Abatacept
BiologicalOther names: Orencia, Bristol-Myers Squibb (BMS)-188667
NCT Number: NCT02915159
The purpose of this study is to evaluate the efficacy of abatacept compared to placebo in patients with Sjögren's Syndrome.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Organizacion Medica De Investigacion S.A. (Omi), Capital Federal, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com
Inclusion criteria
Exclusion criteria
Other protocol defined inclusion/exclusion criteria could apply
Other names: Orencia, Bristol-Myers Squibb (BMS)-188667
Time frame: Day 169
The EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) total score is calculated as the sum of scores for activity level for each domain.
The EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) Scoring Algorithm.
Domain: (Score) Constitutional: (No=0, Low=3, Moderate=6) Lymphadenopathy: (No=0, Low=4, Moderate=8, High=12) Glandular: (No=0, Low=2, Moderate=4) Articular: (No=0, Low=2, Moderate=4, High=6) Cutaneous: (No=0, Low=3, Moderate=6, High=9) Pulmonary: (No=0, Low=5, Moderate=10, High=15) Renal: (No=0, Low=5, Moderate=10, High=15) Muscular: (No=0, Low=6, Moderate=12, High=18) Peripheral Nervous System (PNS): (No=0, Low=5, Moderate=10, High=15) Central Nervous System (CNS): (No=0, Moderate=10, High=15) Haematological: (No=0, Low=2, Moderate=4, High=6) Biological: (No=0, Low=1, Moderate=2)
(No = No Disease Activity (DA), Low = Low DA, Moderate = Moderate DA, High = High DA)
Overall score, which can range from 0 to 123, a higher score indicates more disease activity
Time frame: Day 169
The total score EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI) is calculated as the mean of the 3 individual components.
Total Score Range (0 = Best outcome and 10 = Worst Outcome)
The scores for the ESSPRI individual components will be used as such reported by the participants and entered in the case report form (CRF), without any further calculations. It consists of 3 questions covering cardinal symptoms of Sjögren's syndrome: dryness, fatigue and pain. Each domain scored on scale of 0-10 (0 =no symptom at all and 10 = worst symptom imaginable), and overall score is calculated as the mean of 3 individual domains.
Time frame: Day 169
The mean change from baseline in the stimulated whole salivary flow at Day 169
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The disease activity score DAS28-CRP is a continuous variable which is a composite of 4 variables: the 28 tender joint count (tender28), the 28 swollen joint count (swollen28), CRP and participant assessment of disease activity measure on a visual analogue scale (VAS) of 100mm.
DAS28-CRP = 0.56 * sqrt(tender28) + 0.28 * sqrt(swollen28) + 0.36 * ln(hsCRP+1) + 0.014 * VAS + 0.96.
(sqrt = Square root, ln = natural log)
Positive Scores = Increased Disease Activity Negative Scores = Reduced Disease Activity
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The disease activity score DAS28-CRP is a continuous variable which is a composite of 4 variables: the 28 tender joint count (tender28), the 28 swollen joint count (swollen28), CRP and participant assessment of disease activity measure on a visual analogue scale (VAS) of 100mm.
DAS28-CRP = 0.56 * sqrt(tender28) + 0.28 * sqrt(swollen28) + 0.36 * ln(hsCRP+1) + 0.014 * VAS + 0.96.
(sqrt = Square root, ln = natural log)
Positive Scores = Increased Disease Activity Negative Scores = Reduced Disease Activity
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The disease activity score DAS28-CRP is a continuous variable which is a composite of 4 variables: the 28 tender joint count (tender28), the 28 swollen joint count (swollen28), CRP and participant assessment of disease activity measure on a visual analogue scale (VAS) of 100mm.
DAS28-CRP = 0.56 * sqrt(tender28) + 0.28 * sqrt(swollen28) + 0.36 * ln(hsCRP+1) + 0.014 * VAS + 0.96.
