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Un estudio para determinar la eficacia y la seguridad de deucravacitinib en comparación con un placebo en participantes con artritis psoriásica activa (PsA) que nunca han recibido fármacos antirreumáticos biológicos modificadores de la enfermedad

24 de septiembre de 2026 actualizado por: Bristol-Myers Squibb

Un estudio de fase 3, aleatorizado, doble ciego, controlado con placebo para evaluar la eficacia y la seguridad de deucravacitinib en participantes con artritis psoriásica activa que nunca han recibido fármacos antirreumáticos modificadores biológicos de la enfermedad

The purpose of this study is to evaluate the efficacy and safety of deucravacitinib versus placebo in participants with active psoriatic arthritis who are naïve to biologic disease-modifying anti-rheumatic drugs. The long term extension period will provide additional long-term efficacy and safety information.

Descripción general del estudio

Estado

Activo, no reclutando

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Actual)

670

Fase

  • Fase 3

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

  • Argentina
      • Buenos Aires, Argentina, 1426
        • Local Institution - 0194
      • Buenos Aires, Argentina, 1428
        • Local Institution - 0169
      • Buenos Aires, Argentina, C1427CCL
        • Local Institution - 0192
      • Mendoza, Argentina, 5500
        • Local Institution - 0193
    • Buenos Aires
      • Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina, 1111
        • Local Institution - 0213
      • La Plata, Buenos Aires, Argentina, 1900
        • Local Institution - 0054
      • Quilmes, Buenos Aires, Argentina, 1878
        • Local Institution - 0215
    • Córdoba Province
      • Córdoba, Córdoba Province, Argentina, X5004CDT
        • Local Institution - 0046
    • Santa Fe Province
      • Rosario, Santa Fe Province, Argentina, S2000
        • Local Institution - 0196
    • Tucumán Province
      • San Miguel de Tucumán, Tucumán Province, Argentina, 4000
        • Local Institution - 0047
  • Australia
    • Australian Capital Territory
      • Phillip, Australian Capital Territory, Australia, 2606
        • Local Institution - 0220
    • New South Wales
      • Botany, New South Wales, Australia, 2019
        • Local Institution - 0137
      • Westmead, New South Wales, Australia, 2145
        • Local Institution - 0133
    • Queensland
      • Woolloongabba, Queensland, Australia, 4102
        • Local Institution - 0132
    • Tasmania
      • Hobart, Tasmania, Australia, 7000
        • Local Institution - 0211
    • Victoria
      • Camberwell, Victoria, Australia, 3142
        • Local Institution - 0136
  • Brasil
    • Espírito Santo
      • Vitória, Espírito Santo, Brasil, 29055450
        • Local Institution - 0109
    • Estado de Bahia
      • Salvador, Estado de Bahia, Brasil, 40150-150
        • Local Institution - 0001
    • Minas Gerais
      • Juiz de Fora, Minas Gerais, Brasil, 36010-570
        • Local Institution - 0002
    • Paraná
      • Curitiba, Paraná, Brasil, 80030110
        • Local Institution - 0219
      • Curitiba, Paraná, Brasil, 80440-080
        • Local Institution - 0214
    • Rio Grande do Sul
      • Porto Alegre, Rio Grande do Sul, Brasil, 90480-000
        • Local Institution - 0005
    • São Paulo
      • Santo André, São Paulo, Brasil, 09060-870
        • Local Institution - 0108
  • Bulgaria
      • Burgas, Bulgaria, 8000
        • Local Institution - 0253
      • Plovdiv, Bulgaria, 4000
        • Local Institution - 0249
      • Plovdiv, Bulgaria, 4000
        • Local Institution - 0267
      • Plovdiv, Bulgaria, 4001
        • Local Institution - 0246
      • Plovdiv, Bulgaria, 4001
        • Local Institution - 0247
      • Sofia, Bulgaria, 1505
        • Local Institution - 0245
      • Sofia, Bulgaria, 1784
        • Local Institution - 0259
      • Varna, Bulgaria, 9000
        • Local Institution - 0250
    • Plovdiv
      • Plovdiv, Plovdiv, Bulgaria, 4002
        • Local Institution - 0255
    • Sofia (stolitsa)
      • Sofia, Sofia (stolitsa), Bulgaria, 1463
        • Local Institution - 0248
  • Chequia
      • Ostrava, Chequia, 722 00
        • Local Institution - 0018
