MedPath

A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic Arthritis (PsA) Who Have a History of Inadequate Response to or Intolerance to at Least One Disease Modifying Anti-Rheumatic Drug (DMARD) Therapy

Phase 3
Active, not recruiting
Conditions
Psoriatic Arthritis
Interventions
Biological: Placebo
Biological: Risankizumab
Registration Number
NCT03675308
Lead Sponsor
AbbVie
Brief Summary

The purpose of this study is to compare the safety and efficacy of risankizumab versus placebo in participants with moderately to severely active psoriatic arthritis (PsA).

Detailed Description

The study consists of a Screening Period (approximately 35 days), Period 1, Period 2, and a 20-week Follow-up Period. Period 1 is a 24-week randomized, double-blind, placebo-controlled, parallel-group treatment period. Period 2 is the long-term treatment period and starts at Week 24. To maintain the blind to the original treatment allocation, treatment at the Week 24 Visit is blinded: participants randomized to placebo receive blinded risankizumab 150 mg, and participants randomized to risankizumab receive blinded placebo. At Week 28 and for the remaining dosing visits (to Week 316), all participants are to receive open-label risankizumab 150 mg every 12 weeks. Participants will remain blinded to the original randomization allocation for the duration of the study. The total study duration is 336 weeks including a telephone call 140 days (20 weeks) after last dose of study drug.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
964
Inclusion Criteria
  • Clinical diagnosis of PsA with symptom onset at least 6 months prior to the Screening Visit and fulfillment of the Classification Criteria for PsA (CASPAR) at the Screening Visit.

  • Participant has active disease at Baseline defined as ≥ 5 tender joints (based on 68 joint counts) and ≥ 5 swollen joints (based on 66 joint counts)

  • Diagnosis of active plaque psoriasis with at least one psoriatic plaque of ≥ 2 cm diameter or nail changes consistent with psoriasis at Screening Visit.

  • Participant has demonstrated an inadequate response or intolerance to or contraindication for conventional synthetic disease modifying anti-rheumatic drugs (csDMARD) therapy(ies).

  • Presence of either at Screening:

    • ≥ 1 erosion on radiograph as determined by central imaging review or;
    • High sensitivity C-reactive protein (hsCRP) ≥ 3.0 mg/L.
Read More
Exclusion Criteria
  • Participant is considered by investigator, for any reason, to be an unsuitable candidate for the study.
  • Participant has a known hypersensitivity to risankizumab.
  • Participant has previous treatment with biologic agent.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RisankizumabPlaceboParticipants randomized to receive 150 mg risankizumab administered by subcutaneous injection at Week 0, Week 4, and Week 16 in Period 1. At Week 24 participants will receive blinded placebo followed by open-label 150 mg risankizumab at Week 28, and every 12 weeks thereafter in Period 2 until the final dosing time point at Week 316.
PlaceboPlaceboParticipants randomized to receive double-blind placebo at Week 0, Week 4, and Week 16 in Period 1. At Week 24 participants will receive 150 mg risankizumab followed by open-label 150 mg risankizumab at Week 28, and every 12 weeks thereafter in Period 2 until the final dosing time point at Week 316.
PlaceboRisankizumabParticipants randomized to receive double-blind placebo at Week 0, Week 4, and Week 16 in Period 1. At Week 24 participants will receive 150 mg risankizumab followed by open-label 150 mg risankizumab at Week 28, and every 12 weeks thereafter in Period 2 until the final dosing time point at Week 316.
RisankizumabRisankizumabParticipants randomized to receive 150 mg risankizumab administered by subcutaneous injection at Week 0, Week 4, and Week 16 in Period 1. At Week 24 participants will receive blinded placebo followed by open-label 150 mg risankizumab at Week 28, and every 12 weeks thereafter in Period 2 until the final dosing time point at Week 316.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 24Baseline and Week 24

Participants who met the following 3 conditions for improvement from Baseline were classified as meeting the ACR20 response criteria:

1. ≥ 20% improvement in 68-tender joint count;

2. ≥ 20% improvement in 66-swollen joint count; and

3. ≥ 20% improvement in at least 3 of the 5 following parameters:

* Physician global assessment of disease activity

* Patient global assessment of disease activity

* Patient assessment of pain

* Health Assessment Questionnaire - Disability Index (HAQ-DI)

* High-sensitivity C-reactive protein (hsCRP).

Secondary Outcome Measures
NameTimeMethod
Percentage of Participants With an ACR20 Response at Week 16Baseline and Week 16

Participants who met the following 3 conditions for improvement from Baseline were classified as meeting the ACR20 response criteria:

1. ≥ 20% improvement in 68-tender joint count;

2. ≥ 20% improvement in 66-swollen joint count; and

3. ≥ 20% improvement in at least 3 of the 5 following parameters:

* Physician global assessment of disease activity

* Patient global assessment of disease activity

* Patient assessment of pain

* Health Assessment Questionnaire - Disability Index (HAQ-DI)

* High-sensitivity C-reactive protein (hsCRP).

Change From Baseline In 36-Item Short Form Health Survey (SF-36) Physical Component Summary (PCS) Score at Week 24Baseline and Week 24

The Short Form 36-Item Health Survey (SF-36) Version 2 is a self-administered questionnaire that measures the impact of disease on overall quality of life during the past 4 weeks. The SF-36 consists of 36 questions in eight domains (physical function, pain, general and mental health, vitality, social function, physical and emotional health).

