MedPath

A Study Evaluating Safety and Efficacy of Venetoclax in Combination With Azacitidine Versus Standard of Care After Allogeneic Stem Cell Transplantation (SCT) in Participants With Acute Myeloid Leukemia (AML)

Phase 3
Active, not recruiting
Conditions
Acute Myeloid Leukemia (AML)
Cancer
Interventions
Other: Best Supportive Care (BSC)
Registration Number
NCT04161885
Lead Sponsor
AbbVie
Brief Summary

The main objective of this study is to evaluate the efficacy of venetoclax in combination with azacitidine to improve Overall Survival (OS) in Acute Myeloid Leukemia (AML) participants compared to Best Supportive Care (BSC) when given as maintenance therapy following allogeneic stem cell transplantation (SCT).

This study will have 2 parts: Part 1 (Dose Confirmation), which may include participants who are greater than or equal to 18 years old; Part 2 (Randomization) which may include participants who are greater than or equal to 12 years old. During Part 1, recommended Phase 3 dose of venetoclax in combination with azacitidine will be determined and during Part 2, the efficacy and safety of venetoclax with azacitidine (Part 2 Arm A) will be compared with BSC (Part 2 Arm B).

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
465
Inclusion Criteria
  • Participants must be at least 18 years old for Part 1 and, at least 12 years old for Part 2.
  • Participant must be diagnosed with Acute Myeloid Leukemia (AML) by World Health Organization (WHO) criteria (2017) and either be planning for allogeneic stem cell transplantation or have received allogeneic stem cell transplantation within the past 60 days.
  • Blast percentage in bone marrow before transplant must be < 10%.
  • Blast count in peripheral blood must be "0" and Blast percentage in bone marrow must be < 5% after transplant.
  • Participant meet adequate renal, hepatic and hematologic criteria as described in the protocol.
  • Participants >= 17 years old must have a Karnofsky Performance Scale (KPS) score > 50 and participants between 12 to 16 years old must have a Lansky Play Performance Scale score > 40.
Exclusion Criteria
  • History of disease progression during prior treatment with venetoclax.
  • History of any other malignancy within 2 years prior to study entry, except for: Adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of breast; basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin; previous malignancy confined and surgically resected (or treated with other modalities) with curative intent; Myelodysplastic Syndrome, Myeloproliferative neoplasm (only allowed if it transformed to AML and AML should be the indication for marrow transplantation).
  • Participant has known infection with HIV or history of being positive for hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
  • Presence of clinical or laboratory symptoms/signs of extramedullary myeloid malignancy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Part 1: Venetoclax + Azacitidine (AZA) + Best Supportive CareBest Supportive Care (BSC)Participants will be administered various doses and dose regiments of venetoclax and AZA. Venetoclax will be administered once daily (QD) (Days 1-28) for up to 24 cycles, AZA QD on Days 1-5 of each 28-day cycle for up to 6 cycles and best supportive care (BSC) for 24 cycles (each cycle = 28 days)
Part 2: Arm B - Best Supportive Care (BSC)Best Supportive Care (BSC)Participants will receive treatment as prescribed by their physician according to the BSC for up to 24 cycles (1 cycle = 28 days)
Part 2: Arm A - Venetoclax + Azacitidine (AZA) + BSCBest Supportive Care (BSC)Participants will be administered with venetoclax and AZA at a dose level determined in Part 1 in addition to best supportive care (when required). Venetoclax will be administered once daily (QD) (Days 1-28) for up to 24 cycles, AZA QD on Days 1-5 of each 28-day cycle for up to 6 cycles and best supportive care (BSC) for 24 cycles (each cycle = 28 days).
Part 1: Venetoclax + Azacitidine (AZA) + Best Supportive CareVenetoclaxParticipants will be administered various doses and dose regiments of venetoclax and AZA. Venetoclax will be administered once daily (QD) (Days 1-28) for up to 24 cycles, AZA QD on Days 1-5 of each 28-day cycle for up to 6 cycles and best supportive care (BSC) for 24 cycles (each cycle = 28 days)
Part 1: Venetoclax + Azacitidine (AZA) + Best Supportive CareAzacitidineParticipants will be administered various doses and dose regiments of venetoclax and AZA. Venetoclax will be administered once daily (QD) (Days 1-28) for up to 24 cycles, AZA QD on Days 1-5 of each 28-day cycle for up to 6 cycles and best supportive care (BSC) for 24 cycles (each cycle = 28 days)
Part 2: Arm A - Venetoclax + Azacitidine (AZA) + BSCVenetoclaxParticipants will be administered with venetoclax and AZA at a dose level determined in Part 1 in addition to best supportive care (when required). Venetoclax will be administered once daily (QD) (Days 1-28) for up to 24 cycles, AZA QD on Days 1-5 of each 28-day cycle for up to 6 cycles and best supportive care (BSC) for 24 cycles (each cycle = 28 days).
Part 2: Arm A - Venetoclax + Azacitidine (AZA) + BSCAzacitidineParticipants will be administered with venetoclax and AZA at a dose level determined in Part 1 in addition to best supportive care (when required). Venetoclax will be administered once daily (QD) (Days 1-28) for up to 24 cycles, AZA QD on Days 1-5 of each 28-day cycle for up to 6 cycles and best supportive care (BSC) for 24 cycles (each cycle = 28 days).
Primary Outcome Measures
NameTimeMethod
Number of Participants With Dose-Limiting Toxicities (DLTs) Following Administration of Venetoclax and Azacitidine (Part 1)Up to the first treatment cycle (28 days)