      • Pardubice, Chequia, 530 02
        • Local Institution - 0208
      • Prague, Chequia, 12850
        • Local Institution - 0097
      • Prague, Chequia, 130 00
        • Local Institution - 0017
    • Praha 5
      • Prague, Praha 5, Chequia, 150 06
        • Local Institution - 0225
    • Zlín
      • Uherské Hradiště, Zlín, Chequia, 68601
        • Local Institution - 0269
      • Zlín, Zlín, Chequia, 760 01
        • Local Institution - 0202
  • Chile
    • Santiago Metropolitan
      • Santiago, Santiago Metropolitan, Chile
        • Local Institution - 0226
      • Santiago, Santiago Metropolitan, Chile, 7500571
        • Local Institution - 0099
      • Santiago, Santiago Metropolitan, Chile, 7501126
        • Local Institution - 0073
      • Santiago, Santiago Metropolitan, Chile, 7510047
        • Local Institution - 0222
      • Santiago, Santiago Metropolitan, Chile, 7640881
        • Local Institution - 0111
    • Valparaiso
      • Viña del Mar, Valparaiso, Chile, 2531172
        • Local Institution - 0261
  • Colombia
      • Barranquilla, Colombia, 080020
        • Local Institution - 0072
      • Bogotá, Colombia, 110221
        • Local Institution - 0069
      • Bogotá, Colombia, 111156
        • Local Institution - 0063
      • Cali, Colombia, 760042
        • Local Institution - 0070
      • Medellín, Colombia, 050021
        • Local Institution - 0094
      • Medellín, Colombia, 050034
        • Local Institution - 0064
      • Zipaquirá, Colombia, 250252
        • Local Institution - 0065
    • Santander Department
      • Bucaramanga, Santander Department, Colombia, 680003
        • Local Institution - 0071
  • España
      • A Coruña, España, 15006
        • Local Institution - 0021
      • Córdoba, España, 14004
        • Local Institution - 0022
      • Madrid, España, 28046
        • Local Institution - 0019
      • Sabadell, España, 08208
        • Local Institution - 0020
  • Estados Unidos
    • Arizona
      • Gilbert, Arizona, Estados Unidos, 85297
        • Local Institution - 0197
    • Arkansas
      • Jonesboro, Arkansas, Estados Unidos, 72401
        • Local Institution - 0188
    • California
      • Fontana, California, Estados Unidos, 92335
        • Local Institution - 0168
      • Fullerton, California, Estados Unidos, 92835
        • Local Institution - 0199
      • Sacramento, California, Estados Unidos, 95815
        • Local Institution - 0038
      • Thousand Oaks, California, Estados Unidos, 91360
        • Cohen Medical Centers
    • Colorado
      • Denver, Colorado, Estados Unidos, 80230
        • Local Institution - 0170
    • Florida
      • Clearwater, Florida, Estados Unidos, 33765
        • Local Institution - 0195
      • Margate, Florida, Estados Unidos, 33063
        • Local Institution - 0272
      • Miami Lakes, Florida, Estados Unidos, 33014
        • Local Institution - 0082
    • Georgia
      • Gainesville, Georgia, Estados Unidos, 30501
        • Local Institution - 0171
    • Idaho
      • Boise, Idaho, Estados Unidos, 83702
        • Local Institution - 0087
    • Illinois
      • Chicago, Illinois, Estados Unidos, 60640
        • Local Institution - 0080
      • Orland Park, Illinois, Estados Unidos, 60467
        • Local Institution - 0177
      • Schaumburg, Illinois, Estados Unidos, 60195
        • Local Institution - 0178
    • Kentucky
      • Lexington, Kentucky, Estados Unidos, 40504
        • Local Institution - 0083
    • Maryland
      • Hagerstown, Maryland, Estados Unidos, 21740
        • Local Institution - 0042
    • Michigan
      • Detroit, Michigan, Estados Unidos, 48202
        • Local Institution - 0198
    • Missouri
      • Springfield, Missouri, Estados Unidos, 65807
        • Local Institution - 0201
    • Montana
      • Kalispell, Montana, Estados Unidos, 59901
        • Local Institution - 0268
    • New Jersey
      • Voorhees Township, New Jersey, Estados Unidos, 08043
        • Local Institution - 0186
    • Ohio
      • Cleveland, Ohio, Estados Unidos, 44106
        • University Hospitals Cleveland Medical Center-Dermatology
      • Middleburg Heights, Ohio, Estados Unidos, 44130
        • Local Institution - 0028
      • Perrysburg, Ohio, Estados Unidos, 43551
