A Study to Determine the Efficacy and Safety of Deucravacitinib Compared With Placebo in Participants With Active Psoriatic Arthritis (PsA) Who Are Naïve to Biologic Disease-modifying Anti-rheumatic Drugs

Recruitment Status
ACTIVE, NOT RECRUITING - HAS RESULTS
(See Contacts and Locations)Verified March 2026 by Bristol-Myers Squibb
Sponsor
Bristol-Myers Squibb
Information Provided by (Responsible Party)
Bristol-Myers Squibb
Clinicaltrials.gov Identifier
NCT04908202
Other Study ID Numbers:
IM011-054
First Submitted
May 27, 2021
First Posted
May 31, 2021
Results First Posted
September 1, 2025
Last Update Posted
April 22, 2026
Last Verified
March 2026

ClinicalTrials.gov processed this data on April 2026Link to the current ClinicalTrials.gov record .

History of Changes

Study Details

Study Description

Condition or DiseaseIntervention/Treatment
Psoriatic Arthritis
Drug: DeucravacitinibOther: Placebo

Study Design

Study TypeInterventional
Actual Enrollment670 participants
Design AllocationRandomized
Interventional ModelParallel Assignment
MaskingQuadruple
Primary PurposeTreatment
Official TitleA Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Deucravacitinib in Participants With Active Psoriatic Arthritis Who Are Naïve to Biologic Disease-modifying Anti-rheumatic Drugs
Study Start DateJuly 12, 2021
Actual Primary Completion DateSeptember 4, 2024
Actual Study Completion Date1yr 3w from now

Groups and Cohorts

Group/CohortIntervention/Treatment
Deucravacitinib
Drug: Deucravacitinib
Specified dose on specified days
Placebo
Other: Placebo
Specified dose on specified days