(sqrt = Square root, ln = natural log)
Positive Scores = Increased Disease Activity Negative Scores = Reduced Disease Activity
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
Tender Joint: Count 1-28 Swollen Joint: Count 1-28
Negative Scores = Reduced number of joints impacted Positive Scores = Increased number of joints impacted
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
CRP: measured lab value
Positive Number = Increased level of CRP Negative Number = Reduced Level of CRP
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
Assesment of Disease Activity: 0-100 scale [100=Most severe]
Positive Numbers = Increased Disease Activity Negative Numbers = Decreased Diseased activity
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
Tender Joint: Count 1-28 Swollen Joint: Count 1-28
Negative Scores = Reduced number of joints impacted Positive Scores = Increased number of joints impacted
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
CRP: measured lab value
Positive Number = Increased level of CRP Negative Number = Reduced Level of CRP
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
Assesment of Disease Activity: 0-100 scale [100=Most severe]
Positive Numbers = Increased Disease Activity Negative Numbers = Decreased Diseased activity
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
Tender Joint: Count 1-28 Swollen Joint: Count 1-28
Negative Scores = Reduced number of joints impacted Positive Scores = Increased number of joints impacted
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
CRP: measured lab value
Positive Number = Increased level of CRP Negative Number = Reduced Level of CRP
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The mean change from baseline at all measured time points up to Day 169 in the individual components of DAS28-CRP.
Assesment of Disease Activity: 0-100 scale [100=Most severe]
Positive Numbers = Increased Disease Activity Negative Numbers = Decreased Diseased activity
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
Proportion of participants who achieve a minimally clinically important change (of at least 3 points) in the ESSDAI at all measured time points up to Day 169.
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
Proportion of participants who achieve a minimally clinically important change (of at least 5 points) in the ESSDAI at all measured time points up to Day 169.
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
Proportion of participants who achieve a minimally clinically important change (of at least 1 point) in the ESSPRI at all measured time points up to Day 169.
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) total score is calculated as the sum of scores for activity level for each domain.
The EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) Scoring Algorithm.
Domain: (Score) Constitutional: (No=0, Low=3, Moderate=6) Lymphadenopathy: (No=0, Low=4, Moderate=8, High=12) Glandular: (No=0, Low=2, Moderate=4) Articular: (No=0, Low=2, Moderate=4, High=6) Cutaneous: (No=0, Low=3, Moderate=6, High=9) Pulmonary: (No=0, Low=5, Moderate=10, High=15) Renal: (No=0, Low=5, Moderate=10, High=15) Muscular: (No=0, Low=6, Moderate=12, High=18) Peripheral Nervous System (PNS): (No=0, Low=5, Moderate=10, High=15) Central Nervous System (CNS): (No=0, Moderate=10, High=15) Haematological: (No=0, Low=2, Moderate=4, High=6) Biological: (No=0, Low=1, Moderate=2)
(No = No Disease Activity (DA), Low = Low DA, Moderate = Moderate DA, High = High DA)
Overall score, which can range from 0 to 123, a higher score indicates more disease activity
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The total score EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI) is calculated as the mean of the 3 individual components.
Total Score Range (0 = Best outcome and 10 = Worst Outcome)
The scores for the ESSPRI individual components will be used as such reported by the participants and entered in the case report form (CRF), without any further calculations. It consists of 3 questions covering cardinal symptoms of Sjögren's syndrome: dryness, fatigue and pain. Each domain scored on scale of 0-10 (0 =no symptom at all and 10 = worst symptom imaginable), and overall score is calculated as the mean of 3 individual domains.
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141 and Day 169
The EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) total score is calculated as the sum of scores for activity level for each domain.
The EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) Scoring Algorithm.
