MedPath

A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib in Adult and Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-TNF Therapy

Phase 3
Recruiting
Conditions
Hidradenitis Suppurativa
Interventions
Drug: Placebo
Drug: Upadacitinib
Registration Number
NCT05889182
Lead Sponsor
AbbVie
Brief Summary

Hidradenitis suppurativa (HS) is an inflammatory skin disease that causes painful lesions in the axilla (underarm), inguinal (groin) and anogenital (anal/genital) regions. This study will assess how safe and effective upadacitinib is in treating adult and adolescent participants with moderate to severe HS who have failed to respond to or are intolerant of anti-tumor necrosis factor (TNF) therapy. Adverse events and change in disease activity will be assessed.

Upadacitinib is an approved drug for ulcerative colitis, atopic dermatitis, rheumatoid arthritis, psoriatic arthritis, and axial spondylarthritis and is being developed for the treatment of HS. This study is "double-blinded", meaning that neither the trial participants nor the study doctors will know who will be given upadacitinib and who will be given placebo. This study is comprised of 3 periods. In Period 1, participants are randomized into 2 groups called treatment arms where each group receives a different treatment. There is a 1 in 2 chance that participants will be assigned to placebo. In Period 2, participants are placed into 6 different groups depending on their placement and results in Period 1. Period 3 is the long-term extension period where participants will continue treatment from Period 2. Approximately 1328 adult and adolescent participants diagnosed with HS will be enrolled in approximately 275 sites worldwide.

Participants will receive oral tablets of upadacitinib or placebo once daily for 36 weeks in Period 1 and Period 2. Eligible participants from Period 1 and Period 2 will enter Period 3 and receive oral tablets of upadacitinib or placebo once daily for 68 weeks. Participants will be followed up for approximately 30 days.

There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular outpatient visits during the study. The effect of the treatment will be checked by medical assessments, checking for side effects and completing questionnaires.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1328
Inclusion Criteria
  • Diagnosis of HS for at least 6 months prior to Baseline, as determined by the investigator (i.e., through medical history and interview of subject).
  • Documented history of previous use of ≥ 1 TNF inhibitor for HS for at least 12 weeks and/or 1 approved non-anti-TNF biologic therapy for HS for at least 16 weeks characterized by inadequate response or for any duration characterized by intolerance as determined by the investigator.
  • Participant must have a total AN count of ≥ 5 at Baseline.
  • HS lesions must be present in at least 2 distinct anatomic areas at Baseline.
  • At least 1 anatomic area of HS involvement characterized as Hurley Stage II or higher at Baseline.
  • Draining fistula count of ≤ 20 at Baseline.
Read More
Exclusion Criteria
  • History of active skin disease other than HS that could interfere with the assessment of HS, including skin infections (bacterial, fungal, or viral) requiring systemic treatment within 4 weeks of the Baseline visit.
  • Treatment with any investigational drug of chemical or biologic nature within a minimum of 30 days or 5 half-lives (whichever is longer) prior to the first dose of study drug or be currently enrolled in another interventional clinical study. Investigational drugs are also prohibited during the study.
  • Previous treatment with any cell-depleting therapies including but not limited to anti-CD20 (e.g., rituximab) within 12 months prior to Baseline or until B cell count returns to normal level or pre-treatment level.
  • Use of prescription topical therapies (including topical antibiotics) that can also be used to treat HS within 14 days prior to the Baseline visit.
  • Received any systemic (including oral) antibiotic treatment for HS or any other chronic inflammatory disorder within 14 days prior to the Baseline visit.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Period 2: Group 2 - PlaceboPlaceboParticipants who were randomized to placebo in Period 1 who achieve HiSCR 50 (clinical responder, CR) at Week 16 will continue to receive placebo once daily for 20 weeks.
Period 2: Group 3 - Upadacitinib Dose AUpadacitinibParticipants who were randomized to upadacitinib Dose A in Period 1 who did not achieve HiSCR 50 (CNR) at Week 16 will continue to receive upadacitinib Dose A once daily for 20 weeks.
Period 2: Group 6 - PlaceboPlaceboParticipants who were randomized to upadacitinib Dose A in Period 1 who achieve HiSCR 50 (CR) at Week 16 will receive placebo once daily for 20 weeks.
Period 1: PlaceboPlaceboParticipants will receive Placebo once daily for 16 weeks.
Period 2: Group 1 - Upadacitinib Dose AUpadacitinibParticipants who were randomized to placebo in Period 1 who did not achieve HiSCR 50 (clinical non-responder, CNR) at Week 16 will receive Upadacitinib Dose A once daily for 20 weeks.
Period 2: Group 4 - Upadacitinib Dose AUpadacitinibParticipants who were randomized to upadacitinib Dose A in Period 1 who achieve HiSCR 50 (CR) at Week 16 will receive upadacitinib Dose A once daily for 20 weeks.
Period 3: Long-Term ExtensionPlaceboEligible participants will continue to receive upadacitinib or placebo for 68 weeks. Participants will be followed-up for approximately 30 days.
Period 3: Long-Term ExtensionUpadacitinibEligible participants will continue to receive upadacitinib or placebo for 68 weeks. Participants will be followed-up for approximately 30 days.
Period 2: Group 5 - Upadacitinib Dose BUpadacitinibParticipants who were randomized to upadacitinib Dose A in Period 1 who achieve HiSCR 50 (CR) at Week 16 will receive upadacitinib Dose B once daily for 20 weeks.
Period 1: Upadacitinib Dose AUpadacitinibParticipants will receive Upadicitinib Dose A once daily for 16 weeks.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants Achieving Hidradenitis Suppurative Clinical Response (HiSCR) 50Baseline to Week 16