DLTs are any of the hematologic, nonhematologic toxicities, adverse events (AEs) occurring following administration of venetoclax and AZA as described in the protocol and evaluated by the Investigator and the sponsor.

Overall Survival (OS) (Part 2)Up to 45 months after the first participant is randomized

OS is defined as the number of days from the date of randomization to the date of death from any cause.

Secondary Outcome Measures
NameTimeMethod
Composite Relapse-Free Survival (RFS) (Part 2)Up to 39 months after the first participant is randomized

Morphologic relapse from AML, non-morphologic relapse from AML, which is defined as increase in disease burden determined by standard methods with reappearance or acquisition of new findings with or without change in anti-leukemic treatment per investigator decision due to cytogenetic abnormalities or change in molecular marker or measurable residual disease by multiparameter flow with sensitivity to at least 10\^-3; or the date of death from any cause, whichever comes first as determined by IRC.

Graft-versus-Host Disease (GvHD)-free, Relapse Free Survival (GRFS) (Part 2)Up to 39 months after the first participant is randomized

GRFS is defined as number of days from the date of randomization to occurrence of disease relapse OR incidence of GvHD OR death from any cause.

Graft-versus-Host Disease (GvHD) Rate (Part 2)Up to 39 months after the first participant is randomized

GvHD rate is defined as grade 2 or higher for acute graft-versus-host disease (aGvHD) and moderate/severe for chronic graft-versus-host disease (cGvHD) assessed by investigator.

Change in Patient Reported Signs, Symptoms and Impact of Acute Myeloid Leukemia (AML) as Measured by the European Quality-of-Life-5 Dimensional-5-Level (EQ-5D-5L)Up to 39 months after the first participant is randomized

The EQ-5D-5L is a generic preference instrument that has been validated in numerous population and has 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. These dimensions are measured on a 5-point scale: with higher scores representing better functioning/quality of life and greater symptom burden.

Measurable Residual Disease (MRD) Response Rate in Participants With MRD >= 10^-3 at Randomization (Part 2)Up to 39 months after the first participant is randomized

MRD conversion rate is defined as percentage of participants who convert to MRD \< 10\^-3 after initiation of treatment.

Change From Randomization in Fatigue in Adult Participants (Part 2)Up to 39 months after the first participant is randomized

Fatigue is measured as Patient Reported Outcome (PRO) using Patient Reported Outcomes Measurement Information System (PROMIS) Cancer Fatigue SF 7a.