Domain: (Score for activity level) Constitutional: (No=0, Low=3, Moderate=6) Lymphadenopathy: (No=0, Low=4, Moderate=8, High=12) Glandular: (No=0, Low=2, Moderate=4) Articular: (No=0, Low=2, Moderate=4, High=6) Cutaneous: (No=0, Low=3, Moderate=6, High=9) Pulmonary: (No=0, Low=5, Moderate=10, High=15) Renal: (No=0, Low=5, Moderate=10, High=15) Muscular: (No=0, Low=6, Moderate=12, High=18) Peripheral Nervous System (PNS): (No=0, Low=5, Moderate=10, High=15) Central Nervous System (CNS): (No=0, Moderate=10, High=15) Haematological: (No=0, Low=2, Moderate=4, High=6) Biological: (No=0, Low=1, Moderate=2)
(No = No Disease Activity, Low = Low Disease Activity, Moderate = Moderate Disease Activity, High = High Disease Activity)
Time frame: Day 29, Day 57, Day 85, Day 113, Day 141, Day 169
The total score EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI) is calculated as the mean of the 3 individual components.
Total Score Range (0 = Best outcome and 10 = Worst Outcome)
The scores for the ESSPRI individual components will be used as such reported by the participants and entered in the case report form (CRF), without any further calculations. It consists of 3 questions covering cardinal symptoms of Sjögren's syndrome: dryness, fatigue and pain. Each domain scored on scale of 0-10 (0 =no symptom at all and 10 = worst symptom imaginable), and overall score is calculated as the mean of 3 individual domains.
Time frame: Day 85, Day 169
The Mean change from baseline in Schirmer's Test at all measured time points up to day 169
The length in millimeters that the strip wets during the 5 minute test period for each eye. Collection is done separately for each eye.
Time frame: Day 85, Day 169
The Mean change from baseline in OSS at all measured time points up to day 169
Score of 0 = No Staining Score of 12 = diffuse staining
The total score will be calculated as the sum of the score for these parameters for each eye.
Medial Nasal Bulbar Conjunctiva (MNBC) [score scale: 0 - 3], Corneal (CORN) Staining of Punctate Epithelial Erosions (PEE) [score scale: 0 - 3], Lateral Temporal Bulbar Conjunctiva (LTBC) [score scale: 0 - 3], Patches of Confluent Staining (CONF) [score scale: 0 - 1], PEE observed in the pupil region, i.e. central 4mm diameter portion of the cornea (PUPL) [score scale: 0 - 1], one of more filaments seen anywhere on the cornea (FILA) [score scale: 0 - 1]
Time frame: Day 85, Day 169
The Mean change from baseline in Tear Break-up Time at all measured time points up to day 169
The CRF collects the time in seconds to first appearance of a random dry spot on the corneal surface for 3 repetitions in each eye. The average time will calculated for each eye averaging the 3 measurements for each eye separately. In case only 2 measurements are available, the average of the 2 measurements will be calculated. In case there is only 1 measurement, that measurement will be used for the analysis.
Time frame: Day 85, Day 169
The mean change from baseline in unstimulated whole salivary flow at all measured time points up to Day 169.
Time frame: Day 85, Day 169
The mean change from baseline in Stimulated whole salivary flow at all measured time points up to Day 169.
Time frame: Day 1, 29, 57, 85, 113, 141, 169
The mean change from baseline in participant symptoms using the Numeric Rating Scale (NRS) for mouth dryness at all measured time points up to Day 169.
The oral and ocular dryness are each assessed by the patients with numeric rating scales from 0 to 10 with 0 representing no dryness and 10 representing maximal dryness
Time frame: Day 1, 29, 57, 85, 113, 141, 169
The mean change from baseline in patient symptoms using the Numeric Rating Scale (NRS) for eye dryness at all measured time points up to Day 169.
The oral and ocular dryness are each assessed by the patients with numeric rating scales from 0 to 10 with 0 representing no dryness and 10 representing maximal dryness
Time frame: Day 29, 57, 85, 113, 141, 169
The participant global assessment of disease activity are assessed with visual analog scales. The participant marks a vertical line through a horizontal line, where the beginning of the horizontal line represents the best situation, and the end of the horizontal line represents the very worst situation. The CRF collects the distance in millimeters from the start of the scale that is marked as well as the length of the scale in millimeters.