HiSCR 50 is defined as at least a 50% reduction in the total abscess and inflammatory nodule (AN) count with no increase in abscess count and no increase in draining fistula count relative to Baseline.

Secondary Outcome Measures
NameTimeMethod
Percentage of Participants Achieving Numeric Rating Scale 30 (NRS30) at Week 4 Among Participants with NRS ≥ 3 at BaselineBaseline to Week 4

Achievement will be considered at least a 30% reduction and at least 2 units reduction from Baseline in the Participant's Global Assessment (PGA) of HS-related skin pain NRS based on worst skin pain in a 24-hour recall period (maximal daily pain). The PGA Skin Pain is an 11-point numerical rating scale with ratings for the item ranging from 0 (no skin pain) to 10 (skin pain as bad as you can imagine).

Occurrence of Hidradenitis Suppurativa (HS) Flare During Period 1Week 16

Defined as at least one occurrence of a ≥ 25% increase in AN count, with a minimum absolute increase of 2 relative to Baseline.

Change from Baseline in Hidradenitis Suppurativa Symptom Assessment (HSSA)Baseline to Week 16

The HSSA (24-hour recall) is a 9-item PRO questionnaire developed to assess the primary symptoms of HS in the 7 consecutive days prior to assessments. Each item of the HSSA is scored on an 11-point (0 to 10) NRS, where 0 represents no symptoms and 10 represents extreme symptom experience.

Change from Baseline in Hidradenitis Suppurativa Impact Assessment (HSIA)Baseline to Week 16

The HSIA is an 18-item PRO questionnaire developed to assess the impact of HS on the daily lives of subjects in the 7 days prior to the assessment. Items 1 - 16 of the HSIA are scored on a 0 to 10 NRS, where 0 represents no impact and 10 represents extreme impact.

Percentage of Participants Achieving Hidradenitis Suppurative Clinical Response (HiSCR) 75Baseline to Week 16

HiSCR 75 is defined as at least a 75% reduction in the total abscess and inflammatory nodule (AN) count with no increase in abscess count and no increase in draining fistula count relative to Baseline.

Change from Baseline in Dermatology Life Quality Index (DLQI) for Adult Participants and Adolescent Participants Age ≥16 Years OldBaseline to Week 16

The DLQI and the CDLQI are both 10-item questionnaires used to assess the impact of hidradenitis suppurativa (HS) disease symptoms and treatment on quality of life that consists of 10 questions scored on a 4-point scale where 0 = not at all/not relevant; 1 = a little; 2 = a lot; and 3 = very much.

Change from Baseline in Hidradenitis Suppurativa (HS)-Related Odor, Based on Hidradenitis Suppurativa Symptom Assessment (HSSA) Question 8Baseline to Week 16

The HSSA (24-hour recall) is a 9-item PRO questionnaire developed to assess the primary symptoms of HS in the 7 consecutive days prior to assessments. Each item of the HSSA is scored on an 11-point (0 to 10) NRS, where 0 represents no symptoms and 10 represents extreme symptom experience.