The physical component summary is a weighted combination of the 8 subscales with positive weighting for physical functioning, role-physical, bodily pain, and general health. The SF-36 PCS ranges from 0 to 100. A linear algorithm was applied to the calculation of the PCS which has a normative mean value of 50. Higher scores are associated with less disability; a score of 100 is equivalent to no disability and a score of 0 is equivalent to maximum disability. A positive change from Baseline score indicates improvement.

Change From Baseline In Health Assessment Questionnaire-Disability Index (HAQ-DI) at Week 24Baseline and Week 24

The Health Assessment Questionnaire Disability Index is a patient-reported questionnaire that measures the degree of difficulty a person has in accomplishing tasks in 8 functional areas (dressing, arising, eating, walking, hygiene, reaching, gripping, and errands and chores) over the past week. Participants assessed their ability to do each task on a scale from 0 (without any difficulty) to 3 (unable to do). Scores were averaged to provide an overall score ranging from 0 to 3, where 0 represents no disability and 3 represents very severe, high-dependency disability.

A negative change from Baseline in the overall score indicates improvement.

Percentage of Participants Achieving Psoriasis Area Severity Index (PASI) 90 Response at Week 24Baseline and Week 24

PASI is a composite score based on the percentage of the body surface area (BSA) affected by psoriasis and the intensity of erythema (reddening), induration (thickening or hardening of the skin), and desquamation (peeling of the skin) of lesions assessed at 4 anatomic sites (head, upper extremities, trunk, and lower extremities). At each location, the percentage of BSA involvement is assigned a score from 0 (no involvement) to 6 (90% to 100% involvement), and erythema, induration, and desquamation are scored on a scale from 0 (no symptoms) to 4 (very marked).

The PASI score ranges from 0 (no psoriasis) to 72 (very severe psoriasis). A PASI 90 response is the percentage of participants who achieved at least a 90% reduction (improvement) from Baseline in PASI score.

Percentage of Participants With Resolution of Enthesitis at Week 24Week 24

Resolution of enthesitis is defined as a Leeds Enthesitis Index (LEI) score = 0.

LEI is an enthesitis measure developed specifically for PsA and assesses the presence or absence of tenderness at the following 3 bilateral enthesial sites: medial femoral condyles, lateral epicondyles of the humerus, and Achilles tendon insertions. Tenderness on examination is recorded as either present (coded as 1), absent (coded as 0), or not assessed for each of the 6 sites. The LEI is calculated by taking the sum of the scores from the 6 sites. The LEI ranges from 0 to 6 (worst).

To increase the sample size due to the smaller number of participants with enthesitis at Baseline, the pre-specified analysis of the resolution of enthesitis included pooled data from KEEPsAKE 1 (this study) and the companion study KEEPsAKE 2 (M15-998; NCT03671148).

Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 24Baseline and Week 24

Participants who met the following 3 conditions for improvement from Baseline were classified as meeting the ACR50 response criteria:

1. ≥ 50% improvement in 68-tender joint count;

2. ≥ 50% improvement in 66-swollen joint count; and

3. ≥ 50% improvement in at least 3 of the 5 following parameters:

* Physician global assessment of disease activity

* Patient global assessment of disease activity

* Patient assessment of pain

* Health Assessment Questionnaire - Disability Index (HAQ-DI)

* High-sensitivity C-reactive protein (hsCRP).

Percentage of Participants Achieving Minimal Disease Activity (MDA) at Week 24Week 24

A participant was classified as achieving MDA if 5 of the following 7 criteria were met:

* Tender joint count (out of 68 joints) ≤ 1

* Swollen joint count (out of 66 joints) ≤ 1

* PASI score ≤ 1 (score ranges from 0 - 72) or percent BSA involved with psoriasis ≤ 3%

* Patient's assessment of pain ≤ 15 (VAS from 0 to 100)

* Patient's Global Assessment of disease activity ≤ 20 (VAS from 0 to 100)

* HAQ-DI score ≤ 0.5 (index score ranges from 0 to 3)

* Leeds Enthesitis Index ≤ 1 (assesses the presence or absence of enthesitis at 3 bilateral sites, for an overall score range from 0 to 6)

Change From Baseline in Fingernail-Physician Global Assessment (PGA-F)Baseline and Week 24

The PGA-F is a clinician-rated outcomes assessment used to measure the severity of signs and symptoms associated with fingernail psoriasis. Participant's fingernails were assessed separately for nail bed signs and nail matrix signs of disease on a scale from 0 (clear) to 4 (severe). A participant's overall global score is the worse of the nail bed score and nail matrix score. For example, if a participant had a nail bed score '2' and a nail matrix score of '4,' this participant's overall score was '4.' A negative change from Baseline indicates improvement.

Change From Baseline in PsA Modified Total Sharp Score (mTSS) at Week 24Baseline and Week 24

The Sharp-van der Heijde modified scoring method for PsA measures the level of joint damage from radiographs of the hands and feet, and was assessed by 2 independent, blinded readers.

Joint erosion severity was assessed in 20 joints in each hand and wrist and 6 joints in each foot. Each joint was scored from 0 (no erosion) to 5 for hands/wrists or to 10 for feet (complete collapse). The total erosion score ranges from 0 to 320 (worst).

Joint space narrowing (JSN) was assessed in 20 joints of each hand and wrist, and 6 joints of each foot, from 0 (normal) to 4 (complete loss of joint space, bony ankylosis, or luxation). The total JSN score ranges from 0 to 208 (worst).