Change from Baseline in Physical Functioning as Measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC-QLQ-C30) (Part 2)Up to 39 months after the first participant is randomized

The EORTC-QLQ-C30 is a 30-item patient-reported questionnaire composed of both multi-item and single scales including 5 functional scales (physical, role, emotional, social, and cognitive), 3 symptom scales (fatigue, nausea and vomiting, and pain), a global health status/QoL scale, and 6 single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, and financial difficulties). Participantts rate items on a 4-point scale ranging from 1 to 4 (1 = Not at All, 2 = A Little, 3 = Quite a Bit, and 4 = Very Much).

Time to Deterioration in Global Health Status (GHS)/Quality of Life (QoL) in Adult Participants (Part 2)Up to 39 months after the first participant is randomized

Time to deterioration defined as number of days from randomization to either deterioration of \>= 5 points based on the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) version 3 or death due to any cause.

Morphologic Relapse-Free Survival (RFS) (Part 2)Up to 39 months after the first participant is randomized

Morphologic relapse from AML defined as bone marrow blasts of \>= 5% or reappearance of blasts in the peripheral blood not attributable to any other cause (e.g., bone marrow regeneration) in at least 2 peripheral blood samples at least one week apart or development of extramedullary disease after achieving a complete remission (CR) or complete remission with incomplete count recovery (CRi); or the date of death from any cause, whichever comes first as determined by Independent Review Committee (IRC).

Trial Locations

Locations (165)