Change from Baseline in the Patient's Global Assessment of Hidradenitis Suppurativa (HS)-Related Skin Pain NRSAt Week 8

The PGA Skin Pain is an 11-point numerical rating scale with ratings for the item ranging from 0 (no skin pain) to 10 (skin pain as bad as you can imagine) that is used to assess the worst pain due to HS. Patients are asked to respond to the item based on a recall period of "the last 24 hours

Trial Locations

Locations (246)

Cahaba Dermatology & Skin Health Center /ID# 254876

🇺🇸

Birmingham, Alabama, United States

Medical Dermatology Specialists /ID# 254226

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Phoenix, Arizona, United States

Mayo Clinic - Scottsdale /ID# 254388

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Scottsdale, Arizona, United States

Banner University Medicine Dermatology /ID# 255853

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Tucson, Arizona, United States

Clinical Trials Institute - Northwest Arkansas /ID# 254924

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Fayetteville, Arkansas, United States

Burke Pharmaceutical Research /ID# 254238

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Hot Springs, Arkansas, United States

Arkansas Research Trials /ID# 254233

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North Little Rock, Arkansas, United States

NW Arkansas Clinical Trials Center /ID# 254311

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Rogers, Arkansas, United States

Joseph Raoof Md,Inc /Id# 254374

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Encino, California, United States

Dermatology Research Associates /ID# 254846

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Los Angeles, California, United States

Integrative Skin Science and Research /ID# 254930

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Sacramento, California, United States

University of California Davis Health /ID# 254229

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Sacramento, California, United States

Medderm Associates /ID# 253800

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San Diego, California, United States

Clinical Trials Research Institute /ID# 254466

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Thousand Oaks, California, United States

UConn Health Main /ID# 254507

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Farmington, Connecticut, United States

Yale University School of Medicine /ID# 254586

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New Haven, Connecticut, United States

Skin Care Research Boca Raton /ID# 253814

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Boca Raton, Florida, United States

Apex Clinical Trials /ID# 255756

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Brandon, Florida, United States

Florida Academic Dermatology Center /ID# 254011

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Coral Gables, Florida, United States

Skin Care Research - Hollywood /ID# 254508

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Hollywood, Florida, United States

Life Clinical Trials /ID# 258613

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Margate, Florida, United States

Skin Care Research - Tampa /ID# 256440

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Tampa, Florida, United States

Advanced Clinical Research Institute /ID# 253746

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Tampa, Florida, United States

Avita Clinical Research /ID# 254471

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Tampa, Florida, United States

Centricity Research /ID# 255470

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Columbus, Georgia, United States

Treasure Valley Medical Research /ID# 255208

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Boise, Idaho, United States

Northwestern University Feinberg School of Medicine /ID# 254503

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Chicago, Illinois, United States

DeNova Research /ID# 254372

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Chicago, Illinois, United States

NorthShore University HealthSystem - Skokie /ID# 254389

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Skokie, Illinois, United States

Dawes Fretzin, LLC /ID# 254390

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Indianapolis, Indiana, United States

Options Research Group /ID# 254537

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West Lafayette, Indiana, United States

U.S. Dermatology Partners Leawood /ID# 255838

🇺🇸

Leawood, Kansas, United States

Massachusetts General Hospital /ID# 261093

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Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center /ID# 253811

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Boston, Massachusetts, United States

Beacon Clinical Research, LLC /ID# 254419

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Quincy, Massachusetts, United States

UMass Memorial Medical Center /ID# 258839

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Worcester, Massachusetts, United States

Michigan Dermatology Institute /ID# 254468

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Waterford, Michigan, United States

Dermatology and Skin Center of Lees Summit /ID# 257546

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Lee's Summit, Missouri, United States

MediSearch Clinical Trials /ID# 254392

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Saint Joseph, Missouri, United States

SSM Health Saint Louis University Hospital /ID# 256437

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Saint Louis, Missouri, United States

Washington University School of Medicine - St. Louis /ID# 254506

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Saint Louis, Missouri, United States

Vivida Dermatology- Flamingo /ID# 254227

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Las Vegas, Nevada, United States

Skin Cancer and Dermatology Institute - Reno /ID# 254410

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Reno, Nevada, United States

NorthWell Health - Dermatology /ID# 254704

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New Hyde Park, New York, United States

Schweiger Dermatology, P.C. /ID# 254232

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New York, New York, United States

Onsite Clinical Solutions /ID# 254854

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Charlotte, North Carolina, United States