Outcome Measures

Primary Outcome Measures
  1. Percentage of Participants With ACR 20 Response at Week 16
    The ACR 20 definition of improvement is a 20% improvement over baseline in tender and swollen joint counts (#1 and #2) and a 20% improvement in 3 of the 5 remaining core data set measures (Participant global assessment of pain, participant global assessment of disease activity, physician global assessment of disease activity, participant assessment of physical function, and acute phase reactant value). Baseline value is the last assessment taken prior to first dose of single-blind study medication. The 95% CI is calculated using Clopper-Pearson exact method.
Secondary Outcome Measures
  1. Change From Baseline in Disease Activity Score 28 C-reactive Protein (DAS28-CRP) at Week 16
    DAS28-CRP is a composite of how many joints in the hands (including metacarpophalangeal and proximal interphalangeal joints but excluding DIPs), wrists, elbows, shoulders, and knees are swollen and/or tender out of a total of 28; CRP in the blood to measure the degree of inflammation, and participant global assessment of disease activity. The results are combined to produce the DAS28-CRP score that range from 1.0 to 9.4, which correlates with the extent of disease activity: \< 2.6=disease remission; 2.6 - 3.2=low disease activity; 3.2-5.1=moderate disease activity; \>5.1=high disease activity. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in DAS28-CRP indicates an improvement.
  2. Change From Baseline in Health Assessment Questionnaire - Disability Index (HAQ-DI) at Week 16
    HAQ-DI is a patient-reported outcome measure that assesses the degree of difficulty a participant has experienced during the past week in 8 domains of daily living activities: dressing and grooming, arising, eating, walking, hygiene, reach, grip, and other activities. Each activity category consists of 2 to 3 items. For each item in the questionnaire, the level of activity is scored from 0 to 3, with 0 representing "no difficulty," 1 representing "some difficulty," 2 representing "much difficulty," and 3 representing "unable to do." increasing scores for the 8 disability categories indicate increasing level of difficulty. HAQDI is calculated by summing the adjusted categories scores and dividing by the number of categories answered. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in HAQ-DI indicates an improvement.
  3. Percentage of Participants Meeting Psoriatic Area and Severity Index (PASI) 75 Response at Week 16, in Participants With at Least 3% Body Surface Area (BSA) Involvement and at Least Static Physician's Global Assessment (sPGA) 2 at Baseline
    PASI is a measure of the average erythema, induration thickness, and scaling of psoriatic skin lesions (each graded on a 0 to 4 scale), weighted by the area of involvement (head, arms, trunk to groin, and legs to top of buttocks). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. PASI 75 is the number of participants who experience at least a 75% improvement in PASI score as compared with the baseline value. The 95% CI is calculated using Clopper-Pearson exact method.
  4. Change From Baseline in the 36-item Short Form (SF-36) Physical Subcomponent Summary (PCS) Score at Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The physical subcomponent summary (PCS) consists of these 4 subscales: Physical functioning, Role-physical, Bodily pain, General health. The scores range from 0 to 100, with a higher score indicating better quality of life. The PCS summary scores will be calculated by taking a weighted linear combination of the individual subscales. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 PCS indicates an improvement.
  5. Percentage of Participants Meeting Enthesitis Resolution (Score of 0) Among Participants With Enthesitis at Baseline by Leeds Enthesitis Index (LEI) at Week 16
    Percentage of participants meeting enthesitis resolution (score of 0) among participants with enthesitis at Baseline by Leeds Enthesitis Index (LEI). An overall score of 0 to 6 is derived from the presence or absence of tenderness at 6 enthesial sites (right and left: lateral epicondyle, medial femoral condyle, and Achilles tendon insertion) at the time of evaluation. A higher count indicates a greater enthesitis burden.
  6. Percentage of Participants Meeting Achievement of Minimal Disease Activity (MDA) at Week 16
    Percentage of participants meeting achievement of MDA where an MDA response is achievement of 5 of 7 following outcomes at Week 16: 1. Tender joint count \<= 1 2. Swollen joint count \<=1 3. Psoriasis Area and Severity Index (PASI) \<= 1 or body surface area (BSA) \<= 3% 4. Patient assessment of psoriatic arthiritis (PsA) pain \<= 15 5. Patient Global Assessment of PsA disease activity \<= 20 6. HAQ-DI \<= 0.5 7. Tender enthesial points \<= 1
  7. Change From Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-Fatigue) Score at Week 16
    FACIT-Fatigue evaluates a range of self-reported symptoms over the past week, from mild subjective feelings of tiredness to an overwhelming, debilitating, and sustained sense of exhaustion that likely decreases one's ability to execute daily activities and function normally in family or social roles. Fatigue is divided into the experience or symptoms of fatigue (frequency, duration, and intensity) and the impact of fatigue on physical, mental, and social activities. The recall period is 7 days. Each item is rated on a 5-point Likert scale ranging from 0 = "not at all" to 4 = "very much." Sum scores for the 13 items range from 0 through 52, where higher scores indicate less fatigue. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in FACIT-Fatigue indicates an improvement.
  8. Percentage of Participants Meeting Dactylitis Resolution at Week 16
    Percentage of participants meeting dactylitis resolution at Week 16 among the participants with dactylitis at baseline, where resolution is defined as a tender dactylitis count of 0 in participants with a tender dactylitis count =\> 1 at baseline. The number of digits in hands and feet with dactylitis will be counted by a blinded assessor.
  9. Change From Baseline in PsA-modified Sharp-van Der Heijde (SvdH) Score at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage. Change from baseline reflects progression or improvement; a decrease suggests reduced damage or improvement.
  10. Percentage of Participants With ACR 20 Response up to Week 16
    The ACR 20 definition of improvement is a 20% improvement over baseline in tender and swollen joint counts (#1 and #2) and a 20% improvement in 3 of the 5 remaining core data set measures (Participant global assessment of pain, participant global assessment of disease activity, physician global assessment of disease activity, participant assessment of physical function, and acute phase reactant value). Baseline value is the last assessment taken prior to first dose of single-blind study medication. The 95% CI is calculated using Clopper-Pearson exact method.
  11. Percentage of Participants With ACR 50 Response up to Week 16
    The ACR 50 definition of improvement is a 50% improvement over baseline in tender and swollen joint counts (#1 and #2) and a 50% improvement in 3 of the 5 remaining core data set measures (Participant global assessment of pain, participant global assessment of disease activity, physician global assessment of disease activity, participant assessment of physical function, and acute phase reactant value). Baseline value is the last assessment taken prior to first dose of single-blind study medication. The 95% CI is calculated using Clopper-Pearson exact method.
  12. Percentage of Participants With ACR 70 Response up to Week 16
    The ACR 70 definition of improvement is a 70% improvement over baseline in tender and swollen joint counts (#1 and #2) and a 70% improvement in 3 of the 5 remaining core data set measures (Participant global assessment of pain, participant global assessment of disease activity, physician global assessment of disease activity, participant assessment of physical function, and acute phase reactant value). Baseline value is the last assessment taken prior to first dose of single-blind study medication. The 95% CI is calculated using Clopper-Pearson exact method.