Joints with gross osteolysis or pencil in cup were assigned the maximum score for both erosions and JSN.

The total mTSS score is the sum of the joint erosion and JSN scores and ranges from 0 (normal) to 528 (worst).

Change From Baseline in Modified Nail Psoriasis Severity Index (mNAPSI) Score at Week 24Baseline and Week 24

The investigator assessed each fingernail for onycholysis (separation of the nail plate from the nail bed) and oil-drop (salmon patch) dyschromia (reddish-brown discoloration under the nail plate) on a scale of 0 (none present) to 3 (\>30% of the nail), pitting (small, sharply defined depressions in the nail surface) on a scale of 0 (0 pits present) to 3 (\> 50 pits present), and nail plate crumbling on a scale of 0 (no crumbling) to 3 (\>50% of nail has crumbling) and presence (1) or absence (0) of leukonychia (white spots), splinter hemorrhages, nail bed hyperkeratosis, and red spots in the lunula.

The mNAPSI score is calculated as the sum of all the components for all of the participant's fingernails giving a range of possible scores from 0 (absence of nail psoriasis) to 130 (the most severe nail psoriasis). A negative change from Baseline indicates improvement.

Percentage of Participants With Resolution of Dactylitis at Week 24Week 24

Resolution of dactylitis is defined as a Leeds Dactylitis Index (LDI) score = 0.

LDI basic is a score based on finger circumference and tenderness, assessed across all digits. The LDI basic measures the ratio of the circumference of the affected digit to the circumference of the digit on the opposite hand or foot, using a minimum difference of 10% to define a dactylitic digit. The ratio of circumference is multiplied by a tenderness score (1 for tender, 0 for non-tender). If both sides of a digit are considered involved, or the circumference of the contralateral digit cannot be obtained, a standard reference table is used. Scores from each digit are summed to provide the final LDI. A higher LDI indicates worse dactylitis.

To increase sample size due to the smaller number of participants with dactylitis at Baseline, the pre-specified analysis of the resolution of dactylitis included pooled data from KEEPsAKE 1 (this study) and the companion study KEEPsAKE 2 (M15-998; NCT03671148).

Change From Baseline In Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) Score at Week 24Baseline and Week 24

The FACIT-Fatigue questionnaire is a self-administered patient questionnaire that consists of 13 questions designed to measure the degree of fatigue experienced by participants in the previous 7 days, including physical fatigue (e.g., I feel tired), functional fatigue (e.g., trouble finishing things), emotional fatigue (e.g., frustration), and social consequences of fatigue (e.g., limits social activity). Participants respond to the questions on a scale from 0 (not at all) to 4 (very much).

The FACIT-Fatigue score is computed by summing the item scores, after reversing those items that are worded in the negative direction. The FACIT-Fatigue score ranges from 0 to 52, where higher scores represent less fatigue.

A positive change from Baseline indicates improvement.

Percentage of Participants With an American College of Rheumatology 70% (ACR70) Response at Week 24Baseline and Week 24

Participants who met the following 3 conditions for improvement from Baseline were classified as meeting the ACR70 response criteria:

1. ≥ 70% improvement in 68-tender joint count;

2. ≥ 70% improvement in 66-swollen joint count; and

3. ≥ 70% improvement in at least 3 of the 5 following parameters:

* Physician global assessment of disease activity

* Patient global assessment of disease activity

* Patient assessment of pain

* Health Assessment Questionnaire - Disability Index (HAQ-DI)

* High-sensitivity C-reactive protein (hsCRP).

Trial Locations

Locations (256)