Hospital Clinico Universitario de Valencia /ID# 215106

🇪🇸

Valencia, Spain

Hospital Universitario Virgen del Rocio /ID# 215463

🇪🇸

Sevilla, Spain

Arizona Oncology - Scottsdale - Cancer Transplant Institute /ID# 239711

🇺🇸

Scottsdale, Arizona, United States

University of Arizona Cancer Center - Tucson /ID# 242507

🇺🇸

Tucson, Arizona, United States

University of Arkansas for Medical Sciences /ID# 239804

🇺🇸

Little Rock, Arkansas, United States

City of Hope /ID# 213681

🇺🇸

Duarte, California, United States

UCHSC Anschultz Cancer Pavilion /ID# 215618

🇺🇸

Aurora, Colorado, United States

Colorado Blood Cancer Institute /ID# 215980

🇺🇸

Denver, Colorado, United States

Mayo Clinic /ID# 239710

🇺🇸

Jacksonville, Florida, United States

AdventHealth Medical Group Blood & Marrow Transplant at Orlando /ID# 213985

🇺🇸

Orlando, Florida, United States

Ann & Robert H Lurie Children's Hospital of Chicago /ID# 215840

🇺🇸

Chicago, Illinois, United States

The University of Chicago Medical Center /ID# 215616

🇺🇸

Chicago, Illinois, United States

Loyola University Medical Ctr /ID# 215617

🇺🇸

Maywood, Illinois, United States

Indiana Blood & Marrow Transpl /ID# 215842

🇺🇸

Indianapolis, Indiana, United States

Duplicate_Ochsner Clinic Foundation-New Orleans /ID# 213834

🇺🇸

New Orleans, Louisiana, United States

University of Maryland, Baltimore /ID# 213855

🇺🇸

Baltimore, Maryland, United States

Massachusetts General Hospital /ID# 215765

🇺🇸

Boston, Massachusetts, United States

Karmanos Cancer Institute - Dresner Clinic /ID# 214581

🇺🇸

Detroit, Michigan, United States

Masonic Cancer Center /ID# 239492

🇺🇸

Minneapolis, Minnesota, United States

Mayo Clinic - Rochester /ID# 214685

🇺🇸

Rochester, Minnesota, United States

University of Mississippi Medical Center /ID# 239343

🇺🇸

Jackson, Mississippi, United States

The John Theurer Cancer /ID# 215251

🇺🇸

Hackensack, New Jersey, United States

Montefiore Medical Center - Moses Campus /ID# 241669

🇺🇸

Bronx, New York, United States

Roswell Park Cancer Institute /ID# 217857

🇺🇸

Buffalo, New York, United States

Columbia University Medical Center /ID# 240875

🇺🇸

New York, New York, United States

Memorial Sloan Kettering Cancer Center-Koch Center /ID# 240680

🇺🇸

New York, New York, United States

Weill Cornell Medical College /ID# 214887

🇺🇸

New York, New York, United States

University of North Carolina /ID# 215814

🇺🇸

Chapel Hill, North Carolina, United States

Wake Forest Univ HS /ID# 239210

🇺🇸

Winston-Salem, North Carolina, United States

UC Health - Cincinnati /ID# 239263

🇺🇸

Cincinnati, Ohio, United States

University Hospitals - Seidman Cancer Center /ID# 239260

🇺🇸

Cleveland, Ohio, United States

University of Oklahoma, Stephenson Cancer Center /ID# 215611

🇺🇸

Oklahoma City, Oklahoma, United States

Oregon Health and Science University /ID# 215874

🇺🇸

Portland, Oregon, United States

Penn State Hershey Medical Ctr /ID# 217120

🇺🇸

Hershey, Pennsylvania, United States

Children's Hospital of Philadelphia - Main /ID# 215410

🇺🇸

Philadelphia, Pennsylvania, United States

Perelman Center for Advanced Medicine /ID# 214518

🇺🇸

Philadelphia, Pennsylvania, United States

Duplicate_Allegheny General Hospital /ID# 216756

🇺🇸

Pittsburgh, Pennsylvania, United States

UPMC Hillman Cancer Ctr /ID# 213715

🇺🇸

Pittsburgh, Pennsylvania, United States

TriStar Centennial Medical Center /ID# 218750

🇺🇸

Nashville, Tennessee, United States