Duke University (School of Medicine) /ID# 256898

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Durham, North Carolina, United States

ClinOhio Research Services /ID# 254851

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Columbus, Ohio, United States

Dermatologists of Southwest Ohio, Inc /ID# 254297

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Mason, Ohio, United States

Lynn Institute of Oklahoma City /ID# 253791

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Oklahoma City, Oklahoma, United States

Oregon Health and Science University /ID# 254929

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Portland, Oregon, United States

Penn State Milton S. Hershey Medical Center /ID# 254925

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Hershey, Pennsylvania, United States

Paddington Testing Co., Inc. /ID# 254394

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Philadelphia, Pennsylvania, United States

Clinical Research of Philadelphia, LLC /ID# 255308

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Philadelphia, Pennsylvania, United States

Dermatology Associates of Knoxville /ID# 261082

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Knoxville, Tennessee, United States

Arlington Research Center, Inc /ID# 253805

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Arlington, Texas, United States

Bellaire Dermatology Associates /ID# 253797

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Bellaire, Texas, United States

Dermatology Treatment and Research Center /ID# 253795

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Dallas, Texas, United States

Modern Research Associates, PLLC /ID# 253810

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Dallas, Texas, United States

HRMD Research Dallas /ID# 255256

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Dallas, Texas, United States

Dallas Fort Worth Clinical Research Associates (DFWCRA) /ID# 256438

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Grapevine, Texas, United States

Suzanne Bruce and Associates-Houston /ID# 254228

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Houston, Texas, United States

Texas Dermatology Research Center, LLC /ID# 254928

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Plano, Texas, United States

Center for Clinical Studies Webster TX /ID# 254242

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Webster, Texas, United States

University of Utah /ID# 254452

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Murray, Utah, United States

University of Virginia - Dermatology /ID# 254535

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Charlottesville, Virginia, United States

The Education & Research Foundation, Inc. /ID# 254852

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Lynchburg, Virginia, United States

Virginia Clinical Research /ID# 254538

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Norfolk, Virginia, United States

North Sound Dermatology /ID# 254554

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Mill Creek, Washington, United States

Premier Clinical Research /ID# 254847

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Spokane, Washington, United States

Buenos Aires Skin /ID# 255299

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

Instituto de Neumonologia y Dermatologia /ID# 254903

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

Psoriahue Med Interdisciplinar /ID# 257202

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

Consultorios Reumatologicos Pampa /ID# 255555

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

Centro de Investigacion y Prevencion Cardiovascular (CIPREC) /ID# 255474

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Buenos Aires, Argentina

Hospital Italiano /ID# 254905

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Caba, Argentina

Paratus Clinical Research Woden /ID# 254670

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Phillip, Australian Capital Territory, Australia

Momentum Clinical Research /ID# 254411

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Darlinghurst, New South Wales, Australia

Skin Health Institute Inc /ID# 254416

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Carlton, Victoria, Australia

Sinclair Dermatology - Melbourne /ID# 254412

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East Melbourne, Victoria, Australia

The Alfred Hospital /ID# 254414

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Melbourne, Victoria, Australia

Ordensklinikum Linz GmbH Elisabethinen /ID# 253458

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Linz, Oberoesterreich, Austria

Medizinische Universitaet Graz /ID# 253448

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Graz, Steiermark, Austria

Medizinische Universitaet Wien /ID# 254096

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Vienna, Wien, Austria

Universite Libre de Bruxelles - Hopital Erasme /ID# 254082

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Anderlecht, Bruxelles-Capitale, Belgium

Universitair Ziekenhuis Brussel /ID# 254223

🇧🇪

Jette, Bruxelles-Capitale, Belgium

Cliniques Universitaires UCL Saint-Luc /ID# 254087

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Woluwe-Saint-Lambert, Bruxelles-Capitale, Belgium

Grand Hôpital De Charleroi - Notre Dame /ID# 254091

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Charleroi, Hainaut, Belgium

CHU de Liège /ID# 254085

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Liège, Liege, Belgium

UZ Gent /ID# 254090

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Gent, Oost-Vlaanderen, Belgium

Universitair Ziekenhuis Leuven /ID# 254089

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Leuven, Vlaams-Brabant, Belgium

Instituto de Pesquisa e Ensino CLIGEDIMUNO - IPEC /ID# 254369

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Macaé, Rio De Janeiro, Brazil

