561 subjects
COMPLETED
FG0003 subjects
FG00111 subjects
FG0024 subjects
FG0039 subjects
FG00420 subjects
FG00558 subjects
NOT COMPLETED
FG0002 subjects
FG0014 subjects
FG0020 subjects
FG0031 subjects
FG0041 subjects
FG0056 subjects
Type
Comment
Reasons
Lack of Efficacy
FG0000 subjects
FG0011 subjects
FG0020 subjects
FG0030 subjects
FG0041 subjects
FG0051 subjects
Adverse Event
FG0001 subjects
FG0011 subjects
FG0020 subjects
FG0030 subjects
FG004
Study terminated by sponsor
FG0001 subjects
FG0012 subjects
FG0020 subjects
FG0031 subjects
FG004
Other reasons
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Withdrawal by Subject
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Lost to Follow-up
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
BG000
SLE- Placebo
Participants with systemic lupus erythematosus (SLE) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
BG001
SLE- Branebrutinib
Participants with systemic lupus erythematosus (SLE) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
BG002
pSS- Placebo
Participants with primary Sjögren's syndrome (pSS) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
BG003
pSS- Branebrutinib
Participants with primary Sjögren's syndrome (pSS) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
BG004
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
BG005
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
BG006
Total
Total of all reporting groups
Denominators
Units
Counts
Participants
BG0005
BG00115
BG0024
BG00310
BG00421
BG00564
BG006119
Baseline Measures
Title
Description
Population Description
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Denominator Units Selected
Denominators
Classes
Age, Continuous
Mean
Standard Deviation
Years
Title
Denominators
Categories
Title
Measurements
BG00047.6± 10.99
BG00144.2± 12.91
BG00247.8± 4.19
BG003
Sex: Female, Male
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Female
BG0005
BG00114
BG002
Ethnicity (NIH/OMB)
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Hispanic or Latino
BG0003
BG0019
BG002
Race/Ethnicity, Customized
Count of Participants
Participants
Title
Denominators
Categories
Asian - Non-Japanese
Title
Measurements
Asian - Non-Japanese
BG0000
BG0010
BG002
Type
Title
Description
Population Description
Reporting Status
Anticipated Posting Date
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Time Frame
Units Analyzed
Denominator Units Selected
Arm/Group Information
Denominators
Classes
Analyses
Primary
The Percent of Participants With mCLASI Response at Week 24 and Corticosteroid (CS) < 10 mg/Day at Week 20 and Week 24 - SLE
mCLASI response is defined as a decrease of ≥ 50% from baseline mCLASI activity score, in participants with a baseline mCLASI activity score ≥ 10, at Week 24. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
To be considered as meeting the second criterion, the CS (prednisone or equivalent) dose had to remain stable and ≤ 10 mg from Week 16 until Week 24.
The modified CLASI (mCLASI) is defined as the activity portions of CLASI that describe skin erythema and scale/hypertrophy and inflammation of the scalp. The percentage of patients who entered the study with a positive mCLASI activity score (≥ 10) and who achieved a ≥ 50% decrease from baseline at Week 24 is considered to likely represent a clinically meaningful improvement. The scores are calculated by simple addition based on the extent of the symptoms.
mCLASI: Modified Cutaneous Lupus Erythematosus Disease Area and Severity Index
All treated participants with a baseline mCLASI activity score ≥ 10 at Week 24 (Prespecified for participants in the SLE cohort only).
Posted
Number
95% Confidence Interval
Percentage of participants
Week 24
ID
Title
Description
OG000
SLE- Placebo
Participants with systemic lupus erythematosus (SLE) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
OG001
SLE- Branebrutinib
Participants with systemic lupus erythematosus (SLE) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
Units
Counts
Participants
OG0005
OG00115
Title
Denominators
Categories
Title
Measurements
OG00060.0(17.1 to 100)
OG00133.3(9.5 to 57.2)
Group IDs
Group Description
Statistical Method
Statistical Comment
P-Value
P-Value Comment
Parameter Type
Parameter Value
Dispersion Type
Dispersion Value
Confidence Interval Sides
Confidence Interval %
CI Lower Limit
CI Upper Limit
CI Lower Limit Comment
CI Upper Limit Comment
Estimate Comment
Tested Non-Inferiority
Non-Inferiority Type
Non-Inferiority Comment
Other Analysis Description
OG000
OG001
Response Difference
-27.8
2-Sided
95
-77.5
21.9
Superiority
RESPONSE DIFFERENCE (95% CI) VS PLACEBO
OG000
OG001
Cochran-Mantel-Haenszel
Secondary
Change From Baseline in SLEDAI-2K Score at Week 24 - SLE
The SLEDAI-2K is a global index providing a total score of overall disease activity ranging from 0 to 105, with higher scores representing more active disease. The SLEDAI index includes 24 items divided into 9 organ systems: neurological, musculoskeletal, renal, mucocutaneous, general, heart, respiratory, vascular, and hematological. Each item is scored based on the severity of the symptom or finding, with higher scores indicating more severe disease activity. The weighted scores for each item range from 0 to 8. To calculate the SLEDAI-2K score, the scores for each of the 24 items are added together.
Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
All Treated Participants with week 24 measurements (Prespecified for participants in the SLE cohort only).
Posted
Mean
Standard Deviation
Change in "score on a scale"
Week 24
ID
Title
Description
OG000
SLE- Placebo
Participants with systemic lupus erythematosus (SLE) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
OG001
SLE- Branebrutinib
Participants with systemic lupus erythematosus (SLE) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
Secondary
Percent of Participants With BICLA Response at Week 24 - SLE
BILAG-based composite lupus assessment (BICLA) response is defined as:
At least one gradation of improvement in baseline BILAG scores in all body systems with moderate or severe disease activity at entry
No new BILAG A or more than one new BILAG B scores
No worsening of total SLEDAI score from baseline
No significant deterioration (< 10%) in PGA and
No treatment failure (initiation of nonprotocol treatment).
BILAG scores: A (severe disease), B (moderate), C (mild), or D (no activity). Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
All Treated Participants (Prespecified for participants in the SLE cohort only).
Posted
Number
95% Confidence Interval
Percent of participants
Week 24
ID
Title
Description
OG000
SLE- Placebo
Participants with systemic lupus erythematosus (SLE) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
OG001
SLE- Branebrutinib
Participants with systemic lupus erythematosus (SLE) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
Primary
The Percent of Participants With Composite Response at Week 24 - pSS
Composite response is defined as the percent of participants with at least 3 of the following at Week 24:
Decrease of ≥ 1 point or 15% from baseline in the ESSPRI Total Score
Decrease of ≥ 3 points from baseline in ESSDAI score
Decrease of ≥ 25% from baseline in ocular staining score, or if normal score at baseline no change to abnormal
Increase of ≥ 25% from baseline in stimulated salivary flow
Improvement in one or more serological markers (rheumatoid factor (RF), immunoglobulin G protein (IgG), complement C3 or C4, cryoglobulin).
All Treated Participants (Prespecified for participants in the pSS cohort only).
Posted
Number
95% Confidence Interval
Percent of Participants
Week 24
ID
Title
Description
OG000
pSS- Placebo
Participants with primary Sjögren's syndrome (pSS) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
OG001
pSS- Branebrutinib
Participants with primary Sjögren's syndrome (pSS) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
Units
Counts
Primary
Percent of Participants With ACR50 Response at Week 12 Compared to Baseline - RA
ACR50 response is defined as both improvement of 50% in the number of tender and swollen joints and a 50% improvement in 3 of the following 5 criteria:
Subject global assessment (SGA)
Physician global assessment (PGA)
Functional ability measure
Pain visual analog scale (VAS)
Erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP).
Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
All Treated Participants (Prespecified for participants in the RA cohort only).
Posted
Number
95% Confidence Interval
Percent of Participants
Week 12
ID
Title
Description
OG000
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
OG001
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
Units
Secondary
Change From Baseline in DAS28-CRP at Week 12 - RA
The Disease Activity Score-28-C-Reactive Protein (DAS28CRP) is a composite outcome assessment that measures: 1) How many joints in the hands, wrists, elbows, shoulders, and knees are swollen and/or tender over a total of 28, 2) CRP in the blood to measure the degree of inflammation, and 3) SGA of disease activity.
DAS28-CRP scores range from 1.0 to 9.4, where lower scores indicate less disease activity. The results are combined to produce the DAS28-CRP score, which correlates with the extent of disease activity:
A negative change from baseline in DAS28-CRP indicates an improvement. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
All Treated Participants with baseline and week 12 measurements (Prespecified for participants in the RA cohort only).