        • Local Institution - 0179
    • Oklahoma
      • Oklahoma City, Oklahoma, Estados Unidos, 73102
        • Local Institution - 0182
    • Oregon
      • Corvallis, Oregon, Estados Unidos, 97330
        • Local Institution - 0185
    • South Carolina
      • Greenville, South Carolina, Estados Unidos, 29601
        • Local Institution - 0175
    • Tennessee
      • Jackson, Tennessee, Estados Unidos, 38305
        • Local Institution - 0036
    • Texas
      • Allen, Texas, Estados Unidos, 75013
        • Local Institution - 0172
      • Amarillo, Texas, Estados Unidos, 79124
        • Local Institution - 0189
      • Dallas, Texas, Estados Unidos, 75231
        • Local Institution - 0032
    • Washington
      • Bothell, Washington, Estados Unidos, 98021
        • Local Institution - 0273
    • West Virginia
      • Beckley, West Virginia, Estados Unidos, 25801
        • Local Institution - 0181
  • Finlandia
      • Helsinki, Finlandia, 00290
        • Local Institution - 0013
      • Kuopio, Finlandia, 70100
        • Local Institution - 0089
      • Turku, Finlandia, FI-20521
        • Local Institution - 0119
  • Francia
      • Chambray-lès-Tours, Francia, 37170
        • Local Institution - 0077
      • Montpellier, Francia, 34295
        • Local Institution - 0075
      • Paris, Francia, 75010
        • Local Institution - 0074
  • Hungría
      • Budapest, Hungría, 1027
        • Local Institution - 0023
      • Budapest, Hungría, 1027
        • Local Institution - 0142
      • Budapest, Hungría, 1033
        • Local Institution - 0026
      • Budapest, Hungría, 1036
        • Local Institution - 0025
      • Budapest, Hungría, 1036
        • Local Institution - 0203
      • Zalaegerszeg, Hungría, 8900
        • Local Institution - 0068
    • Bekes County
      • Gyula, Bekes County, Hungría, 5700
        • Local Institution - 0270
    • Fejér
      • Székesfehérvár, Fejér, Hungría, 8000
        • Local Institution - 0049
  • Irlanda
      • Dublin, Irlanda, 4
        • Local Institution - 0101
      • Dublin, Irlanda, D15 X40D
        • Local Institution - 0102
      • Galway, Irlanda, H91 TY80
        • Local Institution - 0103
    • Leitrim
      • Manorhamilton, Leitrim, Irlanda, F91 X012
        • Local Institution - 0104
  • Italia
      • Genova, Italia, 16132
        • Local Institution - 0066
      • Pavia, Italia, 27100
        • Local Institution - 0062
      • Udine, Italia, 33100
        • Local Institution - 0096
      • Verona, Italia, 37134
        • Local Institution - 0058
  • México
      • Chihuahua City, México, 31000
        • Local Institution - 0060
      • Mexico City, México, 14080
        • Local Institution - 0209
      • Veracruz, México, 91900
        • Local Institution - 0095
    • Coahuila
      • Saltillo, Coahuila, México, 25050
        • Local Institution - 0056
    • Jalisco
      • Guadalajara, Jalisco, México, 44610
        • Local Institution - 0254
    • Mexico City
      • Mexico City, Mexico City, México, 06720
        • Local Institution - 0057
    • San Luis Potosí
      • San Luis Potosí City, San Luis Potosí, México, 78200
        • Local Institution - 0128
    • Yucatán
      • Mérida, Yucatán, México, 97070
        • Local Institution - 0061
      • Mérida, Yucatán, México, 97070
        • Local Institution - 0212
  • Polonia
      • Bialystok, Polonia, 15-351
        • Local Institution - 0114
      • Krakow, Polonia, 31-501
        • Local Institution - 0140
      • Krakow, Polonia, 30-002
        • Local Institution - 0126
      • Krakow, Polonia, 30-033
        • Local Institution - 0127
      • Olsztyn, Polonia, 10-117
        • Local Institution - 0162
      • Poznan, Polonia, 60-218
        • Local Institution - 0113
      • Poznan, Polonia, 60-773
        • Local Institution - 0112
      • Poznan, Polonia, 60-702
        • Local Institution - 0239
      • Warsaw, Polonia, 00-874
        • Local Institution - 0204
      • Warsaw, Polonia, 02-118
        • Local Institution - 0205
      • Warsaw, Polonia, 03-291
        • Local Institution - 0125
      • Wroclaw, Polonia, 52-210
        • Local Institution - 0210
    • Greater Poland Voivodeship
      • Dąbrówka, Greater Poland Voivodeship, Polonia, 62-069