Duplicate_Azienda Ospedaliero-Universitaria Policlinico di Modena /ID# 207799

🇮🇹

Modena, Emilia-Romagna, Italy

Medvin Clinical Research /ID# 211127

🇺🇸

Whittier, California, United States

June DO, PC /ID# 208915

🇺🇸

Lansing, Michigan, United States

Joint & Muscle Research Instit /ID# 208620

🇺🇸

Charlotte, North Carolina, United States

Coastal Carolina Health Care /ID# 208619

🇺🇸

New Bern, North Carolina, United States

Paramount Medical Research Con /ID# 201583

🇺🇸

Middleburg Heights, Ohio, United States

Altoona Ctr Clinical Res /ID# 168037

🇺🇸

Duncansville, Pennsylvania, United States

Clinical Research Ctr Reading /ID# 168070

🇺🇸

Wyomissing, Pennsylvania, United States

Amarillo Ctr for Clin Research /ID# 208347

🇺🇸

Amarillo, Texas, United States

Precision Comprehensive Clinical Research Solutions /ID# 210597

🇺🇸

Fort Worth, Texas, United States

Kadlec Clinic Rheumatology /ID# 207969

🇺🇸

Kennewick, Washington, United States

Rheumatology and Pulmonary Clinic /ID# 200446

🇺🇸

Beckley, West Virginia, United States

Aurora Rheumatology and Immunotherapy Center /ID# 168066

🇺🇸

Franklin, Wisconsin, United States

Gundersen Clinic, Ltd /ID# 209459

🇺🇸

Onalaska, Wisconsin, United States

Framingham Centro Medico /ID# 210409

🇦🇷

La Plata, Buenos Aires, Argentina

Hospital General de Agudos J. M. Ramos Mejia /ID# 169164

🇦🇷

Buenos Aires, Ciuadad Autonoma De Buenos Aires, Argentina

Hospital Italiano de Buenos Aires /ID# 208474

🇦🇷

Ciudad Autonoma Buenos Aires, Ciuadad Autonoma De Buenos Aires, Argentina

Centro Medico Privado de Reumatologia /ID# 208343

🇦🇷

San Miguel de Tucuman, Tucuman, Argentina

Duplicate_Inst de Rehab Psicofisica /ID# 214681

🇦🇷

Buenos Aires, Argentina

Duplicate_Hospital Privado Univesitario /ID# 211623

🇦🇷

Cordoba, Argentina

The Canberra Hospital /ID# 207592

🇦🇺

Garran, Australian Capital Territory, Australia

Rheumatology Research Unit Sunshine Coast /ID# 207200

🇦🇺

Maroochydore, Queensland, Australia

Medical center Excelsior /ID# 167741

🇧🇬

Sofia, Bulgaria

Manitoba Clinic /ID# 206819

🇨🇦

Winnipeg, Manitoba, Canada

SKIN Centre for Dermatology /ID# 169604

🇨🇦

Peterborough, Ontario, Canada

K. Papp Clinical Research /ID# 169603

🇨🇦

Waterloo, Ontario, Canada

Groupe de Recherche en Maladies Osseuses Inc /ID# 169598

🇨🇦

Sainte-foy, Quebec, Canada

Duplicate_Policlinico Univ Tor Vergata /ID# 207271

🇮🇹

Rome, Italy

Centro Internacional de Estudios Clinicos /ID# 209908

🇨🇱

Santiago, Chile

Poliklinika Solmed /ID# 210965

🇭🇷

Zagreb, Grad Zagreb, Croatia

UHC Osijek /ID# 208623

🇭🇷

Osijek, Osjecko-baranjska Zupanija, Croatia

Klinicki bolnicki centar Split /ID# 208626

🇭🇷

Split, Splitsko-dalmatinska Zupanija, Croatia

Medical Center Kuna-Peric /ID# 208047

🇭🇷

Zagreb, Croatia

Poliklinika Bonifarm /ID# 208750

🇭🇷

Zagreb, Croatia

PV MEDICAL Services s.r.o. /ID# 210222

🇨🇿

Praha, Czechia

Revmacentrum MUDr. Mostera, s.r.o. /ID# 209025

🇨🇿

Brno, Czechia

Aarhus University Hospital /ID# 168761

🇩🇰

Aarhus C, Midtjylland, Denmark

Innomedica /ID# 211416

🇪🇪

Tallinn, Harjumaa, Estonia

MediTrials /ID# 207816

🇪🇪

Tartu, Tartumaa, Estonia

Turku University Hospital /ID# 207726

🇫🇮

Turku, Finland

Rheumazentrum Ruhrgebiet /ID# 207216

🇩🇪

Herne, Nordrhein-Westfalen, Germany

Immanuel Krankenhaus Berlin /ID# 207218

🇩🇪

Berlin-buch, Germany

MVZ Rheumatologie und Autoimmunmedizin Hamburg GmbH /ID# 209484

🇩🇪

Hamburg, Germany

424 General MILITARY Hospital /ID# 210974

🇬🇷

Efkarpia (Thessalonikis), Thessaloniki, Greece

Rambam Health Care Campus /ID# 208170

🇮🇱

Haifa, Israel

Barzilai Medical Center /ID# 207476

🇮🇱

Ashkelon, Israel

Meir Medical Center /ID# 207473

🇮🇱

Kfar Saba, Israel

Rabin Medical Center /ID# 207475

🇮🇱

Petakh Tikva, Israel

A.O.U. Policlinico G. Rodolico S.Marco - Presidio San Marco /ID# 207795

🇮🇹

Catania, Italy

Hanyang University Seoul Hospital /ID# 209263

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Duplicate_Konkuk University Medical Ctr /ID# 207509

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Kyungpook National Univ Hosp /ID# 207408