  13. Change From Baseline in Health Assessment Questionnaire - Disability Index (HAQ-DI) up to Week 16
    HAQ-DI is a patient-reported outcome measure that assesses the degree of difficulty a participant has experienced during the past week in 8 domains of daily living activities: dressing and grooming, arising, eating, walking, hygiene, reach, grip, and other activities. Each activity category consists of 2 to 3 items. For each item in the questionnaire, the level of activity is scored from 0 to 3, with 0 representing "no difficulty," 1 representing "some difficulty," 2 representing "much difficulty," and 3 representing "unable to do." increasing scores for the 8 disability categories indicate increasing level of difficulty. HAQDI is calculated by summing the adjusted categories scores and dividing by the number of categories answered. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in HAQ-DI indicates an improvement.
  14. Percentage of Participants Who Achieve a Clinically Meaningful Improvement in Health Assessment Questionnaire - Disability Index (HAQ-DI) up to Week 16 Among Participants With a HAQ-DI Score ≥0.35 at Baseline
    HAQ-DI is a patient-reported outcome measure that assesses the degree of difficulty a participant has experienced during the past week in 8 domains of daily living activities: dressing and grooming, arising, eating, walking, hygiene, reach, grip, and other activities. Each activity category consists of 2 to 3 items. For each item in the questionnaire, the level of activity is scored from 0 to 3, with 0 representing "no difficulty," 1 representing "some difficulty," 2 representing "much difficulty," and 3 representing "unable to do." increasing scores for the 8 disability categories indicate increasing level of difficulty. HAQDI is calculated by summing the adjusted categories scores and dividing by the number of categories answered. Clinically meaningful improvement was defined as ≥0.35improvement from baseline.
  15. Percentage of Participants Meeting Psoriatic Area and Severity Index (PASI) 75 Response up to Week 16, in Participants With at Least 3% Body Surface Area (BSA) Involvement and at Least Static Physician's Global Assessment (sPGA) 2 at Baseline
    PASI is a measure of the average erythema, induration thickness, and scaling of psoriatic skin lesions (each graded on a 0 to 4 scale), weighted by the area of involvement (head, arms, trunk to groin, and legs to top of buttocks). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. PASI 75 is the number of participants who experience at least a 75% improvement in PASI score as compared with the baseline value. The 95% CI is calculated using Clopper-Pearson exact method.
  16. Percentage of Participants Meeting Psoriatic Area and Severity Index (PASI) 90 Response up to Week 16, in Participants With at Least 3% Body Surface Area (BSA) Involvement and at Least Static Physician's Global Assessment (sPGA) 2 at Baseline
    PASI is a measure of the average erythema, induration thickness, and scaling of psoriatic skin lesions (each graded on a 0 to 4 scale), weighted by the area of involvement (head, arms, trunk to groin, and legs to top of buttocks). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. PASI 90 is the number of participants who experience at least a 90% improvement in PASI score as compared with the baseline value. The 95% CI is calculated using Clopper-Pearson exact method.
  17. Percentage of Participants Meeting Psoriatic Area and Severity Index (PASI) 100 Response up to Week 16, in Participants With at Least 3% Body Surface Area (BSA) Involvement and at Least Static Physician's Global Assessment (sPGA) 2 at Baseline
    PASI is a measure of the average erythema, induration thickness, and scaling of psoriatic skin lesions (each graded on a 0 to 4 scale), weighted by the area of involvement (head, arms, trunk to groin, and legs to top of buttocks). The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity. PASI 100 is the number of participants who experience at least a 100% improvement in PASI score as compared with the baseline value. The 95% CI is calculated using Clopper-Pearson exact method.
  18. Change From Baseline in the 36-item Short Form (SF-36) Physical Subcomponent Summary (PCS) Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The physical subcomponent summary (PCS) consists of these 4 subscales: Physical functioning, Role-physical, Bodily pain, General health. The scores range from 0 to 100, with a higher score indicating poor quality of life. The PCS summary scores will be calculated by taking a weighted linear combination of the individual subscales. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 PCS indicates an improvement.
  19. Percentage of Participants Meeting Enthesitis Resolution (Score of 0) Among Participants With Enthesitis at Baseline by Leeds Enthesitis Index (LEI) up to Week 16
    Percentage of participants meeting enthesitis resolution (score of 0) among participants with enthesitis at Baseline by Leeds Enthesitis Index (LEI). An overall score of 0 to 6 is derived from the presence or absence of tenderness at 6 enthesial sites (right and left: lateral epicondyle, medial femoral condyle, and Achilles tendon insertion) at the time of evaluation. A higher count indicates a greater enthesitis burden.
  20. Percentage of Participants Meeting Enthesitis Resolution (Score of 0) Among Participants With Enthesitis at Baseline by Spondyloarthritis Research Consortium of Canada (SPARCC) up to Week 16
    Percentage of participants meeting enthesitis resolution (score of 0) among participants with enthesitis at Baseline by SPARCC. The SPARCC Enthesitis Index has a 0 to 16 score that is derived from the evaluation of 8 locations: the greater trochanter (right \\\[R\\\]/left \\\[L\\\]), quadriceps tendon insertion into the patella (R/L), patellar ligament insertion into the patella and tibial tuberosity (R/L), Achilles tendon insertion (R/L), plantar fascia insertion (R/L), medial and lateral epicondyles (R/L), and supraspinatus insertion (R/L). A higher count indicates a higher enthesitis burden based on the current evaluation.
  21. Percentage of Participants Meeting Achievement of Minimal Disease Activity (MDA) up to Week 16
    Percentage of participants meeting achievement of MDA where an MDA response is achievement of 5 of 7 following outcomes at Week 16: 1. Tender joint count \<= 1 2. Swollen joint count \<=1 3. Psoriasis Area and Severity Index (PASI) \<= 1 or body surface area (BSA) \<= 3% 4. Patient assessment of psoriatic arthiritis (PsA) pain \<= 15 5. Patient Global Assessment of PsA disease activity \<= 20 6. HAQ-DI \<= 0.5 7. Tender enthesial points \<= 1
  22. Change From Baseline in the 36-item Short Form (SF-36) Mental Component Summary (MCS) Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The mental component summary (MCS) of the SF-36 consists of these 4 subscales: Vitality, Social functioning, Role-emotional, Mental health. The scores range from 0 to 100, with a higher score indicating poor quality of life. The MCS summary scores will be calculated by taking a weighted linear combination of the individual subscales. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 MCS indicates an improvement.
  23. Change From Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-Fatigue) Score up to Week 16
    FACIT-Fatigue evaluates a range of self-reported symptoms over the past week, from mild subjective feelings of tiredness to an overwhelming, debilitating, and sustained sense of exhaustion that likely decreases one's ability to execute daily activities and function normally in family or social roles. Fatigue is divided into the experience or symptoms of fatigue (frequency, duration, and intensity) and the impact of fatigue on physical, mental, and social activities. The recall period is 7 days. Each item is rated on a 5-point Likert scale ranging from 0 = "not at all" to 4 = "very much." Sum scores for the 13 items range from 0 through 52, where higher scores indicate less fatigue. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in FACIT-Fatigue indicates an improvement.
  24. Percentage of Participants Meeting Dactylitis Resolution up to Week 16