        • Local Institution - 0231
    • Lesser Poland Voivodeship
      • Krakow, Lesser Poland Voivodeship, Polonia, 30-149
        • Local Institution - 0229
      • Nowy Targ, Lesser Poland Voivodeship, Polonia, 34-400
        • Local Institution - 0206
    • Lower Silesian Voivodeship
      • Wroclaw, Lower Silesian Voivodeship, Polonia, 50-381
        • Local Institution - 0244
    • Lublin Voivodeship
      • Lublin, Lublin Voivodeship, Polonia, 20-607
        • Local Institution - 0232
      • Świdnik, Lublin Voivodeship, Polonia, 21-040
        • Local Institution - 0230
    • Masovian Voivodeship
      • Nadarzyn, Masovian Voivodeship, Polonia, 05-830
        • Local Institution - 0233
      • Warsaw, Masovian Voivodeship, Polonia, 02-665
        • Local Institution - 0235
      • Warsaw, Masovian Voivodeship, Polonia, 02-672
        • Local Institution - 0243
      • Wołomin, Masovian Voivodeship, Polonia, 05-200
        • Local Institution - 0236
    • Pomeranian Voivodeship
      • Gdansk, Pomeranian Voivodeship, Polonia, 80-382
        • Local Institution - 0257
      • Gdynia, Pomeranian Voivodeship, Polonia, 31-338
        • Local Institution - 0234
    • Silesian Voivodeship
      • Częstochowa, Silesian Voivodeship, Polonia, 42-202
        • Local Institution - 0241
      • Katowice, Silesian Voivodeship, Polonia, 40-040
        • Local Institution - 0252
    • Łódź Voivodeship
      • Lodz, Łódź Voivodeship, Polonia, 90-368
        • Local Institution - 0238
  • Porcelana
    • Anhui
      • Hefei, Anhui, Porcelana, 230071
        • Local Institution - 0149
    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana, 100005
        • Local Institution - 0159
    • Chongqing Municipality
      • Chongqing, Chongqing Municipality, Porcelana, 400010
        • Local Institution - 0190
    • Guangdong
      • Guangzhou, Guangdong, Porcelana, 510120
        • Local Institution - 0147
      • Shenzhen, Guangdong, Porcelana, 518020
        • Local Institution - 0143
    • Liaoning
      • Dalian, Liaoning, Porcelana, 116000
        • Local Institution - 0150
    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Porcelana, 200040
        • Local Institution - 0146
    • Zhejiang
      • Yiwu, Zhejiang, Porcelana, 322000
        • Local Institution - 0145
  • Reino Unido
      • Harlow, Reino Unido, CM227NR
        • Local Institution - 0116
      • Stoke-on-Trent, Reino Unido, ST6 7AG
        • Local Institution - 0107
    • Hampshire
      • Southampton, Hampshire, Reino Unido, SO16 6YD
        • Local Institution - 0106
  • Rumania
      • Brasov, Rumania, 500283
        • Local Institution - 0012
      • Bucharest, Rumania, 011025
        • Local Institution - 0167
      • Bucharest, Rumania, 030463
        • Local Institution - 0263
      • Bucharest, Rumania, 11057
        • Local Institution - 0184
      • Bucharest, Rumania, 014142
        • Local Institution - 0260
      • Cluj-Napoca, Rumania, 400006
        • Local Institution - 0011
      • Craiova, Rumania, 200347
        • Local Institution - 0258
      • Iași, Rumania, 700127
        • Local Institution - 0262
      • Iași, Rumania, 700661
        • Local Institution - 0265
      • Iași, Rumania, 700714
        • Local Institution - 0264
      • Timișoara, Rumania, 300778
        • Local Institution - 0091
    • Bucharest
      • Bucharest, Bucharest, Rumania, 011172
        • Local Institution - 0090
      • Bucharest, Bucharest, Rumania, 020125
        • Local Institution - 0266
    • Vâlcea County
      • Râmnicu Vâlcea, Vâlcea County, Rumania, 247065
        • Local Institution - 0010
  • Rusia
      • Kemerovo, Rusia, 650070
        • Local Institution
      • Korolyov, Rusia, 141060
        • Local Institution
      • Saint Petersburg, Rusia, 194214
        • Local Institution
      • Yaroslavl, Rusia, 150003
        • Local Institution
  • Taiwán
      • Kaohsiung City, Taiwán, 833401
        • Local Institution - 0123
      • Tainan, Taiwán, 704
        • Local Institution - 0121
      • Tainan, Taiwán, 710
        • Local Institution - 0122
      • Taipei, Taiwán, 110
        • Local Institution - 0120
      • Taoyuan, Taiwán, 333423
        • Local Institution - 0124