Hospital Moinhos de Vento /ID# 254366

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Porto Alegre, Rio Grande Do Sul, Brazil

Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto /ID# 254367

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Ribeirão Preto, Sao Paulo, Brazil

Centro de Desenvolvimento em Estudos Clinicos Brasil - CDEC /ID# 254368

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São Paulo, Sao Paulo, Brazil

Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao /ID# 254370

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Sao Paulo, Brazil

Acibadem City Clinic Tokuda University Hospital EAD /ID# 253331

🇧🇬

Sofia, Bulgaria

Ambulatory for Specialized Medical Care for skin and venereal diseases /ID# 253329

🇧🇬

Sofia, Bulgaria

Diagnostic consultative center Focus-5 /ID# 253327

🇧🇬

Sofiya, Bulgaria

UMHAT Professor Stoyan Kirkovich /ID# 253328

🇧🇬

Stara Zagora, Bulgaria

Dermatology Research Institute - Blackfoot Trail /ID# 261413

🇨🇦

Calgary, Alberta, Canada

Beacon Dermatology Inc /ID# 254564

🇨🇦

Calgary, Alberta, Canada

Rejuvenation Dermatology - Edmonton Downtown /ID# 254715

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Edmonton, Alberta, Canada

Dr. Chih-ho Hong Medical Inc. /ID# 254378

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Surrey, British Columbia, Canada

Enverus Medical Research /ID# 254380

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Surrey, British Columbia, Canada

Wiseman Dermatology Research /ID# 254117

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Winnipeg, Manitoba, Canada

Karma Clinical Trials /ID# 254120

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St. John's, Newfoundland and Labrador, Canada

LEADER Research /ID# 254379

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Hamilton, Ontario, Canada

DermEffects /ID# 254116

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London, Ontario, Canada

Lynde Institute for Dermatology /ID# 254713

🇨🇦

Markham, Ontario, Canada

Dr. S.K. Siddha Medicine Professional Corporation /ID# 254714

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Newmarket, Ontario, Canada

York Dermatology Clinic and Research Centre /ID# 254115

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Richmond Hill, Ontario, Canada

Research Toronto /ID# 255273

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Toronto, Ontario, Canada

CHU Sainte-Justine /ID# 254118

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Montreal, Quebec, Canada

Diex Recherche Québec Inc. /ID# 254381

🇨🇦

Québec, Quebec, Canada

Dre Angelique Gagne-Henley M.D. inc. /ID# 255632

🇨🇦

Saint-Jerome, Quebec, Canada

SkinSense Dermatology /ID# 254119

🇨🇦

Saskatoon, Saskatchewan, Canada

Fundacion Innovacion Cardiovascular /ID# 254561

🇨🇱

Independencia, Region Metropolitana De Santiago, Chile

Centro Medico Skin Med SPA /ID# 254560

🇨🇱

Las Condes, Region Metropolitana Santiago, Chile

Centro Internacional de Estudios Clinicos - CIEC /ID# 254559

🇨🇱

Santiago, Region Metropolitana Santiago, Chile

Clinica Dermacross /ID# 254558

🇨🇱

Vitacura, Region Metropolitana Santiago, Chile

Clinisalud del sur /ID# 254797

🇨🇴

Medellin, Antioquia, Colombia

Centro Integral de Reumatología del Caribe SAS - Circaribe SAS /ID# 255278

🇨🇴

Barranquilla, Atlantico, Colombia

Centro de Investigacion en Reumatologia y especialidades Medicas S.A.S- CIREEM /ID# 254796

🇨🇴

Bogotá, Cundinamarca, Colombia

DermaPlus - Poliklinika za dermatologiju i venerologiju /ID# 253587

🇭🇷

Zagreb, Grad Zagreb, Croatia

Klinicki bolnicki centar Zagreb /ID# 253786

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Zagreb, Grad Zagreb, Croatia

Klinika za dječje bolesti Zagreb /ID# 253588

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Zagreb, Grad Zagreb, Croatia

Poliklinika Solmed /ID# 254732

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Zagreb, Grad Zagreb, Croatia

Klinicki Bolnicki Centar (KBC) Split /ID# 253789

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Split, Splitsko-dalmatinska Zupanija, Croatia