In cases that the length of the scale is in less or more than 100 millimeters, then the participants measurement will be rescaled to the equivalent of 100 millimeters using the formula below:
Rescale Measurement in mm = (measurement as reported on CRF in mm/length of the line on CRF in mm) * 100mm
A negative score = participant assessment of disease activity has improved
A positive score = participant assessment of disease activity has worsened
Time frame: Day 29, 57, 85, 113, 141, 169
The physician global assessment of disease activity are assessed with visual analog scales. The physician marks a vertical line through a horizontal line, where the beginning of the horizontal line represents the best situation, and the end of the horizontal line represents the very worst situation. The CRF collects the distance in millimeters from the start of the scale that is marked as well as the length of the scale in millimeters.
In cases that the length of the scale is in less or more than 100 millimeters, then the participants measurement will be rescaled to the equivalent of 100 millimeters using the formula below:
Rescale Measurement in mm = (measurement as reported on CRF in mm/length of the line on CRF in mm) * 100mm
A negative score = physician assessment of disease activity has improved
A positive score = physician assessment of disease activity has worsened
Time frame: Day 29, 57, 85, 113, 141, 169
The mean change from baseline in patient fatigue using Patient Reported Outcomes Measurement Information System (PROMIS) Fatigue assessment of disease activity at all measured time points up to Day 169.
PROMIS Fatigue instruments 10 Questions ranging from a score 0 to 40. Sum of the values gives you the raw sum. The raw is inputted into this formula to give you the raw score:
Raw Score = (Raw sum*number of items on the short form)/(Number of items that were actually answered)
Raw score is translated to a T-Score using a table. T-Score is used as the final score.
The T-score rescales the raw score into a standardized score with a mean of 50 and a standard deviation (SD) of 10. The standardized T-score is reported as the final score for each participant.
A negative T Score = Better Prognosis A positive T Score = Worse prognosis
Time frame: Day 85, Day 169
For the FSFI, is a 19 item instrument used for assessing key dimensions of female sexual function over the past 4 weeks with 6 domains being analyzed. The specific domains (desire, arousal, lubrication, orgasm, satisfaction, and pain) analyzed in the FSFI are scored on a scale ranging from 0 to 5, with higher scores indicating better performance. Domain scores are calculated by summing the scores of the individual questions that make up the domain and multiplying the sum by the factor in the table below. The full scale score is the sum of the six domain scores.
Full Scale Score range: 2.0(minimum score) - 36.0 (maximum score)
Negative Score = Reduced functioning Positive Score = Improved functioning
Time frame: Day 85, Day 169
The SF-36 determines participants' overall quality of life by assessing 1) limitations in physical functioning due to health problems; 2) limitations in usual role because of physical health problems; 3) bodily pain; 4) general health perceptions; 5) vitality; 6) limitations in social functioning because of physical or emotional problems; 7) limitations in usual role due to emotional problems; and 8) general mental health.
Scores on each item are summed and averaged (range: 0=worst to 100=best). Increases from baseline indicate improvement
Time frame: Day 29, 85, 113, 141, 169
Geometric mean of trough concentration (Cmin) of abatacept at all measured time points.
Time frame: Day 85 db, day 169 db, post treatment day 85
Percentage of participants with at least one positive immunogenicity response up to Day 169 and during 3 months follow up (for participants who discontinue during the 6-months double-blind).
Time frame: Day 1 up to first dose of Open Label Treatment Period (OLTP) abatacept or up to 56 post last dose in double -blind for those not in OL.
Percentage of participants with adverse events, deaths, serious adverse events and adverse events leading to discontinuation
Time frame: Day 1 up to first dose of OL abatacept or up to 56 post last dose in double -blind for those not in OL.
Laboratory values meeting the marked abnormality criteria
Time frame: Day 365, post open label treatment day 85
Percentage of participants with at least one positive immunogenicity response On Day 365 (end of Open label treatment period) and day 85 post open label follow up period.
Time frame: Day 365 and 3 months of follow up approximately 450 Days
Percentage of participants with adverse events, deaths, serious adverse events and adverse events leading to discontinuation
Time frame: Day 365 and 3 months of follow up approximately 450 Days
Laboratory values meeting the marked abnormality criteria
Bristol-Myers Squibb
Industry
A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Subcutaneous Abatacept in Adults With Active Primary Sjögrens Syndrome
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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