Posted
Mean
Standard Deviation
Score on a scale
Week 12
ID
Title
Description
OG000
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
OG001
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
Secondary
Change From Baseline in DAS28-ESR at Week 12 - RA
The Disease Activity Score Erythrocyte Sedimentation Rate - DAS28ESR is a composite outcome assessment that measures:
How many joints in the hands, wrists, elbows, shoulders, and knees are swollen and/or tender over a total of 28
ESR in the blood to measure the degree of inflammation
SGA of disease activity
DAS28-ESR scores range from 1.0 to 9.4, where lower scores indicate less disease activity. The results are combined to produce the DAS28-ESR score, which correlates with the extent of disease activity:
A negative change from baseline in DAS28-ESR indicates an improvement. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
All treated participants with baseline and week 12 measurements (Prespecified for participants in the RA cohort only).
Posted
Mean
Standard Deviation
Score on a scale
Week 12
ID
Title
Description
OG000
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
OG001
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
Secondary
Change From Baseline in SDAI at Week 12- RA
The Simplified Disease Activity Index (SDAI) is the sum of the tender joint score (range 0 to 28), the swollen joint score (range 0 to 28), the subject global assessment (SGA) of disease activity (range 0 to 10 in increments of 0.5), the PGA of disease activity (range 0 to 10 in increments of 0.5), and C-reactive protein (CRP) test result. Baseline values are defined as the last nonmissing value prior to the first dose of study treatment. A SDAI score ranges from 0 (disease remission) to 86 (high disease activity).
All treated participants with baseline and week 12 measurements (Prespecified for participants in the RA cohort only).
Posted
Mean
Standard Deviation
Score on a scale
Week 12
ID
Title
Description
OG000
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
OG001
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
Secondary
Change From Baseline in CDAI at Week 12 - RA
The Clinical Disease Activity Index (CDAI) is the sum of the tender joint score (range 0 to 28), the swollen joint score (range 0 to 28), the SGA of disease activity (range 0 to 10 in increments of 0.5), and the PGA of disease activity (range 0 to 10 in increments of 0.5). Baseline values are defined as the last nonmissing value prior to the first dose of study treatment. A CDAI score ranges from 0 to 76.
All treated participants with baseline and week 12 measurements (Prespecified for participants in the RA cohort only).
Posted
Mean
Standard Deviation
Score on a scale
Week 12
ID
Title
Description
OG000
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
OG001
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
Secondary
Percent of Participants With ACR20 Response Compared to Baseline at Week 12 - RA
ACR20 defined as both improvement of 20% in the number of tender and swollen joints and a 20% improvement in 3 of the following 5 criteria:
Subject global assessment (SGA)
Physician global assessment (PGA)
Functional ability measure
Pain visual analog scale (VAS)
Erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP).
Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
All Treated Participants (Prespecified for participants in the RA cohort only).
Posted
Number
95% Confidence Interval
Percent of Participants
Week 12
ID
Title
Description
OG000
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
OG001
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
Units
Secondary
Percent of Participants With ACR70 Response Compared to Baseline at Week 12 - RA
ACR70 is defined as both improvement of 70% in the number of tender and swollen joints and a 70% improvement in 3 of the following 5 criteria:
Subject global assessment (SGA)
Physician global assessment (PGA)
Functional ability measure
Pain visual analog scale (VAS)
Erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP).
Baseline values are defined as the last nonmissing value prior to the first dose of study treatment.
All Treated Participants (Prespecified for participants in the RA cohort only).
Posted
Number
95% Confidence Interval
Percent of Participants
Week 12
ID
Title
Description
OG000
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
OG001
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
Units
Time Frame
All-cause mortality was assessed from participants first dose to their study completion (up to approximately 32 weeks) SAEs and Other AEs were assessed from first dose to 30 days following last dose (up to approximately 30 weeks)
Description
TEAEs are defined as AEs that occur after the participant received first dose of study treatment or if a preexisting condition worsens in severity or becomes serious after receiving the first dose of study treatment up to 30 days after the last dose of study treatment.
All-Cause Mortality Comment
Not provided
Arm/Groups
ID
Title
Description
Deaths (Affected)
Deaths (At Risk)
Serious Events (Affected)
Serious Events (At Risk)
Other Events (Affected)
Other Events (At Risk)
EG000
SLE- Placebo
Participants with systemic lupus erythematosus (SLE) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
0
5
0
5
4
5
EG001
SLE- Branebrutinib
Participants with systemic lupus erythematosus (SLE) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
0
15
0
15
14
15
EG002
pSS- Placebo
Participants with primary Sjögren's syndrome (pSS) receive placebo once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
0
4
0
4
4
4
EG003
pSS- Branebrutinib
Participants with primary Sjögren's syndrome (pSS) receive branebrutinib 9mg once daily (QD) during a 24-week double-blind placebo-controlled treatment period.