    Percentage of participants meeting dactylitis resolution at Week 16 among the participants with dactylitis at baseline, where resolution is defined as a tender dactylitis count of 0 in participants with a tender dactylitis count =\> 1 at baseline. The number of digits in hands and feet with dactylitis will be counted by a blinded assessor.
  25. Change From Baseline in Psoriatic Arthritis Impact of Disease (PsAID) 12 Score up to Week 16
    The Psoriatic Arthritis Impact of Disease (PsAID) is a 12-item self-report that measures PsA symptoms and impact of disease. Each item is scored on a 0 to 10 numeric rating scale with a 1-week recall period. The PsAID has a total score, with a higher value indicating worse health. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in PsAID indicates an improvement.
  26. Change From Baseline in Disease Activity Index for Psoriatic Arthritis (DAPSA) Score up to Week 16
    The Disease Activity Index for Psoriatic Arthritis Score is a composite measure to assess peripheral joint involvement that is based upon numerical summation of 5 variables of disease activity: tender joint count (0-68), swollen joint count (0-66), Participant Global Assessment of Disease Activity (0 to 10 cm VAS, 0= excellent and 10= poor), Participant Global Assessment of Pain (0 to 10 centimeter \\\[cm\\\] visual analog scale (VAS), 0= no pain, 10= worst possible pain), and C-reactive protein. The DAPSA score ranges from 0 to 154, with a higher score indicating more disease activity. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in DAPSA indicates an improvement.
  27. Percentage of Participants With Achievement of Disease Activity Index for Psoriatic Arthritis (DAPSA) Low Disease Activity Response up to Week 16
    The Disease Activity Index for Psoriatic Arthritis Score is a composite measure to assess peripheral joint involvement that is based upon numerical summation of 5 variables of disease activity: tender joint count (0-68), swollen joint count (0-66), Participant Global Assessment of Disease Activity (0 to 10 cm VAS, 0= excellent and 10= poor), Participant Global Assessment of Pain (0 to 10 centimeter \\\[cm\\\] visual analog scale (VAS), 0= no pain, 10= worst possible pain), and C-reactive protein. A higher DAPSA score indicated more active disease activity.
  28. Percentage of Participants With Achievement of Disease Activity Index for Psoriatic Arthritis (DAPSA) Disease Remission up to Week 16
    The Disease Activity Index for Psoriatic Arthritis Score is a composite measure to assess peripheral joint involvement that is based upon numerical summation of 5 variables of disease activity: tender joint count (0-68), swollen joint count (0-66), Participant Global Assessment of Disease Activity (0 to 10 cm VAS, 0= excellent and 10= poor), Participant Global Assessment of Pain (0 to 10 centimeter \\\[cm\\\] visual analog scale (VAS), 0= no pain, 10= worst possible pain), and C-reactive protein. A higher DAPSA score indicated more active disease activity. A score 0 signifies remission.
  29. Percentage of Participants Meeting Achievement of Physician Global Assessment-Fingernails (PGA-F) of 0/1 up to Week 16
    The PGA-F is a 5-point scale used to assess fingernails separately for nail bed signs and nail matrix signs of disease. A global score of between 0 indicating clear, and 4 indicating severe. The overall condition of the fingernails is rated on a 5-point scale: 0 = clear, 1 = minimal, 2 = mild, 3 = moderate, and 4 = severe.
  30. Change From Baseline in Disease Activity Score 28 C-reactive Protein (DAS28-CRP) up to Week 16
    DAS28-CRP is a composite of how many joints in the hands (including metacarpophalangeal and proximal interphalangeal joints but excluding DIPs), wrists, elbows, shoulders, and knees are swollen and/or tender out of a total of 28; CRP in the blood to measure the degree of inflammation, and participant global assessment of disease activity. The results are combined to produce the DAS28-CRP score that range from 1.0 to 9.4, which correlates with the extent of disease activity: \\\< 2.6=disease remission; 2.6 - 3.2=low disease activity; 3.2-5.1=moderate disease activity; \\\>5.1=high disease activity. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in DAS28-CRP indicates an improvement.
  31. Percentage of Participants Meeting Disease Activity Score 28 C-reactive Protein (DAS28-CRP) Low Disease Activity Response up to Week 16
    DAS28-CRP is a composite of how many joints in the hands (including metacarpophalangeal and proximal interphalangeal joints but excluding DIPs), wrists, elbows, shoulders, and knees are swollen and/or tender out of a total of 28; CRP in the blood to measure the degree of inflammation, and participant global assessment of disease activity. The results are combined to produce the DAS28-CRP score that range from 1.0 to 9.4, which correlates with the extent of disease activity: \\\< 2.6=disease remission; 2.6 - 3.2=low disease activity; 3.2-5.1=moderate disease activity; \\\>5.1=high disease activity.
  32. Percentage of Participants Meeting Disease Activity Score 28 C-reactive Protein (DAS28-CRP) Disease Remission up to Week 16
    DAS28-CRP is a composite of how many joints in the hands (including metacarpophalangeal and proximal interphalangeal joints but excluding DIPs), wrists, elbows, shoulders, and knees are swollen and/or tender out of a total of 28; CRP in the blood to measure the degree of inflammation, and participant global assessment of disease activity. The results are combined to produce the DAS28-CRP score that range from 1.0 to 9.4, which correlates with the extent of disease activity: \\\< 2.6=disease remission; 2.6 - 3.2=low disease activity; 3.2-5.1=moderate disease activity; \\\>5.1=high disease activity.
  33. Change From Baseline in Psoriatic Arthritis Disease Activity Score (PASDAS) up to Week 16
    The Psoriatic Arthritis Disease Activity Score (PASDAS) is a composite measure calculated from the Physician Global Assessment of PsA, the Participant Global Assessment of Disease Activity, the Short Form-36 PCS, the swollen joint count, the tender joint count, the Enthesitis (LEI), the Dactylitis (LDI) (Basic), and the High-sensitivity C-reactive protein (hsCRP). The range of PASDAS is 0-10. Higher score means more active disease. Change from baseline is defined as value at post-baseline visit. A negative change from baseline indicates an improvement.
  34. Change From Baseline in Modified Composite Psoriatic Disease Activity Index (mCPDAI) up to Week 16
    Four domains are used to calculate the modified Composite Psoriatic Disease Activity Index (mCPDAI): joints (66 swollen joint count and 68 tender joint count; Health Assessment Questionnaire), skin (PASI and DLQI), dactylitis (a simple count of each digit involved), and enthesitis (number of tendons/fascia insertion sites showing enthesitis scored from 0 to 4, based on palpation of Achilles tendon and bilateral plantar fasciae insertion). The mCPDAI is scored using a 4 point scale from 0 (no disease activity) to 3 (most severe disease activity), giving an mCPDAI score range of 0 through 12. A higher score indicates more active disease activity. Change from baseline is defined as value at post-baseline visit. A negative change from baseline indicates an improvement.
  35. Percentage of Participants With Achievement of Psoriatic Arthritis Response Criteria (PsARC) up to Week 16
    The Psoriatic Arthritis Response Criteria (PsARC) consists of 4 measurements: tender joint count, swollen joint count, Physician Global Assessment of PsA, and Participant Global Assessment of Disease Activity. In order to be classified as a PsARC responder, participants must achieve improvement in 2 of 4 measures, 1 of which must be joint pain or swelling, without worsening in any measure. Improvement in each of the measures is defined below: 1) Decrease of ≥ 30% in tender joint counts; 2) Decrease of ≥ 30% in swollen joint counts; 3) Decrease of ≥ 20% in Physician Global Assessment of PsA; 4) Decrease of ≥ 20% in Participant's Global Assessment of Disease Activity
  36. Percentage of Participants Meeting Achievement of Improvement of Bath Ankylosing Spondylitis Disease Activity (BASDAI) Score up to Week 16