🇰🇷

Daegu, Korea, Republic of

Hospital Selayang /ID# 208938

🇲🇾

Batu Caves, Selangor, Malaysia

University Malaya Med Ctr /ID# 208937

🇲🇾

Kuala Lumpur, Malaysia

Malopolskie Centrum Kliniczne /ID# 208007

🇵🇱

Krakow, Malopolskie, Poland

Ulyanovsk Regional Clinical Hospital /ID# 169515

🇷🇺

Ulyanovsk, Russian Federation

Kazan State Medical University /ID# 169511

🇷🇺

Kazan, Tatarstan, Respublika, Russian Federation

Institute for Rheumatology /ID# 168199

🇷🇸

Belgrade, Beograd, Serbia

Hospital Universitario Torrecardenas /ID# 212716

🇪🇸

Almeria, Spain

Chung Shan Medical University Hospital /ID# 207257

🇨🇳

Taichung, Taiwan

Arthritis and Rheumatology /ID# 168046

🇺🇸

Atlanta, Georgia, United States

Precision Comprehensive Clinical Research Solutions /ID# 208386

🇺🇸

Colleyville, Texas, United States

Dallas VA Medical Center /ID# 208389

🇺🇸

Dallas, Texas, United States

Advanced Rheumatology of Houston /ID# 208354

🇺🇸

The Woodlands, Texas, United States

Royal Brisbane and Women's Hospital /ID# 212785

🇦🇺

Herston, Queensland, Australia

Percuro Clinical Research, Ltd /ID# 169601

🇨🇦

Victoria, British Columbia, Canada

DM Clinical Research /ID# 208351

🇺🇸

Tomball, Texas, United States

SER - Serviços Especializados em Reumatologia /ID# 207489

🇧🇷

Salvador, Bahia, Brazil

Special Hospital for Rheuma /ID# 210284

🇷🇸

Novi Sad, Vojvodina, Serbia

General Hospital Asklepieio Voulas /ID# 212956

🇬🇷

Athens, Attiki, Greece

Naval Hospital of Athens /ID# 206838

🇬🇷

Athens, Greece

LMK Sevicos Medicos S/S /ID# 207491

🇧🇷

Porto Alegre, Rio Grande Do Sul, Brazil

Klaipeda University Hospital /ID# 207329

🇱🇹

Klaipeda, Lithuania

Centro Integral en Reumatologia S.A de C.V /ID# 208346

🇲🇽

Guadalajara, Jalisco, Mexico

Logan Health Research /ID# 213707

🇺🇸

Kalispell, Montana, United States

Thermium s.r.o. /ID# 208015

🇸🇰

Piestany, Slovakia

Midlands Partnership NHS Foundation Trust /ID# 214941

🇬🇧

Stafford, Staffordshire, United Kingdom

Centro de Enfermedades del Hígado y Aparato Digestivo /ID# 169163

🇦🇷

Rosario, Santa Fe, Argentina

Dr. Latha Naik /ID# 212188

🇨🇦

Saskatoon, Saskatchewan, Canada

North Estonia Medical Centre /ID# 208325

🇪🇪

Mustamäe Linnaosa, Harjumaa, Estonia

Unidade Local de Saúde do Alto Minho, EPE - Hospital Conde de Bertiandos /ID# 208147