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador de placebos: Placebo
Otro: Placebo

Specified dose on specified days
Experimental: Deucravacitinib
Droga: Deucravacitinib

Specified dose on specified days

Otros nombres:
  • BMS-986165

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Percentage of Participants With ACR 20 Response at Week 16
Periodo de tiempo: 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.
Week 16

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change From Baseline in Disease Activity Score 28 C-reactive Protein (DAS28-CRP) at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and Week 16
Change From Baseline in Health Assessment Questionnaire - Disability Index (HAQ-DI) at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and Week 16
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
Periodo de tiempo: Week 16

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.
Week 16
Change From Baseline in the 36-item Short Form (SF-36) Physical Subcomponent Summary (PCS) Score at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and Week 16
Percentage of Participants Meeting Enthesitis Resolution (Score of 0) Among Participants With Enthesitis at Baseline by Leeds Enthesitis Index (LEI) at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Minimal Disease Activity (MDA) at Week 16
Periodo de tiempo: 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
Week 16
Change From Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-Fatigue) Score at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and Week 16
Percentage of Participants Meeting Dactylitis Resolution at Week 16
Periodo de tiempo: 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.
Week 16
Change From Baseline in PsA-modified Sharp-van Der Heijde (SvdH) Score at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and Week 16
Percentage of Participants With ACR 20 Response up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12, and 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.
Week 2, 4, 8, 12, and 16
Percentage of Participants With ACR 50 Response up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12, and 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.
Week 2, 4, 8, 12, and 16
Percentage of Participants With ACR 70 Response up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12, and 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.
Week 2, 4, 8, 12, and 16
Change From Baseline in Health Assessment Questionnaire - Disability Index (HAQ-DI) up to Week 16
Periodo de tiempo: Baseline and Week 2, 4, 8, 12, and 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.
Baseline and Week 2, 4, 8, 12, and 16
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
Periodo de tiempo: Baseline and Week 2, 4, 8, 12, and 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. Clinically meaningful improvement was defined as ≥0.35improvement from baseline.
Baseline and Week 2, 4, 8, 12, and 16
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
Periodo de tiempo: Week 4, 8, 12 and 16