    BASDAI consists of a 0 to 10 scale measuring discomfort, pain, and fatigue in response to 6 questions pertaining to the 5 major symptoms of ankylosing spondylitis: 1) Fatigue (medical); 2) Spinal pain; 3) Joint pain and swelling; 4) Areas of localized tenderness; 5) Morning stiffness duration; 6) Morning stiffness severity. A higher count indicates worse disease. Each individual question response is scaled to a 0-10 score by dividing by 10, and the BASDAI is derived using the following formula: BASDAI = ((Q1 + Q2 + Q3 + Q4) + ((Q5 + Q6) / 2)) / 5
  37. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Scores Response of <= 0 at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  38. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Scores Response of <= 0.5 at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  39. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Scores Response of <= Smallest Detectable Change (SDC) at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage. SDC is calculated as 1.96\* standard deviation of the paired differences of change from baseline/ square root of (2\*k); k is the number of reviewers and is default to 2 in this study.
  40. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Erosion Scores Response of <= 0 at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  41. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Erosion Scores Response of <= 0.5 at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  42. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Erosion Scores Response of <= SDC at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage. SDC is calculated as 1.96\* standard deviation of the paired differences of change from baseline/ square root of (2\*k); k is the number of reviewers and is default to 2 in this study.
  43. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Joint Space Narrowing (JSN) Scores Response of <= 0 at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  44. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Joint Space Narrowing (JSN) Scores Response of <= 0.5 at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  45. Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Joint Space Narrowing (JSN) Scores Response of <= SDC at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage. SDC is calculated as 1.96\* standard deviation of the paired differences of change from baseline/ square root of (2\*k); k is the number of reviewers and is default to 2 in this study.
  46. Change From Baseline in PsA-modified SvdH Erosion Scores Response at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  47. Change From Baseline in PsA-modified SvdH JSN Scores Response at Week 16
    The PsA-modified Sharp-van der Heijde (SvdH) score is a radiographic tool used to assess structural joint damage in psoriatic arthritis. It evaluates erosions, joint space narrowing, (sub)luxation, and ankylosis in 52 joints of the hands and feet, including distal interphalangeal joints. Erosions are scored 0-3 and joint space narrowing 0-4. The total score ranges from 0 to 528 (erosions: max 320; joint space narrowing: max 208). Higher scores indicate greater joint damage.
  48. Change From Baseline in the 36-item Short Form (SF-36) Physical Subcomponent Summary Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The physical sub component is one of the 4 subscales of PCS. The physical subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 physical sub-component indicates an improvement.
  49. Change From Baseline in the 36-item Short Form (SF-36) Role Activity Subcomponent Summary Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The role activity sub component is one of the 4 subscales of PCS. The role activity subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 role activity indicates an improvement.
  50. Change From Baseline in the 36-item Short Form (SF-36) Bodily Pain Subcomponent Summary Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The bodily pain sub component is one of the 4 subscales of PCS. The bodily pain subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 bodily pain subcomponent indicates an improvement.
  51. Change From Baseline in the 36-item Short Form (SF-36) General Health Perceptions Subcomponent Summary Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The general health perceptions sub component is one of the 4 subscales of PCS. The general health perceptions subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 general health perceptions subcomponent indicates an improvement.
  52. Change From Baseline in the 36-item Short Form (SF-36) Vitality Subcomponent Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The vitality subcomponent is one of the 4 subscales of MCS. The vitality subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 vitality subcomponent indicates an improvement.
  53. Change From Baseline in the 36-item Short Form (SF-36) Social Subcomponent Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The social subcomponent is one of the 4 subscales of MCS. The social subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 social subcomponent indicates an improvement.
  54. Change From Baseline in the 36-item Short Form (SF-36) Mental Health Subcomponent Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The mental health subcomponent is one of the 4 subscales of MCS. The mental health subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 mental health subcomponent indicates an improvement.
  55. Change From Baseline in the 36-item Short Form (SF-36) Emotional Problems Subcomponent Score up to Week 16
    SF-36 is a generic 36-item questionnaire measuring health-related quality of life. The emotional problem subcomponent is one of the 4 subscales of MCS. The emotional problem subcomponent scores will be calculated by taking a weighted linear combination of the individual question. The score ranges from 0 to 100, with higher values indication poor quality of life. Change from baseline is defined as value at post-baseline visit. A negative change from baseline in SF-36 emotional problems subcomponent indicates an improvement.
  56. Change From Baseline in the Work Productivity and Activity Impairment (WPAI) Subcomponents Score at Week 16
    WPAI contains 4 subcomponents - absenteeism (work time missed), presenteeism (impairment at work/reduced on-the-job effectiveness), work productivity (overall work impairment/absenteeism plus presenteeism), and activity impairment. Each subcomponent score ranges from 0 to 100, with higher numbers indicating worse outcome. Change from baseline is defined as value at post-baseline visit. A negative change from baseline indicates an improvement.
  57. Change From Baseline in the European Quality of Life 5D-5L (EQ-5D-5L) Utility Scores and Its Subcomponents up to 16
    The European Quality of Life 5D-5L Scale (EQ-5D-5L) assesses general health-related quality of life. Health is defined in 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems, and extreme problems. Responses are coded so that a &#039;1&#039; indicates no problem, and &#039;5&#039; indicates the most serious problem. The responses for the 5 dimensions are combined in a 5-digit number. Change from Baseline in 5-level EuroQol 5-dimension (EQ-5D-5L) Utility Scores. Change from baseline is defined as value at post-baseline visit. A negative change from baseline indicates an improvement.
  58. Change From Baseline in Patient-Reported Outcome Measures Information System (PROMIS) Sleep Disturbance up to Week 16
    The Patient-Reported Outcome Measures Information System Sleep Disturbance assess self-reported perceptions of sleep quality, sleep depth, and restoration associated with sleep. This includes perceived difficulties and concerns with getting to sleep or staying asleep, as well as perceptions of the adequacy of and satisfaction with sleep. The items are evaluated on a 5-point Likert scale ranging from 1 = &quot;not at all&quot; to 5 = &quot;very much&quot; with a 7-day recall period. Higher score means more active disease. Change from baseline is defined as value at post-baseline visit. A negative change from baseline indicates an improvement.