Texas Oncology - Medical City Dallas /ID# 216720

🇺🇸

Dallas, Texas, United States

Texas Oncology- Baylor Charles A. Sammons Cancer Center /ID# 213735

🇺🇸

Dallas, Texas, United States

Texas Transplant Institute /ID# 214691

🇺🇸

San Antonio, Texas, United States

Virginia Commonwealth University Medical Center Main Hospital /ID# 239203

🇺🇸

Richmond, Virginia, United States

Fred Hutchinson Cancer Research Center /ID# 214436

🇺🇸

Seattle, Washington, United States

Univ of Wisconsin Hosp/Clinics /ID# 216096

🇺🇸

Madison, Wisconsin, United States

The Kinghorn Cancer Centre /ID# 214660

🇦🇺

Darlinghurst, New South Wales, Australia

Royal Adelaide Hospital /ID# 215678

🇦🇺

Adelaide, South Australia, Australia

Peter MacCallum Cancer Ctr /ID# 214653

🇦🇺

Melbourne, Victoria, Australia

The Alfred Hospital /ID# 240931

🇦🇺

Melbourne, Victoria, Australia

Hospital de Clinicas de Porto Alegre /ID# 215042

🇧🇷

Porto Alegre, Rio Grande Do Sul, Brazil

Hospital Amaral Carvalho - Fundacao Doutor Amaral Carvalho /ID# 215145

🇧🇷

Jaú, Sao Paulo, Brazil

Hospital Nove de Julho /ID# 242359

🇧🇷

São Paulo, Sao Paulo, Brazil

Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao /ID# 239516

🇧🇷

Sao Paulo, Brazil

Vancouver Coastal Health Research Institute (VCHRI) /ID# 215363

🇨🇦

Vancouver, British Columbia, Canada

University Health Network_Princess Margaret Cancer Centre /ID# 215344

🇨🇦

Toronto, Ontario, Canada

CIUSSS de l'est de l'Ile-de-Montreal - Hopital Maisonneuve-Rosemont /ID# 214591

🇨🇦

Montreal, Quebec, Canada

Royal Victoria Hospital / McGill University Health Centre /ID# 215253

🇨🇦

Montreal, Quebec, Canada

Saskatoon Cancer Centre /ID# 238821

🇨🇦

Saskatoon, Saskatchewan, Canada

Peking University People's Hospital /ID# 215551

🇨🇳

Beijing, Beijing, China

Chinese PLA General Hospital /ID# 216287

🇨🇳

Beijing, Beijing, China

Aerospace Center Hospital /ID# 217018

🇨🇳

Beijing, Beijing, China

Fujian Medical University Union Hospital /ID# 215555

🇨🇳

Fuzhou, Fujian, China

Guangdong Provincial People's Hospital /ID# 218666

🇨🇳

Guangzhou, Guangdong, China

Zhujiang Hospital of Southern Medical University /ID# 216333

🇨🇳

Guangzhou, Guangdong, China

Nanfang Hospital of Southern Medical University /ID# 215553

🇨🇳

Guangzhou, Guangdong, China

Shenzhen Second People's Hospital /ID# 239401

🇨🇳

Shenzhen, Guangdong, China

Henan Cancer Hospital /ID# 215554

🇨🇳

Zhengzhou, Henan, China

Tongji Hospital Tongji Medical College Huazhong University of Science and Techno /ID# 215552

🇨🇳

Wuhan, Hubei, China

Union Hospital Tongji Medical College Huazhong University of Science and Technol /ID# 238373

🇨🇳

Wuhan, Hubei, China

Xiangya Hospital Central South University /ID# 219025

🇨🇳

Changsha, Hunan, China

Zhongda Hospital Southeast University /ID# 218926

🇨🇳

Nanjing, Jiangsu, China

The First Affiliated Hospital of Soochow University /ID# 216605

🇨🇳

Suzhou, Jiangsu, China

The Affiliated Hospital of Xuzhou Medical College /ID# 239098

🇨🇳

Xuzhou, Jiangsu, China

The First Affiliated Hospital of Nanchang University /ID# 239168

🇨🇳

Nanchang, Jiangxi, China

Shanghai Changhai Hospital /ID# 216334

🇨🇳

Shanghai, Shanghai, China

Tangdu Hospital of The Fourth Military Medical University, PLA /ID# 216282

🇨🇳

Xi'an, Shanxi, China

Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sc /ID# 215546

🇨🇳

Tianjin, Tianjin, China

The First Affiliated Hospital, Zhejiang University School of Medicine /ID# 215550