🇵🇹

Ponte de Lima, Viana Do Castelo, Portugal

Dr Jenny Potts /ID# 168691

🇿🇦

Port Elizabeth, Eastern Cape, South Africa

NHS Greater Glasgow and Clyde /ID# 214942

🇬🇧

Glasgow, Scotland, United Kingdom

Ite Pihlajanlinna Kuopio /ID# 208322

🇫🇮

Kuopio, Finland

VAKK Dr. Kilda's Clinic /ID# 207330

🇱🇹

Kaunas, Lithuania

Institute for Rheumatology /ID# 168198

🇷🇸

Belgrade, Beograd, Serbia

Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation /ID# 207567

🇨🇳

Chia-Yi, Taiwan

CTR Estudios Clinicos /ID# 208166

🇨🇱

Providencia, Chile

Changi General Hospital /ID# 208965

🇸🇬

Singapore, Singapore

Helsinki University Hospital /ID# 207724

🇫🇮

Helsinki, Uusimaa, Finland

Eukarya PharmaSite, SC /ID# 208431

🇲🇽

Monterrey, Nuevo Leon, Mexico

Spitalul Clinic de Recuperare Iasi /ID# 207371

🇷🇴

Iasi, Romania

Bispebjerg and Frederiksberg Hospital /ID# 207576

🇩🇰

Frederiksberg, Hovedstaden, Denmark

Affidea Praha s.r.o. /ID# 210223

🇨🇿

Praha, Czechia

MEDICAL PLUS, s.r.o. /ID# 210439

🇨🇿

Uherske Hradiste, Czechia

DOM Centro de Reumatologia /ID# 208479

🇦🇷

Ciudad Autonoma de Buenos Aire, Ciuadad Autonoma De Buenos Aires, Argentina

Rheumatology Center of San Diego /ID# 201642

🇺🇸

San Diego, California, United States

Medication Management, LLC /ID# 211734

🇺🇸

Greensboro, North Carolina, United States

Pinnacle Research Group /ID# 167955

🇺🇸

Anniston, Alabama, United States

Arizona Arthritis & Rheumatology Research, PLLC /ID# 209875

🇺🇸

Tucson, Arizona, United States

Inland Rheum Clin Trials Inc. /ID# 201641

🇺🇸

Upland, California, United States

Southern Arizona VA Health Care System /ID# 209247

🇺🇸

Tucson, Arizona, United States

Arthritis and Rheumatism Associates /ID# 209882

🇺🇸

Jonesboro, Arkansas, United States

Valerius Medical Group & Research Center /ID# 207428

🇺🇸

Los Alamitos, California, United States

New England Research Associates, LLC /ID# 207237

🇺🇸

Bridgeport, Connecticut, United States

Arthritis & Rheumatic Disease Specialties /ID# 210802

🇺🇸

Aventura, Florida, United States

Arthritis & Osteoporosis Center /ID# 207236

🇺🇸

Hamden, Connecticut, United States

Rheumatology Associates of South Florida (RASF) - Clinical Research /ID# 211099

🇺🇸

Boca Raton, Florida, United States

Sweet Hope Research Specialty Inc /ID# 209393

🇺🇸

Hialeah, Florida, United States

Jacksonville Center for Clinical Research /ID# 209876

🇺🇸

Jacksonville, Florida, United States

IRIS Research and Development, LLC /ID# 208955

🇺🇸

Plantation, Florida, United States

Springfield Clinic /ID# 200244

🇺🇸

Springfield, Illinois, United States

Clinical Pharmacology Study Gr /ID# 168019

🇺🇸

Worcester, Massachusetts, United States

Klein and Associates MD /ID# 169483

🇺🇸

Hagerstown, Maryland, United States

St. Paul Rheumatology /ID# 208471

🇺🇸

Eagan, Minnesota, United States

Center for Rheumatology LLP /ID# 207313

🇺🇸

Albany, New York, United States

NYU Langone Ambulatory Care Brooklyn Heights /ID# 207310

🇺🇸

Brooklyn, New York, United States

STAT Research, Inc. /ID# 213805

🇺🇸

Springboro, Ohio, United States

Velocity Clinical Research /ID# 200452

🇺🇸

Blue Ash, Ohio, United States

Marietta Memorial Hospital /ID# 210179

🇺🇸

Marietta, Ohio, United States

Allegheny Health Network Research Institute /ID# 210349

🇺🇸

Pittsburgh, Pennsylvania, United States

Holy Family Memorial, Inc. /ID# 209387

🇺🇸

Manitowoc, Wisconsin, United States

Fundacion CIDEA /ID# 210494

🇦🇷

Ciudad Autonoma de Buenos Aire, Ciuadad Autonoma De Buenos Aires, Argentina

Hospital Militar Central Cirujano Mayor Dr. Cosme Argerich /ID# 211622

🇦🇷

Ciudad Autonoma de Buenos Aire, Ciuadad Autonoma De Buenos Aires, Argentina

Instituto CAICI /ID# 169168

🇦🇷

Rosario, Santa Fe, Argentina

Cimer /Id# 169167

🇦🇷

San Miguel de Tucuman, Argentina

Griffith University /ID# 207505

🇦🇺

Southport, Queensland, Australia

ReumaClinic /ID# 208213

🇧🇪

Genk, Belgium

Flinders Medical Centre /ID# 210562

🇦🇺

Bedford, Park, South Australia, Australia

Duplicate_UZ Ghent /ID# 210036

🇧🇪

Ghent, Oost-Vlaanderen, Belgium

University Clinical Centre of the Republic of Srpska /ID# 208269

🇧🇦

Banja Luka, Republika Srpska, Bosnia and Herzegovina

University Clinical Centre of the Republic of Srpska /ID# 210047

🇧🇦

Banja Luka, Republika Srpska, Bosnia and Herzegovina

University Clinical Centre of the Republic of Srpska /ID# 208268

🇧🇦

Banja Luka, Republika Srpska, Bosnia and Herzegovina

ZNA - Jan Palfijn /ID# 208212

🇧🇪

Merksem, Belgium

Clinical Center University of Sarajevo /ID# 208272

🇧🇦

Sarajevo, Bosnia and Herzegovina

CMiP - Centro Mineiro de Pesquisa Ltda - ME /ID# 207496

🇧🇷

Juiz de Fora, Minas Gerais, Brazil

EDUMED Educacao em Saude S/S L /ID# 207488

🇧🇷

Curitiba, Parana, Brazil

CPCLIN - Centro de Pesquisas Clínicas /ID# 207493

🇧🇷

Sao Paulo, Brazil

Military Medical Academy Multiprofile Hospital /ID# 210829

🇧🇬

Sofia, Bulgaria

Medical center Medconsult /ID# 211399

🇧🇬

Pleven, Bulgaria

Diagnostic consultative center 17 Sofia /ID# 210506

🇧🇬

Sofia, Bulgaria

CIADS Research Co Ltd /ID# 169600

🇨🇦

Winnipeg, Manitoba, Canada

Poliklinika Repromed /ID# 208628

🇭🇷

Zagreb, Grad Zagreb, Croatia

Klinicki bolnicki centar Rijeka /ID# 208621

🇭🇷

Rijeka, Primorsko-goranska Zupanija, Croatia

Clinica Dermacross S.A /ID# 208163

🇨🇱

Vitacura Santiago, Chile

MUDr. Zuzana Stejfova - revmatologicka ambulance /ID# 209027

🇨🇿

Praha, Czechia

Center of Innovative Diagnostics and Therapeutics (CIRI GmbH) /ID# 209483

🇩🇪

Frankfurt, Germany

University General Hospital of Heraklion PA.G.N.I /ID# 206839

🇬🇷

Heraklion, Kriti, Greece

Advanced Rheumatology, PC /ID# 168042

🇺🇸

Lansing, Michigan, United States

Sheba Medical Center /ID# 207474

🇮🇱

Ramat Gan, Tel-Aviv, Israel

Olympion General Clinic SA /ID# 207048

🇬🇷

Patras, Greece

Azienda Ospedaliero Universitaria Ospedali Riuniti di Ancona /ID# 207269

🇮🇹

Ancona, Italy

Azienda Ospedaliera Universitaria di Verona/Ospedale Borgo Roma /ID# 207265

🇮🇹

Verona, Italy

M & M Centrs LTD /ID# 208733

🇱🇻

Adazi, Latvia

Riga East Clinical University Hospital /ID# 207223

🇱🇻

Riga, Latvia

D.Saulites-Kandevicas PP in Cardiology and Rheumatology /ID# 207224

🇱🇻

Liepaja, Latvia

Pauls Stradins Clinical University Hospital /ID# 207220

🇱🇻

Riga, Latvia

Clinic ORTO /ID# 216218

🇱🇻

Riga, Latvia

Hospital of Lithuanian University of Health Sciences Kaunas Clinics /ID# 207331

🇱🇹

Kaunas, Lithuania

Republican Siauliai hospital /ID# 207328

🇱🇹

Siauliai, Lithuania

Hospital Tuanku Jaafar /ID# 207919

🇲🇾

Seremban, Negeri Sembilan, Malaysia

Hospital Raja Permaisuri Bainun /ID# 207920

🇲🇾

Ipoh, Perak, Malaysia

CINTRE, Centro de Investigación y Tratamiento Reumatológico SC /ID# 208331

🇲🇽

Mexico City, Ciudad De Mexico, Mexico

Centro Peninsular de Investigación Clínica SCP /ID# 208345

🇲🇽

Colonia Centro, Yucatan, Mexico

Hospital General Regional No. 1 Dr. Carlos Mac Gregor Sánchez Navarro /ID# 210835