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.
Week 4, 8, 12 and 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
Periodo de tiempo: Week 4, 8, 12 and 16

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.
Week 4, 8, 12 and 16
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
Periodo de tiempo: Week 4, 8, 12 and 16

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.
Week 4, 8, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) Physical Subcomponent Summary (PCS) Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Percentage of Participants Meeting Enthesitis Resolution (Score of 0) Among Participants With Enthesitis at Baseline by Leeds Enthesitis Index (LEI) up to Week 16
Periodo de tiempo: Week 4, 8, 12 and 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.
Week 4, 8, 12 and 16
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
Periodo de tiempo: Week 4, 8, 12 and 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.
Week 4, 8, 12 and 16
Percentage of Participants Meeting Achievement of Minimal Disease Activity (MDA) up to Week 16
Periodo de tiempo: Week 4, 8, 12, and 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
Week 4, 8, 12, and 16
Change From Baseline in the 36-item Short Form (SF-36) Mental Component Summary (MCS) Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-Fatigue) Score up to Week 16
Periodo de tiempo: Baseline and Week 2, 4, 8, 12 and 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.
Baseline and Week 2, 4, 8, 12 and 16
Percentage of Participants Meeting Dactylitis Resolution up to Week 16
Periodo de tiempo: Week 4, 8, 12 and 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.
Week 4, 8, 12 and 16
Change From Baseline in Psoriatic Arthritis Impact of Disease (PsAID) 12 Score up to Week 16
Periodo de tiempo: Baseline and Week 2, 4, 8, 12 and 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.
Baseline and Week 2, 4, 8, 12 and 16
Change From Baseline in Disease Activity Index for Psoriatic Arthritis (DAPSA) Score up to Week 16
Periodo de tiempo: Baseline and Week 2, 4, 8, 12 and 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.
Baseline and Week 2, 4, 8, 12 and 16
Percentage of Participants With Achievement of Disease Activity Index for Psoriatic Arthritis (DAPSA) Low Disease Activity Response up to Week 16
Periodo de tiempo: Baseline and Week 2, 4, 8, 12 and 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.
Baseline and Week 2, 4, 8, 12 and 16
Percentage of Participants With Achievement of Disease Activity Index for Psoriatic Arthritis (DAPSA) Disease Remission up to Week 16
Periodo de tiempo: Baseline and Week 2, 4, 8, 12 and 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.
Baseline and Week 2, 4, 8, 12 and 16
Percentage of Participants Meeting Achievement of Physician Global Assessment-Fingernails (PGA-F) of 0/1 up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12 and 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.
Week 2, 4, 8, 12 and 16
Change From Baseline in Disease Activity Score 28 C-reactive Protein (DAS28-CRP) up to Week 16
Periodo de tiempo: Baseline and Week 2, 4, 8, 12 and 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.
Baseline and Week 2, 4, 8, 12 and 16
Percentage of Participants Meeting Disease Activity Score 28 C-reactive Protein (DAS28-CRP) Low Disease Activity Response up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12 and 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.
Week 2, 4, 8, 12 and 16
Percentage of Participants Meeting Disease Activity Score 28 C-reactive Protein (DAS28-CRP) Disease Remission up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12 and 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.
Week 2, 4, 8, 12 and 16
Change From Baseline in Psoriatic Arthritis Disease Activity Score (PASDAS) up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in Modified Composite Psoriatic Disease Activity Index (mCPDAI) up to Week 16
Periodo de tiempo: Baseline and Week 4, 8, 12 and 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.
Baseline and Week 4, 8, 12 and 16
Percentage of Participants With Achievement of Psoriatic Arthritis Response Criteria (PsARC) up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12 and 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
Week 2, 4, 8, 12 and 16
Percentage of Participants Meeting Achievement of Improvement of Bath Ankylosing Spondylitis Disease Activity (BASDAI) Score up to Week 16
Periodo de tiempo: Week 2, 4, 8, 12 and 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