🇨🇳

Hangzhou, Zhejiang, China

Fakultní Nemocnice Brno - Jihlavská /ID# 214811

🇨🇿

Brno, Brno-mesto, Czechia

Fakultní nemocnice Hradec Králové - Sokolská /ID# 214814

🇨🇿

Hradec Králové, Hradec Kralove, Czechia

Fakultni Nemocnice Ostrava /ID# 239922

🇨🇿

Ostrava, Ostrava-mesto, Czechia

Ustav hematologie a krevni transfuze /ID# 215133

🇨🇿

Praha, Czechia

Duplicate_CHU de Nice - Hôpital Archet 1 /ID# 214056

🇫🇷

Nice, Alpes-Maritimes, France

CHU de Besancon - Jean Minjoz /ID# 241171

🇫🇷

Besancon, Doubs, France

Duplicate_CHU Bordeaux - Hopital Haut Leveque /ID# 214055

🇫🇷

Pessac, Gironde, France

Hopital Pitie Salpetriere /ID# 241072

🇫🇷

Paris Cedex 13, Ile-de-France, France

CHRU Lille - Hopital Claude Huriez /ID# 217916

🇫🇷

Lille, Nord, France

CHU de Nantes, Hotel Dieu -HME /ID# 214060

🇫🇷

Nantes, Pays-de-la-Loire, France

Hôpital Saint-Louis /ID# 214054

🇫🇷

Paris, France

AP-HP - Hopital Saint-Antoine /ID# 216957

🇫🇷

Paris, France

Universitaetsklinik Heidelberg /ID# 216623

🇩🇪

Heidelberg, Baden-Wuerttemberg, Germany

Klinikum Augsburg /ID# 239583

🇩🇪

Augsburg, Bayern, Germany

Universitaetsklinikum Wuerzburg /ID# 215212

🇩🇪

Wuerzburg, Bayern, Germany

Universitaetsklinikum Muenster /ID# 215213

🇩🇪

Muenster, Nordrhein-Westfalen, Germany

Universitaetsklinikum Carl Gustav Carus Dresden /ID# 214244

🇩🇪

Dresden, Sachsen, Germany

Universitaetsklinikum Leipzig /ID# 245892

🇩🇪

Leipzig, Sachsen, Germany

Universitaetsklinikum Halle (Saale) /ID# 239585

🇩🇪

Halle (Saale), Germany

Medizinische Hochschule Hannover /ID# 214243

🇩🇪

Hannover, Germany

General Hospital of Athens Evangelismos /ID# 238810

🇬🇷

Athens, Attiki, Greece

University General Hospital Attikon /ID# 238812

🇬🇷

Athens, Attiki, Greece

University General Hospital of Patras /ID# 238811

🇬🇷

RION Patras Achaia, Greece

Debreceni Egyetem-Klinikai Kozpont /ID# 241123

🇭🇺

Debrecen, Hajdu-Bihar, Hungary

Rambam Health Care Campus /ID# 214507

🇮🇱

Haifa, H_efa, Israel

Schneider Children's Medical Center /ID# 224326

🇮🇱

Petah Tikva, HaMerkaz, Israel

Sheba Medical Center /ID# 239571

🇮🇱

Ramat Gan, Tel-Aviv, Israel

The Chaim Sheba Medical Center /ID# 214305

🇮🇱

Ramat Gan, Tel-Aviv, Israel

Tel Aviv Sourasky Medical Center /ID# 214508

🇮🇱

Tel Aviv, Tel-Aviv, Israel

Hadassah Medical Center-Hebrew University /ID# 218697

🇮🇱

Jerusalem, Yerushalayim, Israel

Rabin Medical Center /ID# 214509

🇮🇱

Petah Tikva, Israel

IRCCS Ospedale San Raffaele /ID# 214311

🇮🇹

Milan, Milano, Italy

Istituto Europeo Di Oncologia /ID# 242579

🇮🇹

Milan, Milano, Italy

A.O.U. CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO - Ospedale Molinette /ID# 216148

🇮🇹

Torino, Piemonte, Italy

Azienda Ospedaliero-Universitaria Policlinico Umberto I /ID# 254964

🇮🇹

Rome, Roma, Italy

Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Università Cattolica /ID# 214910

