MedPath

Study of Oral Navitoclax Tablet in Combination With Oral Ruxolitinib Tablet to Assess Change in Spleen Volume in Adult Participants With Relapsed/Refractory Myelofibrosis

Phase 3
Active, not recruiting
Conditions
Myelofibrosis (MF)
Interventions
Drug: Best Available Therapy (BAT)
Drug: Navitoclax
Drug: Ruxolitinib
Registration Number
NCT04468984
Lead Sponsor
AbbVie
Brief Summary

Myelofibrosis (MF) is a rare blood cancer, notable for scarring of the bone marrow (the spongy tissue inside bones) and the spleen becoming larger. The purpose of this study is to assess safety and change in spleen volume when navitoclax is given in combination with ruxolitinib, compared to best available therapy, for adult participants with MF.

Navitoclax is an investigational drug (not yet approved) being developed for the treatment of MF. Participants in this study will be randomly selected (like picking numbers out of a hat) to be in 1 of 2 treatment arms. Neither participants nor the study doctor will be able to pick which treatment arm a participants enters. In Arm A, participants will receive navitoclax in combination with ruxolitinib. In Arm B, participants will receive the best available therapy (BAT) for MF. Adult participants with a diagnosis of MF that came back or did not get better after earlier treatment will be enrolled. Approximately 330 participants will be enrolled in approximately 210 sites across the world.

In Arm A, participants will receive navitoclax tablet by mouth once daily with by mouth ruxolitinib tablet twice daily. In Arm B, participants will receive the BAT available to the investigator. Participants will receive the study drug until they experience no benefit (determined by the investigator), participants cannot tolerate the study drugs, or participants withdraw consent. The approximate treatment duration is about 3 years.

There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of treatment will be checked by medical assessments, blood and bone marrow tests, checking for side effects, and completing questionnaires.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
295
Inclusion Criteria
  • Must complete the Myelofibrosis Symptom Assessment Form (MFSAF) v4.0 on at least 4 out of the 7 days immediately prior to the date of randomization and must agree to collect MFSAF data daily by ePRO device during the study collection window.

    -- Has at least 2 symptoms each with an average score >= 3 or an average total score of >= 12, as measured by the MFSAF v4.0.

  • Documented diagnosis of primary myelofibrosis (MF) as defined by the World Health Organization (WHO) classification, post polycythemia vera (PPV)-MF, or post essential thrombocytopenia (PET)-MF, characterized by bone marrow fibrosis grades 2 or 3.

  • Classified as intermediate-2 or high-risk MF, as defined by the Dynamic International Prognostic Scoring System Plus (DIPSS+).

  • Must currently be on treatment or have received prior treatment with a single Janus Kinase 2 (JAK2) inhibitor, ruxolitinib, and meet one of the following criteria (in addition to the minimum splenomegaly and symptom burden also required for eligibility):

    • Treatment with ruxolitinib for >= 24 weeks that was stopped due to lack of spleen response (refractory), or loss of spleen response or symptom control after a previous response (relapsed), or was continued despite relapsed/refractory status.

    • Treatment with ruxolitinib for < 24 weeks with documented disease progression while on therapy as defined by any of the following:

      • Appearance of new splenomegaly that is palpable to at least 5 cm below the left costal margin (LCM) in participants with no evidence of splenomegaly prior to the initiation of ruxolitinib.
      • A >= 100% increase in the palpable distance below the LCM in participants with measurable spleen distance 5 to 10 centimeters (cm) prior to the initiation of ruxolitinib.
      • A >= 50% increase in the palpable distance below the LCM in participants with measurable spleen distance > 10 cm prior to the initiation of ruxolitinib.
      • A spleen volume increase of >= 25% (as assessed by Magnetic Resonance Imaging [MRI] or Computed Tomography [CT] scan) in participants with a spleen volume assessment prior to the initiation of ruxolitinib.
    • Prior treatment with ruxolitinib of at least 10 mg twice daily (BID) for >= 28 days with intolerance defined as new RBC transfusion requirement (at least 2 units/month for 2 months) while receiving a total daily ruxolitinib dose of >= 30 mg but unable to reduce dose further due to lack of efficacy.

Note: Participant must not require a ruxolitinib dose less than 10 mg BID (20 mg daily) due to prior history of ruxolitinibrelated ≥ Grade 3 toxicity.