Eligibility Criteria

Ages Eligible for Study(Adult, Older Adult)
Sexes Eligible for StudyAll
Accepts Healthy VolunteersNo
Inclusion Criteria
Inclusion Criteria
Diagnosed to have psoriatic arthritis (PsA) of at least 3 months duration at screening.
Meets the Classification Criteria for Psoriatic Arthritis at Screening.
Active plaque psoriatic skin lesion(s) or documented medical history of plaque psoriasis (PsO) at screening.
Active arthritis as shown by ≥ 3 swollen joints and ≥ 3 tender joints at Screening and day 1.
Participant has high sensitivity C-reactive protein (hsCRP) ≥ 3 mg/L at Screening.
≥ 1 PsA-related hand and/or foot joint erosion on X-ray during Screening Period that is confirmed by central reading.
Must have completed the week 52 treatment for the optional open-label long-term extension period.
Exclusion Criteria
Inclusion Criteria
Diagnosed to have psoriatic arthritis (PsA) of at least 3 months duration at screening.
Meets the Classification Criteria for Psoriatic Arthritis at Screening.
Active plaque psoriatic skin lesion(s) or documented medical history of plaque psoriasis (PsO) at screening.
Active arthritis as shown by ≥ 3 swollen joints and ≥ 3 tender joints at Screening and day 1.
Participant has high sensitivity C-reactive protein (hsCRP) ≥ 3 mg/L at Screening.
≥ 1 PsA-related hand and/or foot joint erosion on X-ray during Screening Period that is confirmed by central reading.
Must have completed the week 52 treatment for the optional open-label long-term extension period. Exclusion Criteria
Nonplaque psoriasis at screening or day 1.
Other autoimmune condition such as systemic lupus erythematous, mixed connective tissue disease, multiple sclerosis, or vasculitis.
History of or current inflammatory joint disease other than PsA (e.g., gout, reactive arthritis, rheumatoid arthritis, ankylosing spondylitis, Lyme disease).
Active fibromyalgia.
Received an approved or investigational biologic therapy for the treatment of PsA or PsO.
Other protocol-defined Inclusion/Exclusion criteria apply.