🇲🇽

Ciudad de Mexico, Mexico

RM Pharma Specialists S.A de C.V /ID# 208330

🇲🇽

Mexico City, Mexico

Antonius Ziekenhuis /ID# 208587

🇳🇱

Sneek, Fryslan, Netherlands

Waikato Hospital /ID# 213257

🇳🇿

Hamilton, Waikato, New Zealand

Universitair Medisch Centrum Groningen /ID# 208580

🇳🇱

Groningen, Netherlands

Medisch Centrum Leeuwarden /ID# 168453

🇳🇱

Leeuwarden, Netherlands

Middlemore Clinical Trials /ID# 213256

🇳🇿

Papatoetoe, Auckland, New Zealand

CGM Research Trust /ID# 210498

🇳🇿

Burwood, New Zealand

Spolka Lekarzy INTERCOR /ID# 210191

🇵🇱

Bydgoszcz, Kujawsko-pomorskie, Poland

Nasz Lekarz Przychodnie Medyczne /ID# 216176

🇵🇱

Torun, Kujawsko-pomorskie, Poland

Centrum Kliniczno-Badawcze /ID# 208010

🇵🇱

Elblag, Warminsko-mazurskie, Poland

Osteo-Medic S.C. /ID# 208008

🇵🇱

Bialystok, Podlaskie, Poland

Centrum Medyczne Reuma Park w Warszawie /ID# 210352

🇵🇱

Warsaw, Mazowieckie, Poland

ClinicMed Daniluk, Nowak Sp.j. /ID# 210824

🇵🇱

Bialystok, Podlaskie, Poland

McBk Sc /Id# 209132

🇵🇱

Grodzisk Mazowiecki, Mazowieckie, Poland

Centro Hospitalar de Vila Nova de Gaia/Espinho, EPE /ID# 208145

🇵🇹

Vila Nova De Gaia, Porto, Portugal

ETYKA-Osrodek Badan Klinicznych /ID# 216241

🇵🇱

Olsztyn, Warminsko-mazurskie, Poland

Centro Hospitalar do Baixo Vouga /ID# 215979

🇵🇹

Aveiro, Portugal

Instituto Português De Reumatologia /ID# 208149

🇵🇹

Lisboa, Portugal

CCA Braga - Hospital de Braga /ID# 208146

🇵🇹

Braga, Portugal

Mindful Medical Research /ID# 211129

🇵🇷

San Juan, Puerto Rico

Centro Hospitalar Universitário de Lisboa Norte, EPE - Hospital de Santa Maria /ID# 208148