0
10
0
10
8
10
EG004
RA- Placebo
Participants with rheumatoid arthritis (RA) receive placebo once daily (QD) during a 12-week double-blind placebo-controlled treatment period, followed by an additional 12 weeks of treatment with open-label abatacept.
0
21
0
21
6
21
EG005
RA- Branebrutinib
Participants with rheumatoid arthritis (RA) receive branebrutinib 9mg once daily (QD) during a 12-week double-blind placebo-controlled treatment period.
0
64
0
64
13
64
EG006
RA Abatacept
Participants with rheumatoid arthritis (RA) receive 12 weeks of treatment with open-label abatacept after the 12-week double-blind placebo-controlled treatment period.
0
81
0
81
5
81
Serious Adverse Events
Not provided
Other Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Thrombocytopenia
Blood and lymphatic system disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG0030 affected10 at risk
EG0040 affected21 at risk
EG0050 affected64 at risk
EG0060 affected81 at risk
Atrioventricular block first degree
Cardiac disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Ventricular extrasystoles
Cardiac disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Dry eye
Eye disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Ocular hyperaemia
Eye disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Diarrhoea
Gastrointestinal disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Enterocolitis
Gastrointestinal disorders
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Gastritis
Gastrointestinal disorders
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Nausea
Gastrointestinal disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0021 affected4 at risk
EG003
Asthenia
General disorders
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Discomfort
General disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0021 affected4 at risk
EG003
Injection site swelling
General disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Pyrexia
General disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0021 affected4 at risk
EG003
Bronchitis
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
COVID-19
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Gastroenteritis
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0012 affected15 at risk
EG0020 affected4 at risk
EG003
Hordeolum
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Nasopharyngitis
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0012 affected15 at risk
EG0023 affected4 at risk
EG003
Otitis media acute
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Pharyngotonsillitis
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Upper respiratory tract infection
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Urinary tract infection
Infections and infestations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0013 affected15 at risk
EG0020 affected4 at risk
EG003
Animal scratch
Injury, poisoning and procedural complications
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Face injury
Injury, poisoning and procedural complications
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Ligament sprain
Injury, poisoning and procedural complications
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Scratch
Injury, poisoning and procedural complications
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Sunburn
Injury, poisoning and procedural complications
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0021 affected4 at risk
EG003
Vaccination complication
Injury, poisoning and procedural complications
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Gamma-glutamyltransferase increased
Investigations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Gastric pH decreased
Investigations
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Neutrophil count decreased
Investigations
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Dyslipidaemia
Metabolism and nutrition disorders
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Hypertriglyceridaemia
Metabolism and nutrition disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Bursitis
Musculoskeletal and connective tissue disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0021 affected4 at risk
EG003
Myalgia
Musculoskeletal and connective tissue disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Rotator cuff syndrome
Musculoskeletal and connective tissue disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Basal cell carcinoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 25.1
Systematic Assessment
EG0001 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Headache
Nervous system disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0021 affected4 at risk
EG003
Somnolence
Nervous system disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Stress
Psychiatric disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0010 affected15 at risk
EG0020 affected4 at risk
EG003
Dyspnoea
Respiratory, thoracic and mediastinal disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Drug eruption
Skin and subcutaneous tissue disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Pruritus
Skin and subcutaneous tissue disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Urticaria
Skin and subcutaneous tissue disorders
MedDRA 25.1
Systematic Assessment
EG0000 affected5 at risk
EG0011 affected15 at risk
EG0020 affected4 at risk
EG003
Certain Agreements
Are all PI(s) employees of the sponsor?
No
Restriction Type
OTHER
Results Disclosure Restriction on PI(s)?
Yes
Other Details
Bristol-Myers Squibb Co. agreements with investigators vary; constant is our right to embargo communications regarding trial results prior to public release for a period ≤60 days from submittal for review. We will not prohibit investigators from publishing, but will prohibit the disclosure of previously undisclosed confidential information other than study results, and request postponement of single-center publications until after disclosure of the clinical trial's primary publication.