Contacts and Locations

Sponsors and CollaboratorsBristol-Myers Squibb
Locations
Local Institution - 0197 | Gilbert Arizona, United States, 85297Local Institution - 0188 | Jonesboro Arkansas, United States, 72401Local Institution - 0168 | Fontana California, United States, 92335Local Institution - 0199 | Fullerton California, United States, 92835Local Institution - 0038 | Sacramento California, United States, 95815Cohen Medical Centers | Thousand Oaks California, United States, 91360Local Institution - 0170 | Denver Colorado, United States, 80230Local Institution - 0195 | Clearwater Florida, United States, 33765Local Institution - 0272 | Margate Florida, United States, 33063Local Institution - 0082 | Miami Lakes Florida, United States, 33014Local Institution - 0171 | Gainesville Georgia, United States, 30501Local Institution - 0087 | Boise Idaho, United States, 83702Local Institution - 0080 | Chicago Illinois, United States, 60640Local Institution - 0177 | Orland Park Illinois, United States, 60467Local Institution - 0178 | Schaumburg Illinois, United States, 60195Local Institution - 0083 | Lexington Kentucky, United States, 40504Local Institution - 0042 | Hagerstown Maryland, United States, 21740Local Institution - 0198 | Detroit Michigan, United States, 48202Local Institution - 0201 | Springfield Missouri, United States, 65807Local Institution - 0268 | Kalispell Montana, United States, 59901Local Institution - 0186 | Voorhees Township New Jersey, United States, 08043University Hospitals Cleveland Medical Center-Dermatology | Cleveland Ohio, United States, 44106Local Institution - 0028 | Middleburg Heights Ohio, United States, 44130Local Institution - 0179 | Perrysburg Ohio, United States, 43551Local Institution - 0182 | Oklahoma City Oklahoma, United States, 73102Local Institution - 0185 | Corvallis Oregon, United States, 97330Local Institution - 0175 | Greenville South Carolina, United States, 29601Local Institution - 0036 | Jackson Tennessee, United States, 38305Local Institution - 0172 | Allen Texas, United States, 75013Local Institution - 0189 | Amarillo Texas, United States, 79124Local Institution - 0032 | Dallas Texas, United States, 75231Local Institution - 0273 | Bothell Washington, United States, 98021Local Institution - 0181 | Beckley West Virginia, United States, 25801Local Institution - 0213 | Ciudad Autónoma de Buenos Aires Buenos Aires, Argentina, 1111Local Institution - 0054 | La Plata Buenos Aires, Argentina, 1900Local Institution - 0215 | Quilmes Buenos Aires, Argentina, 1878Local Institution - 0046 | Córdoba Córdoba Province, Argentina, X5004CDTLocal Institution - 0196 | Rosario Santa Fe Province, Argentina, S2000Local Institution - 0047 | San Miguel de Tucumán Tucumán Province, Argentina, 4000Local Institution - 0194 | Buenos Aires , Argentina, 1426Local Institution - 0169 | Buenos Aires , Argentina, 1428Local Institution - 0192 | Buenos Aires , Argentina, C1427CCLLocal Institution - 0193 | Mendoza , Argentina, 5500Local Institution - 0220 | Phillip Australian Capital Territory, Australia, 2606Local Institution - 0137 | Botany New South Wales, Australia, 2019Local Institution - 0133 | Westmead New South Wales, Australia, 2145Local Institution - 0132 | Woolloongabba Queensland, Australia, 4102Local Institution - 0211 | Hobart Tasmania, Australia, 7000Local Institution - 0136 | Camberwell Victoria, Australia, 3142Local Institution - 0109 | Vitória Espírito Santo, Brazil, 29055450Local Institution - 0001 | Salvador Estado de Bahia, Brazil, 40150-150Local Institution - 0002 | Juiz de Fora Minas Gerais, Brazil, 36010-570Local Institution - 0219 | Curitiba Paraná, Brazil, 80030110Local Institution - 0214 | Curitiba Paraná, Brazil, 80440-080Local Institution - 0005 | Porto Alegre Rio Grande do Sul, Brazil, 90480-000Local Institution - 0108 | Santo André São Paulo, Brazil, 09060-870Local Institution - 0255 | Plovdiv Plovdiv, Bulgaria, 4002Local Institution - 0248 | Sofia Sofia (stolitsa), Bulgaria, 1463Local Institution - 0253 | Burgas , Bulgaria, 8000Local Institution - 0249 | Plovdiv , Bulgaria, 4000Local Institution - 0267 | Plovdiv , Bulgaria, 4000Local Institution - 0246 | Plovdiv , Bulgaria, 4001Local Institution - 0247 | Plovdiv , Bulgaria, 4001Local Institution - 0245 | Sofia , Bulgaria, 1505Local Institution - 0259 | Sofia , Bulgaria, 1784Local Institution - 0250 | Varna , Bulgaria, 9000Local Institution - 0226 | Santiago Santiago Metropolitan, Chile, 0Local Institution - 0099 | Santiago Santiago Metropolitan, Chile, 7500571Local Institution - 0073 | Santiago Santiago Metropolitan, Chile, 7501126Local Institution - 0222 | Santiago Santiago Metropolitan, Chile, 7510047Local Institution - 0111 | Santiago Santiago Metropolitan, Chile, 7640881Local Institution - 0261 | Viña del Mar Valparaiso, Chile, 2531172Local Institution - 0149 | Hefei Anhui, China, 230071Local Institution - 0159 | Beijing Beijing Municipality, China, 100005Local Institution - 0190 | Chongqing Chongqing Municipality, China, 400010Local Institution - 0147 | Guangzhou Guangdong, China, 510120Local Institution - 0143 | Shenzhen Guangdong, China, 518020Local Institution - 0150 | Dalian Liaoning, China, 116000Local Institution - 0146 | Shanghai Shanghai Municipality, China, 200040Local Institution - 0145 | Yiwu Zhejiang, China, 322000Local Institution - 0071 | Bucaramanga Santander Department, Colombia, 680003Local Institution - 0072 | Barranquilla , Colombia, 080020Local Institution - 0069 | Bogotá , Colombia, 110221Local Institution - 0063 | Bogotá , Colombia, 111156Local Institution - 0070 | Cali , Colombia, 760042Local Institution - 0094 | Medellín , Colombia, 050021Local