Week 2, 4, 8, 12 and 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Scores Response of <= 0 at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Scores Response of <= 0.5 at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Scores Response of <= Smallest Detectable Change (SDC) at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Erosion Scores Response of <= 0 at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Erosion Scores Response of <= 0.5 at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Erosion Scores Response of <= SDC at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Joint Space Narrowing (JSN) Scores Response of <= 0 at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Joint Space Narrowing (JSN) Scores Response of <= 0.5 at Week 16
Periodo de tiempo: 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.
Week 16
Percentage of Participants Meeting Achievement of Total PsA-modified SvdH Joint Space Narrowing (JSN) Scores Response of <= SDC at Week 16
Periodo de tiempo: 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.
Week 16
Change From Baseline in PsA-modified SvdH Erosion Scores Response at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and Week 16
Change From Baseline in PsA-modified SvdH JSN Scores Response at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and Week 16
Change From Baseline in the 36-item Short Form (SF-36) Physical Subcomponent Summary Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) Role Activity Subcomponent Summary Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) Bodily Pain Subcomponent Summary Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) General Health Perceptions Subcomponent Summary Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) Vitality Subcomponent Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) Social Subcomponent Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) Mental Health Subcomponent Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the 36-item Short Form (SF-36) Emotional Problems Subcomponent Score up to Week 16
Periodo de tiempo: Baseline and Week 4, 12 and 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.
Baseline and Week 4, 12 and 16
Change From Baseline in the Work Productivity and Activity Impairment (WPAI) Subcomponents Score at Week 16
Periodo de tiempo: Baseline and 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.
Baseline and week 16
Change From Baseline in the European Quality of Life 5D-5L (EQ-5D-5L) Utility Scores and Its Subcomponents up to 16
Periodo de tiempo: Baseline and week 4 and 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 '1' indicates no problem, and '5' 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.
Baseline and week 4 and 16
Change From Baseline in Patient-Reported Outcome Measures Information System (PROMIS) Sleep Disturbance up to Week 16
Periodo de tiempo: Baseline and week 4, 12, and 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 = "not at all" to 5 = "very much" 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.
Baseline and week 4, 12, and 16

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Bristol-Myers Squibb

Investigadores

  • Director de estudio: Bristol-Myers Squibb, Bristol-Myers Squibb

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Enlaces Útiles

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

13 de julio de 2021

Finalización primaria (Actual)

10 de octubre de 2024

Finalización del estudio (Estimado)

3 de junio de 2027

Fechas de registro del estudio

Enviado por primera vez

28 de mayo de 2021

Primero enviado que cumplió con los criterios de control de calidad

28 de mayo de 2021

Publicado por primera vez (Actual)

1 de junio de 2021

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

16 de octubre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

24 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Palabras clave

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • IM011-054
  • U1111-1259-9443 (Identificador de registro: WHO)
  • 2023-506256-25 (Otro identificador: EU Trial Number)
  • 2023 (Subvención/contrato del NIH de EE. UU.)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

BMS will provide access to individual anonymized participant data upon request from qualified researchers, and subject to certain criteria. Additional information regarding Bristol Myer Squibb's data sharing policy and process can be found at https://www.bms.com/researchers-and-partners/clinical-trials-and-research.html

Marco de tiempo para compartir IPD

See Plan Description

Criterios de acceso compartido de IPD

See Plan Description

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • RSC

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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