🇵🇹

Lisboa, Portugal

Spitalul Clinic Sf. Maria /ID# 210054

🇷🇴

Bucuresti, Romania

Cabinet Medical Dr Triff Carina /Id# 207528

🇷🇴

Timisoara, Timis, Romania

Spitalul Clinic Judetean de Urgenta Cluj -Napoca /ID# 207340

🇷🇴

Cluj-Napoca, Romania

LLC Family Outpatient Clinic № /ID# 169510

🇷🇺

Korolev, Moskva, Russian Federation

LLC Medical Center /ID# 169516

🇷🇺

Novosibirsk, Novosibirskaya Oblast, Russian Federation

Federal Center for Brain and Neurotechnology /ID# 207646

🇷🇺

Moscow, Russian Federation

Nort-Western State Medical University n.a. Mechnikov /ID# 207641

🇷🇺

St. Petersburg, Sankt-Peterburg, Russian Federation

Institute for Rheumatology /ID# 168197

🇷🇸

Belgrade, Beograd, Serbia

Perm Regional Clinical Hospital /ID# 207642

🇷🇺

Perm, Russian Federation

Institute for Rheumatology /ID# 168194

🇷🇸

Belgrade, Beograd, Serbia

Military Medical Academy /ID# 168218

🇷🇸

Belgrade, Beograd, Serbia

Singapore General Hospital /ID# 207917

🇸🇬

Singapore, Singapore

Special Hospital for Rheuma /ID# 168255

🇷🇸

Novi Sad, Vojvodina, Serbia

National University Hospital /ID# 208599

🇸🇬

Singapore, Singapore

REUMA-GLOBAL, s.r.o. /ID# 208017

🇸🇰

Biely Kostol, Slovakia

MEDMAN s.r.o. /ID# 208018

🇸🇰

Martin, Slovakia

Reum.hapi s.r.o. /ID# 208016

🇸🇰

Nove Mesto nad Vahom, Slovakia

REUMAMED POPRAD s.r.o. /ID# 208407

🇸🇰

Poprad, Slovakia

University of Pretoria /ID# 167621

🇿🇦

Pretoria, Gauteng, South Africa

Dr Elsa van Duuren /ID# 207577

🇿🇦

Pretoria, Gauteng, South Africa

Arthritis Clinical Research Trials /ID# 167625

🇿🇦

Cape Town, Western Cape, South Africa

Consorci Corporacio Sanitaria Parc Tauli Sabadell /ID# 207830

🇪🇸

Sabadell, Barcelona, Spain

Hospital Universitario A Coruna - CHUAC /ID# 207826

🇪🇸

A Coruna, Spain

Synexus Helderberg Clinical Research Centre /ID# 210891

🇿🇦

Somerset West, Western Cape, South Africa

Orebro Universitetssjukhuset /ID# 207948

🇸🇪

Orebro, Orebro Lan, Sweden

Skane University hospital /ID# 210070

🇸🇪

Malmo, Skane Lan, Sweden

Hospital Universitario y Politecnico La Fe /ID# 207831

🇪🇸

Valencia, Spain

Winelands Medical Research Centre /ID# 167629

🇿🇦

Stellenbosch, Western Cape, South Africa

Hospital Universitario Germans Trias i Pujol /ID# 208543

🇪🇸

Badalona, Barcelona, Spain

Duplicate_Karolinska Univ Sjukhuset /ID# 208175

🇸🇪

Solna, Sweden

Falu Lasarett /ID# 210322

🇸🇪

Falun, Sweden

Hospital Parc de Salut del Mar /ID# 209698

🇪🇸

Barcelona, Spain

Linkou Chang Gung Memorial Ho /ID# 207255

🇨🇳

Taoyuan City, Taiwan

Duplicate_Vastmanlands Sjukhus /ID# 207943

🇸🇪

Vasteras, Sweden

Uppsala University Hospital /ID# 207944

🇸🇪

Uppsala, Sweden

MNPE Chernihiv Regional Hospital of the Chernihiv Region Council /ID# 207730

🇺🇦

Chernihiv, Ukraine

State Institution L. T. Malaya Therapy National Institution of NAMS of Ukraine /ID# 209556

🇺🇦

Kharkiv, Kharkivska Oblast, Ukraine

PNE City Multifunctional Hospital No.18 /ID# 207911

🇺🇦

Kharkiv, Ukraine

Communal Enterprise Volyn Regional Clinical hospital of the Volyn Regional Coun /ID# 208276

🇺🇦

Lutsk, Ukraine

PI "Poltava Regional Clinical Hospital n.a. M.V.Sklifosovsky" /ID# 207872

🇺🇦

Poltava, Ukraine

Medical Center OK Clinic /ID# 207749

🇺🇦

Kyiv, Ukraine

Lviv Municipal City Clinical Hospital #4 /ID# 207715

🇺🇦

Lviv, Ukraine

Duplicate_Barts Health NHS Trust /ID# 210534

🇬🇧

London, London, City Of, United Kingdom

Manchester University NHS Foundation Trust /ID# 207928

🇬🇧

Manchester, United Kingdom

Duplicate_Wirral University Teaching Hospital NHS Foundation Trust /ID# 210535

🇬🇧

Wirral, United Kingdom

Torbay and South Devon Nhs Foundation Trust /Id# 207931

🇬🇧

Torquay, United Kingdom

Affinity Clinical Research /ID# 210816

🇺🇸

Oak Brook, Illinois, United States

OrthoIllinois /ID# 205300

🇺🇸

Rockford, Illinois, United States

ForCare Clinical Research /ID# 168034

🇺🇸

Tampa, Florida, United States

Nashville Arthritis and Rheumatology /ID# 168069

🇺🇸

Nashville, Tennessee, United States

Health Research of Oklahoma /ID# 168027

🇺🇸

Oklahoma City, Oklahoma, United States

Physician Research Collaboration, LLC /ID# 208670

🇺🇸

Lincoln, Nebraska, United States

Hospital Clinico Universitario San Carlos /ID# 207832

🇪🇸

Madrid, Spain

Emeritus Research /ID# 207202

🇦🇺

Camberwell, Victoria, Australia

AZ Arthritis and Rheumotology Research, PLLC /ID# 209873

🇺🇸

Phoenix, Arizona, United States

Sun Valley Arthritis Center Ltd. /ID# 200270

🇺🇸

Peoria, Arizona, United States

Danbury Clinical Research, LLC /ID# 209517

🇺🇸

Danbury, Connecticut, United States

Monash Medical Centre /ID# 208034

🇦🇺

Clayton, Victoria, Australia

Research Institute of Rheumatology named after V.A. Nasonova /ID# 207643

🇷🇺

Moscow, Moskva, Russian Federation

Hospital Universitario 12 de Octubre /ID# 207827

🇪🇸

Madrid, Spain

Portsmouth Hospitals University NHS Trust /ID# 207932

🇬🇧

Portsmouth, United Kingdom

CNE Cherkasy Regional Hospital of Cherkasy Regional Council /ID# 207912

🇺🇦

Cherkasy, Ukraine

Khmelnytskyi Regional Hospital /ID# 207753

🇺🇦

Khmelnytskyi, Ukraine

Public Institution 6th City Clinical Hospital /ID# 207754

🇺🇦

Zaporizhzhia, Ukraine

MI Kryvyi Rih City Clinical Hospital No.2 /ID# 207748

🇺🇦

Kryvyi Rih, Ukraine

SIMED Health, LLC /ID# 207461

🇺🇸

Gainesville, Florida, United States

Rheum Assoc of Central FL /ID# 201622

🇺🇸

Orlando, Florida, United States

HMD Research LLC /ID# 208427

🇺🇸

Orlando, Florida, United States

Scientific Research Institute of Invalid Rehabilitation /ID# 207873

🇺🇦

Vinnytsia, Vinnytska Oblast, Ukraine

The Center for Rheumatology and Bone Research /ID# 168017

🇺🇸

Wheaton, Maryland, United States

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