🇮🇹

Rome, Roma, Italy

ASST degli Spedali Civili di Brescia /ID# 215997

🇮🇹

Brescia, Italy

Anjou Kousei Hospital /ID# 215857

🇯🇵

Anjo-shi, Aichi, Japan

Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital /ID# 215679

🇯🇵

Nagoya-shi, Aichi, Japan

University of Fukui Hospital /ID# 253383

🇯🇵

Yoshida-gun, Fukui, Japan

Kyushu University Hospital /ID# 215285

🇯🇵

Fukuoka-shi, Fukuoka, Japan

Fukushima Medical University Hospital /ID# 252293

🇯🇵

Fukushima-shi, Fukushima, Japan

Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital /ID# 217522

🇯🇵

Hiroshima-shi, Hiroshima, Japan

Hokkaido University Hospital /ID# 215937

🇯🇵

Sapporo-shi, Hokkaido, Japan

Kobe City Medical Center General Hospital /ID# 215388

🇯🇵

Kobe-shi, Hyogo, Japan

Hyogo Medical University Hospital /ID# 215389

🇯🇵

Nishinomiya-shi, Hyogo, Japan

Kanazawa University Hospital /ID# 242955

🇯🇵

Kanazawa-shi, Ishikawa, Japan

Imamura General Hospital /ID# 215688

🇯🇵

Kagoshima-shi, Kagoshima, Japan

Tokai University Hospital /ID# 250086

🇯🇵

Isehara, Kanagawa, Japan

Kanagawa Cancer Center /ID# 215029

🇯🇵

Yokohama-shi, Kanagawa, Japan

Kyoto University Hospital /ID# 243209

🇯🇵

Kyoto-shi, Kyoto, Japan

Tohoku University Hospital /ID# 214670

🇯🇵

Sendai-shi, Miyagi, Japan

Okayama University Hospital /ID# 214842

🇯🇵

Okayama-shi, Okayama, Japan

Osaka Metropolitan University Hospital /ID# 215227

🇯🇵

Osaka-shi, Osaka, Japan

Kindai University Hospital /ID# 214917

🇯🇵

Osakasayama-shi, Osaka, Japan

Jichi Medical University Saitama Medical Center /ID# 216092

🇯🇵

Saitama-shi, Saitama, Japan

Jichi Medical University Hospital /ID# 216091

🇯🇵

Shimotsuke-shi, Tochigi, Japan

Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital /ID# 215939

🇯🇵

Bunkyo-ku, Tokyo, Japan

National Cancer Center Hospital /ID# 242639

🇯🇵

Chuo-ku, Tokyo, Japan

Toranomon Hospital /ID# 215311

🇯🇵

Minato-ku, Tokyo, Japan

National Center for Child Health and Development /ID# 242479

🇯🇵

Setagaya-ku, Tokyo, Japan

Keio University Hospital /ID# 243549

🇯🇵

Shinjuku-ku, Tokyo, Japan

Yamagata University Hospital /ID# 253304

🇯🇵

Yamagata-shi, Yamagata, Japan

Seoul National University Hospital /ID# 214891

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Asan Medical Center /ID# 214893

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Samsung Medical Center /ID# 239087

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

The Catholic University of Korea, Seoul St. Marys Hospital /ID# 214892

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Hospital Clinic de Barcelona /ID# 215108

🇪🇸

Barcelona, Spain

Hospital Santa Creu i Sant Pau /ID# 240397

🇪🇸

Barcelona, Spain

Hospital General Universitario Gregorio Maranon /ID# 215107

🇪🇸

Madrid, Spain

Hospital Universitario Ramon y Cajal /ID# 218102

🇪🇸

Madrid, Spain

Hospital Universitario La Paz /ID# 218103

🇪🇸

Madrid, Spain

Duplicate_Universitätsspital Basel /ID# 215892

🇨🇭

Basel, Basel-Stadt, Switzerland

University Hospital Zurich /ID# 215891

🇨🇭

Zurich, Zuerich, Switzerland

National Taiwan University Hospital /ID# 215245

🇨🇳

Taipei City, Taipei, Taiwan

Kaohsiung Medical University Chung-Ho Memorial Hospital /ID# 215197

🇨🇳

Kaohsiung, Taiwan

China Medical University Hospital /ID# 215198

🇨🇳

Taichung, Taiwan

Taichung Veterans General Hospital /ID# 239288

🇨🇳

Taichung, Taiwan

Taipei Veterans General Hosp /ID# 239289

🇨🇳

Taipei, Taiwan

Linkou Chang Gung Memorial Hospital /ID# 215319

🇨🇳

Taoyuan City, Taiwan

Hammersmith Hospital /ID# 215665

🇬🇧

London, England, United Kingdom

Gartnavel General Hospital /ID# 215663

🇬🇧

Glasgow, Glasgow City, United Kingdom

University College London Hospital /ID# 215662

🇬🇧

London, Greater London, United Kingdom

University Hospitals Birmingham NHS Foundation Trust /ID# 215120

🇬🇧

Birmingham, United Kingdom

The Royal Marsden NHS Foundation Trust /ID# 215124

🇬🇧

London, United Kingdom

The Newcastle Upon Tyne Hospitals NHS Foundation Trust /ID# 248359

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Newcastle upon Tyne, United Kingdom

King's College Hospital NHS Foundation Trust /ID# 215338

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London, United Kingdom

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