Naftalan - Specijalna bolnica za medicinsku rehabilitaciju /ID# 253586

🇭🇷

Ivanic-Grad, Zagrebacka Zupanija, Croatia

Specialty hospital Medico /ID# 254731

🇭🇷

Rijeka, Croatia

Karlovarska Krajska Nemocnice - Karlovy Vary /ID# 253456

🇨🇿

Karlovy Vary, Czechia

Duplicate_Fakultni Nemocnice v Motole /ID# 253455

🇨🇿

Prague, Czechia

Fakultni nemocnice Kralovske Vinohrady /ID# 253454

🇨🇿

Praha, Czechia

Terveystalo Tampere /ID# 253968

🇫🇮

Tampere, Pirkanmaa, Finland

Oulun yliopistollinen sairaala /ID# 253969

🇫🇮

Oulu, Pohjois-Pohjanmaa, Finland

Chu de Nice-Hopital Larchet Ii /Id# 253504

🇫🇷

Nice, Alpes-Maritimes, France

Centre Hospitalier Universitaire de Bordeaux - Groupe Hospitalier Saint-Andre /ID# 254139

🇫🇷

Bordeaux, Gironde, France

CHU de Nantes, Hotel Dieu -HME /ID# 254114

🇫🇷

Nantes, Pays-de-la-Loire, France

Hopital Prive d'Antony /ID# 253501

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Antony, Ile-de-France, France

Polyclinique Courlancy /ID# 254680

🇫🇷

Reims, Marne, France

HCL - Hopital Edouard Herriot /ID# 253500

🇫🇷

Lyon, Rhone, France

Magdeburger Company for Medical Studies & Services GmbH /ID# 255151

🇩🇪

Magdeburg, Germany

Klinikum Ruhr Univ Bochum /ID# 253690

🇩🇪

Bochum, Germany

Universitaetsklinikum Regensburg /ID# 253692

🇩🇪

Regensburg, Germany

Studienzentrum an der Hase GbR Dr. Weyergraf/Dr. Frick/Thomas Heiber /ID# 254510

🇩🇪

Bramsche, Niedersachsen, Germany

Havelklinik /ID# 254194

🇩🇪

Berlin, Germany

Dermatologie Quist-BAG Dres. med. Quist PartG /ID# 253691

🇩🇪

Mainz, Germany

Klinik am Biederstein /ID# 254195

🇩🇪

Munich, Germany

401 GSNA - 401 Army General Hospital /ID# 253499

🇬🇷

Athens, Attiki, Greece

University General Hospital Attikon /ID# 253495

🇬🇷

Athens, Attiki, Greece

General Hospital Andreas Syggros /ID# 253498

🇬🇷

Athens, Attiki, Greece

Papageorgiou General Hospital /ID# 253496

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Thessaloniki, Greece

Somogy Varmegyei Kaposi Mor Oktato Korhaz /ID# 253913

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Kaposvár, Somogy, Hungary

Szegedi Tudományegyetem /ID# 255142

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Szeged, Hungary

Hospital of Skin and Venereal Diseases- Thessaloniki /ID# 253497

🇬🇷

Thessaloniki, Greece

Pecsi Tudomanyegyetem Klinikai Kozpont /ID# 253753

🇭🇺

Pecs, Baranya, Hungary

St James Hospital /ID# 253973

🇮🇪

Dublin 8, Dublin, Ireland

South Infirmary Victoria University Hospital /ID# 253975

🇮🇪

Cork, Ireland

Debreceni Egyetem-Klinikai Kozpont /ID# 253637

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Debrecen, Hajdu-Bihar, Hungary

