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Completed

NCT Number: NCT02915159

A Study to Assess the Efficacy and Safety of Abatacept in Adults With Active Primary Sjögrens Syndrome

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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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Organizacion Medica De Investigacion S.A. (Omi), Capital Federal, Buenos Aires, Argentina

Loading trial locations.

Who can participate

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

  • EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) score of at least 5
  • Positive anti-SS-A/Ro antibody at screening
  • meet the 2016 American College of Rheumatology (ACR) / European League Against Rheumatism Classification Criteria for Sjögren's Syndrome (EULAR SS)

Exclusion criteria

  • Secondary Sjögrens syndrome
  • Active life-threatening or organ-threatening complications of Sjögren's-syndrome
  • Other medical condition associated with sicca syndrome

Other protocol defined inclusion/exclusion criteria could apply

Treatment and study plan

Abatacept

Biological

Other names: Orencia, Bristol-Myers Squibb (BMS)-188667

Placebo

Other

Primary outcomes

  1. Change From Baseline in EULAR Sjogren's Syndrome Disease Activity Index (ESSDAI)

    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

Secondary outcomes

  1. Change From Baseline in EULAR Sjogren's Syndrome Patient Reported Inde (ESSPRI)

    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.

  2. Change From Baseline in the Stimulated Whole Salivary Flow

    Time frame: Day 169

    The mean change from baseline in the stimulated whole salivary flow at Day 169

  3. Change From Baseline of DAS28-C-reactive Peptide (CRP): In The Full Population

    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

  4. Change From Baseline of DAS28-CRP: Tender Swollen Joint Count of at Least 3

    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

  5. Change From Baseline of DAS28-CRP: Tender Swollen Joints Count Less Than 3

    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

  6. Change From Baseline in the Joint Component of DAS28-CRP: In the Full Population

    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

  7. Change From Baseline in the CRP Component of DAS28-CRP: In the Full Population

    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

  8. Change From Baseline in the Assessment of Disease Activity Component of DAS28-CRP: In the Full Population

    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

  9. Change From Baseline in the Joint Component of DAS28-CRP: Tender Swollen Joints of at Least 3

    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

  10. Change From Baseline in the CRP Component of DAS28-CRP: Tender Swollen Joints of at Least 3

    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

  11. Change From Baseline in the Assessment of Disease Activity Component of DAS28-CRP: Tender Swollen Joints of at Least 3

    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

  12. Change From Baseline in the Joint Component of DAS28-CRP: Tender Swollen Joint Count Less Than 3

    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

  13. Change From Baseline in the CRP Component of DAS28-CRP: Tender Swollen Joint Count Less Than 3

    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

  14. Change From Baseline in the Assessment of Disease Activity Component of DAS28-CRP: Tender Swollen Joint Count Less Than 3

    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

  15. Participants Who Achieve Minimally Clinically Important Change in ESSDAI in at Least 3 Points

    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.

  16. Participants Who Achieve Minimally Clinically Important Change in ESSDAI in at Least 5 Points

    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.

  17. Participants Who Achieve Minimally Clinically Important Change in ESSPRI in at Least 1 Point

    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.

  18. Change From Baseline at All Measured Time Points in the ESSDAI

    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

  19. Change From Baseline at All Measured Time Points in the ESSPRI

    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.

  20. Change From Baseline in Components of ESSDAI

    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)

  21. Change From Baseline in ESSPRI Components

    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.

  22. Change From Baseline in Schirmer's Test

    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.

  23. Change From Baseline in the Ocular Staining Score (OSS)

    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]

  24. Change From Baseline in Tear Break-up Time

    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.

  25. Change From Baseline in Unstimulated Salivary Flow

    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.

  26. Change From Baseline in Stimulated Salivary Flow

    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.

  27. Change From Baseline in Numeric Rating Scale for Mouth Dryness

    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

  28. Change From Baseline in Numeric Rating Scale for Eye 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

  29. Change From Baseline in Participant Assessment of Disease Activity

    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

  30. Change From Baseline in Physician Global Assessment of Disease Activity

    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

  31. Change From Baseline in Patient Fatigue

    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

  32. Change From Baseline in Female Sexual Function Using the Female Sexual Function Index (FSFI)

    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

  33. Change From Baseline in 36-item Short Form Health Survey (SF-36)

    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

  34. Geometric Mean of Trough Concentration (Cmin) of Abatacept

    Time frame: Day 29, 85, 113, 141, 169

    Geometric mean of trough concentration (Cmin) of abatacept at all measured time points.

  35. Percentage of Participants With a Positive Antibody Response

    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).

  36. Summary of Adverse Events: Double Blind Period

    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

  37. Laboratory Marked Abnormalities: Double Blind Period

    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

  38. Percentage of Participants With a Positive Antibody Response in the Cumulative Abatacept Period

    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.

  39. Summary of Adverse Events: Cumulative Abatacept 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

  40. Laboratory Marked Abnormalities: Cumulative Abatacept Period

    Time frame: Day 365 and 3 months of follow up approximately 450 Days

    Laboratory values meeting the marked abnormality criteria

Sponsors and collaborators

Lead sponsor

Bristol-Myers Squibb

Industry

Registry information

Official study title

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

Important dates

Study start
2016
Primary completion
2018
Study completion
2019
First posted
Sep 26, 2016
Registry last updated
Aug 10, 2020

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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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