Institution - 0064 | Medellín , Colombia, 050034Local Institution - 0065 | Zipaquirá , Colombia, 250252Local Institution - 0225 | Prague Praha 5, Czechia, 150 06Local Institution - 0269 | Uherské Hradiště Zlín, Czechia, 68601Local Institution - 0202 | Zlín Zlín, Czechia, 760 01Local Institution - 0018 | Ostrava , Czechia, 722 00Local Institution - 0208 | Pardubice , Czechia, 530 02Local Institution - 0097 | Prague , Czechia, 12850Local Institution - 0017 | Prague , Czechia, 130 00Local Institution - 0013 | Helsinki , Finland, 00290Local Institution - 0089 | Kuopio , Finland, 70100Local Institution - 0119 | Turku , Finland, FI-20521Local Institution - 0077 | Chambray-lès-Tours , France, 37170Local Institution - 0075 | Montpellier , France, 34295Local Institution - 0074 | Paris , France, 75010Local Institution - 0270 | Gyula Bekes County, Hungary, 5700Local Institution - 0049 | Székesfehérvár Fejér, Hungary, 8000Local Institution - 0023 | Budapest , Hungary, 1027Local Institution - 0142 | Budapest , Hungary, 1027Local Institution - 0026 | Budapest , Hungary, 1033Local Institution - 0025 | Budapest , Hungary, 1036Local Institution - 0203 | Budapest , Hungary, 1036Local Institution - 0068 | Zalaegerszeg , Hungary, 8900Local Institution - 0104 | Manorhamilton Leitrim, Ireland, F91 X012Local Institution - 0101 | Dublin , Ireland, 4Local Institution - 0102 | Dublin , Ireland, D15 X40DLocal Institution - 0103 | Galway , Ireland, H91 TY80Local Institution - 0066 | Genova , Italy, 16132Local Institution - 0062 | Pavia , Italy, 27100Local Institution - 0096 | Udine , Italy, 33100Local Institution - 0058 | Verona , Italy, 37134Local Institution - 0056 | Saltillo Coahuila, Mexico, 25050Local Institution - 0254 | Guadalajara Jalisco, Mexico, 44610Local Institution - 0057 | Mexico City Mexico City, Mexico, 06720Local Institution - 0128 | San Luis Potosí City San Luis Potosí, Mexico, 78200Local Institution - 0061 | Mérida Yucatán, Mexico, 97070Local Institution - 0212 | Mérida Yucatán, Mexico, 97070Local Institution - 0060 | Chihuahua City , Mexico, 31000Local Institution - 0209 | Mexico City , Mexico, 14080Local Institution - 0095 | Veracruz , Mexico, 91900Local Institution - 0231 | Dąbrówka Greater Poland Voivodeship, Poland, 62-069Local Institution - 0229 | Krakow Lesser Poland Voivodeship, Poland, 30-149Local Institution - 0206 | Nowy Targ Lesser Poland Voivodeship, Poland, 34-400Local Institution - 0244 | Wroclaw Lower Silesian Voivodeship, Poland, 50-381Local Institution - 0232 | Lublin Lublin Voivodeship, Poland, 20-607Local Institution - 0230 | Świdnik Lublin Voivodeship, Poland, 21-040Local Institution - 0233 | Nadarzyn Masovian Voivodeship, Poland, 05-830Local Institution - 0235 | Warsaw Masovian Voivodeship, Poland, 02-665Local Institution - 0243 | Warsaw Masovian Voivodeship, Poland, 02-672Local Institution - 0236 | Wołomin Masovian Voivodeship, Poland, 05-200Local Institution - 0257 | Gdansk Pomeranian Voivodeship, Poland, 80-382Local Institution - 0234 | Gdynia Pomeranian Voivodeship, Poland, 31-338Local Institution - 0241 | Częstochowa Silesian Voivodeship, Poland, 42-202Local Institution - 0252 | Katowice Silesian Voivodeship, Poland, 40-040Local Institution - 0114 | Bialystok , Poland, 15-351Local Institution - 0126 | Krakow , Poland, 30-002Local Institution - 0127 | Krakow , Poland, 30-033Local Institution - 0140 | Krakow , Poland, 31-501Local Institution - 0162 | Olsztyn , Poland, 10-117Local Institution - 0113 | Poznan , Poland, 60-218Local Institution - 0239 | Poznan , Poland, 60-702Local Institution - 0112 | Poznan , Poland, 60-773Local Institution - 0204 | Warsaw , Poland, 00-874Local Institution - 0205 | Warsaw , Poland, 02-118Local Institution - 0125 | Warsaw , Poland, 03-291Local Institution - 0210 | Wroclaw , Poland, 52-210Local Institution - 0238 | Lodz Łódź Voivodeship, Poland, 90-368Local Institution - 0090 | Bucharest Bucharest, Romania, 011172Local Institution - 0266 | Bucharest Bucharest, Romania, 020125Local Institution - 0010 | Râmnicu Vâlcea Vâlcea County, Romania, 247065Local Institution - 0012 | Brasov , Romania, 500283Local Institution - 0167 | Bucharest , Romania, 011025Local Institution - 0260 | Bucharest , Romania, 014142Local Institution - 0263 | Bucharest , Romania, 030463Local Institution - 0184 | Bucharest , Romania, 11057Local Institution - 0011 | Cluj-Napoca , Romania, 400006Local Institution - 0258 | Craiova , Romania, 200347Local Institution - 0262 | Iași , Romania, 700127Local Institution - 0265 | Iași , Romania, 700661Local Institution - 0264 | Iași , Romania, 700714Local Institution - 0091 | Timișoara , Romania, 300778Local Institution | Kemerovo , Russia, 650070Local Institution | Korolyov , Russia, 141060Local Institution | Saint Petersburg , Russia, 194214Local Institution | Yaroslavl , Russia, 150003Local Institution - 0021 | A Coruña , Spain, 15006Local Institution - 0022 | Córdoba , Spain, 14004Local Institution - 0019 | Madrid , Spain, 28046Local Institution - 0020 | Sabadell , Spain, 08208Local Institution - 0123 | Kaohsiung City , Taiwan, 833401Local Institution - 0121 | Tainan , Taiwan, 704Local Institution - 0122 | Tainan , Taiwan, 710Local Institution - 0120 | Taipei , Taiwan, 110Local Institution - 0124 | Taoyuan , Taiwan, 333423Local Institution - 0106 | Southampton Hampshire, United Kingdom, SO16 6YDLocal Institution - 0116 | Harlow , United Kingdom, CM227NRLocal Institution - 0107 | Stoke-on-Trent , United Kingdom, ST6 7AG
Investigators
Study Director: Bristol-Myers Squibb, Bristol-Myers Squibb
Study Documents (Full Text)
Documents provided by Bristol-Myers SquibbStudy Protocol and Statistical Analysis Plan  May 5, 2024