Vas Varmegyei Markusovszky Egyetemi Oktatokorhaz /ID# 254377

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Szombathely, Vas, Hungary

Csalogany Orvosi Kozpont /ID# 255063

🇭🇺

Budapest, Hungary

Duplicate_Obudai Egeszsegugyi Centrum Kft. /ID# 256366

🇭🇺

Budapest, Hungary

University Hospital Galway /ID# 253976

🇮🇪

Galway, Ireland

DERMA-B Egeszsegugyi es Szolgaltato - Debrecen - Gyepusor Utca /ID# 253638

🇭🇺

Debrecen, Hungary

University College Dublin /ID# 253971

🇮🇪

Dublin, Ireland

Waterford Regional Hospital /ID# 254038

🇮🇪

Waterford, Ireland

Rambam Health Care Campus /ID# 254406

🇮🇱

Haifa, H_efa, Israel

ZIV Medical Center /ID# 254403

🇮🇱

Safed, HaTsafon, Israel

Sheba Medical Center /ID# 254545

🇮🇱

Ramat Gan, Tel-Aviv, Israel

Tel Aviv Sourasky Medical Center /ID# 254404

🇮🇱

Tel Aviv, Tel-Aviv, Israel

Rabin Medical Center /ID# 254405

🇮🇱

Haifa, Israel

Azienda Ospedaliero-Universitaria di Ferrara - Arcispedale S.Anna /ID# 254496

🇮🇹

Cona, Ferrara, Italy

AZIENDA USL TOSCANA CENTRO - Ospedale Piero Palagi /ID# 254495

🇮🇹

Florence, Firenze, Italy

Azienda Ospedaliera Universitaria Policlinico Tor Vergata /ID# 254498

🇮🇹

Rome, Roma, Italy

Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Università Cattolica /ID# 254500

🇮🇹

Rome, Roma, Italy

ASST degli Spedali Civili di Brescia /ID# 254875

🇮🇹

Brescia, Italy

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico /ID# 254502

🇮🇹

Milano, Italy

Azienda Ospedaliero-Universitaria di Modena /ID# 254874

🇮🇹

Modena, Italy

Azienda Ospedaliero Universitaria Pisana /ID# 254501

🇮🇹

Pisa, Italy

Fukuoka University Hospital /ID# 254729

🇯🇵

Fukuoka-shi, Fukuoka, Japan

Meiwa Hospital /ID# 254728

🇯🇵

Nishinomiya-shi, Hyogo, Japan

University of Tsukuba Hospital /ID# 254638

🇯🇵

Tsukuba-shi, Ibaraki, Japan

University Hospital Kyoto Prefectural University of Medicine /ID# 254481

🇯🇵

Kyoto-shi, Kyoto, Japan

Tohoku University Hospital /ID# 254598

🇯🇵

Sendai-shi, Miyagi, Japan

University of the Ryukyus Hospital /ID# 254517

🇯🇵

Nakagami-gun, Okinawa, Japan

Kindai University Hospital /ID# 254574

🇯🇵

Osakasayama-shi, Osaka, Japan

Shiga University of Medical Science Hospital /ID# 254215

🇯🇵

Otsu, Shiga, Japan

Nihon University Itabashi Hospital /ID# 254637

🇯🇵

Itabashi-ku, Tokyo, Japan

Toranomon Hospital /ID# 253819

🇯🇵

Minato-ku, Tokyo, Japan

Korea University Ansan Hospital /ID# 254128

🇰🇷

Ansan-si, Gyeonggido, Korea, Republic of

CHA Bundang Medical Center /ID# 254026

🇰🇷

Seongnam, Gyeonggido, Korea, Republic of

Seoul National University Hospital /ID# 254027

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

SoonChunHyang University Seoul Hospital /ID# 254025

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Hallym University Kangnam Sacred Heart Hospital /ID# 254127

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Inlita Santara CTC /ID# 253917

🇱🇹

Vilnius, Lithuania

Vilnius University Hospital Santaros Klinikos /ID# 253916

🇱🇹

Vilnius, Lithuania

Amphia Ziekenhuis /ID# 253567

🇳🇱

Breda, Noord-Brabant, Netherlands

Universitair Medisch Centrum Groningen /ID# 253571

🇳🇱

Groningen, Netherlands

Greenlane Clinical Centre /ID# 254351

🇳🇿

Epsom, Auckland, New Zealand

Clinical Trials New Zealand /ID# 254352

🇳🇿

Hamilton, Waikato, New Zealand

Hospital CUF Descobertas /ID# 254323

🇵🇹

Lisboa, Portugal

Centro Hospitalar de Lisboa Central /ID# 254325

🇵🇹

Lisbon, Portugal

Centro Hospitalar Universitario do Porto, EPE - Hospital Santo Antonio /ID# 254322

🇵🇹

Porto, Portugal

Centro Hospitalar Universitario de Sao Joao, EPE /ID# 254324

🇵🇹

Porto, Portugal

Dr. Samuel Sanchez PSC /ID# 253948

🇵🇷

Caguas, Puerto Rico

Alma M. Cruz Santana, MD-Private practice /ID# 253951

🇵🇷

Carolina, Puerto Rico

King Faisal Specialist Hospital and Research Centre /ID# 255279

🇸🇦

Riyadh, Ar Riyad, Saudi Arabia

King Abdulaziz Medical City- National Guard Hospital /ID# 255280

🇸🇦

Riyadh, Ar Riyad, Saudi Arabia

King Faisal Specialist Hospital /ID# 255539

🇸🇦

Jeddah, Makkah, Saudi Arabia

King Saud University Med City /ID# 255282

🇸🇦

Riyadh, Saudi Arabia

National Skin Centre /ID# 255242

🇸🇬

Singapore, Central Singapore, Singapore

National University Hospital /ID# 254943

🇸🇬

Singapore, Singapore

Univerzitná nemocnica Bratislava - Nemocnica Ružinov /ID# 254157

🇸🇰

Bratislava, Bratislavsky Kraj, Slovakia

Univerzitna nemocnica L. Pasteura Kosice /ID# 254136

🇸🇰

Košice, Kosicky Kraj, Slovakia

Fakultna nemocnica s poliklinikou Nove Zamky /ID# 254155

🇸🇰

Nove Zamky, Nitriansky Kraj, Slovakia

Univerzitna nemocnica Martin /ID# 254153

🇸🇰

Martin, Zilinsky Kraj, Slovakia

Fakultna nemocnica Trnava /ID# 254137

🇸🇰

Trnava, Slovakia

Hospital Universitari de Bellvitge /ID# 254982

🇪🇸

L'Hospitalet de Llobregat, Barcelona, Spain

Hospital Universitario Puerta de Hierro - Majadahonda /ID# 253924

🇪🇸

Majadahonda, Madrid, Spain

Hospital de Manises /ID# 253867

🇪🇸

Manises, Valencia, Spain

Hospital Santa Creu i Sant Pau /ID# 253869

🇪🇸

Barcelona, Spain

Hospital General de Granollers /ID# 253873

🇪🇸

Barcelona, Spain

Hospital Universitario Virgen de las Nieves /ID# 253870

🇪🇸

Granada, Spain

Hospital Universitario Ramon y Cajal /ID# 253871

🇪🇸

Madrid, Spain

Hospital Universitario y Politecnico La Fe /ID# 253868

🇪🇸

Valencia, Spain

Karolinska University Hospital Solna /ID# 254808

🇸🇪

Solna, Stockholms Lan, Sweden

Sahlgrenska Universitetssjukhuset /ID# 254807

🇸🇪

Göteborg, Vastra Gotalands Lan, Sweden

Kantonsspital St. Gallen /ID# 255243

🇨🇭

St. Gallen, Sankt Gallen, Switzerland

University Hospital Zurich /ID# 254642

🇨🇭

Zurich, Zuerich, Switzerland

Inselspital, Universitaetsspital Bern /ID# 254736

🇨🇭

Bern, Switzerland

Kaohsiung Chang Gung Memorial Hospital /ID# 254031

🇨🇳

Kaohsiung City, Kaohsiung, Taiwan

National Taiwan University Hospital /ID# 254030

🇨🇳

Taipei City, Taipei, Taiwan

Changhua Christian Hospital /ID# 254032

🇨🇳

Changhua City, Changhua County, Taiwan

Linkou Chang Gung Memorial Hospital /ID# 254033

🇨🇳

Taoyuan City, Taiwan

Gulhane Egitim ve Arastirma Hastanesi /ID# 253919

🇹🇷

Ankara, Turkey

Uludag University Medical Faculty /ID# 253806

🇹🇷

Bursa, Turkey

Istanbul Universitesi-Cerrahpasa Cerrahpasa Tip Fakultesi /ID# 253824

🇹🇷

Istanbul, Turkey

Erciyes University Medical Faculty /ID# 253804

🇹🇷

Kayseri, Turkey

Ondokuz Mayis Universitesi /ID# 254034

🇹🇷

Samsun, Turkey

Chelsea and Westminster Hospital /ID# 254190

🇬🇧

London, Greater London, United Kingdom

University Hospital Southampton NHS Foundation Trust /ID# 254531

🇬🇧

Southampton, Hampshire, United Kingdom

UH Coventry & Warwickshire /ID# 256909

🇬🇧

Coventry, Warwickshire, United Kingdom

Leeds Teaching Hospitals NHS Trust /ID# 254616

🇬🇧

Leeds, West Yorkshire, United Kingdom

Northern Care Alliance NHS Group /ID# 256910

🇬🇧

Salford, United Kingdom

St George's University Hospitals NHS Foundation Trust /ID# 256803

🇬🇧

Tooting, United Kingdom

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