  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
  • Splenomegaly defined as palpable spleen measurement >= 5 cm below left costal margin or spleen volume >= 450 cm3 as assessed centrally by MRI or CT scan.
  • Baseline platelet count >= 100 × 10^9/L.
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Exclusion Criteria
  • Received prior treatment with a BH3-mimetic compound, bromodomain and extra-terminal (BET) inhibitor, or prior use of > 1 JAK2 inhibitor or stem cell transplant.
  • Eligible for stem cell transplantation at the time of study entry.
  • Receiving medication that interferes with coagulation or platelet function within 3 days prior to the first dose of study drug or during the study treatment period except for low dose aspirin (up to 100 mg daily) and low molecular weight heparin (LMWH).
  • Receiving anticancer therapy for an active malignancy or MF including chemotherapy, radiation therapy, hormonal therapy such that at least 5 half-lives of that medication is completed at least 7 days prior to the first dose of study drug or within 30 days prior to first dose of study drug, whichever is shorter, and during the study treatment period (other than any overlapping therapy as part of the selected BAT).
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm B: Best Available Therapy (BAT)Best Available Therapy (BAT)Participants will receive one of the BAT options, per the investigator's discretion.
Arm A: Navitoclax + RuxolitinibNavitoclaxParticipants will receive navitoclax tablets once daily and ruxolitinib tablets twice daily.
Arm A: Navitoclax + RuxolitinibRuxolitinibParticipants will receive navitoclax tablets once daily and ruxolitinib tablets twice daily.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants who achieve Spleen Volume Reduction of at least 35% at Week 24 (SVR35W24)At Week 24

Reduction in spleen volume is measured by Magnetic Resonance Imaging (MRI) or Computed Tomography (CT), per International Working Group (IWG) criteria.

Secondary Outcome Measures
NameTimeMethod
Percentage of Participants with Overall SurvivalLast Visit Up to 5 Years

Overall survival is defined as the time from start of study to the date of death from any cause.

Percentage of Participants with Anemia ResponseBaseline (Week 0) Up to Week 97

Anemia response per International Working Group (IWG) criteria will be assessed.

Percentage of Participants with Change in FatigueBaseline (Week 0) Up to Week 24

Change in fatigue will be assessed using the Patient Reported Outcomes Measurement Information System (PROMIS) Fatigue Short Form (SF) 7a.

Percentage of Participants who achieve at least 50% Reduction in Total Symptom Score (TSS)Baseline (Week 0) Up to Week 24

Reduction in TSS is measured by Myelofibrosis Symptom Assessment Form (MFSAF) v4.0.

Percentage of Participants who achieve Spleen Volume Reduction of at least 35% at any timeBaseline (Week 0) Up to Week 97

Reduction in spleen volume is measured by Magnetic Resonance Imaging (MRI) or Computed Tomography (CT), per International Working Group (IWG) criteria.

Percentage of Participants with Reduction in Grade of Bone Marrow FibrosisBaseline (Week 0) Up to Week 97

Reduction in grade of bone marrow fibrosis from baseline as measured by the European consensus grading system will be assessed.

Percentage of Participants with Leukemia-free SurvivalLast Visit Up to 5 Years

Leukemia free survival is the time from start of study to the date of development of leukemia.

Time to Deterioration of Physical FunctioningBaseline (Week 0) Up to Week 97

Time to deterioration of physical functioning is measured by the physical functioning domain of the European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ)-C30, or death.

Percentage of Participants with at Least 50% Reduction in TSSBaseline (Week 0) Up to Week 97

At least 50% reduction in TSS from baseline (at any time) as measured by MFSAF v4.0.

Trial Locations

Locations (215)

Hospital of the University of Pennsylvania /ID# 219001

🇺🇸

Philadelphia, Pennsylvania, United States

Princess Margaret Cancer Centre /ID# 253942

🇨🇦

Toronto, Ontario, Canada

Klinikum Wels-Grieskirchen GmbH /ID# 220915

🇦🇹

Wels, Oberoesterreich, Austria

UMHAT Dr Georgi Stranski EAD /ID# 231650

🇧🇬

Pleven, Bulgaria

CISSS-CA (Centre Integre de sante et de services sociaux de Chaudiere-Appalache) /ID# 222433

🇨🇦

Levis, Quebec, Canada

Chu de Nice-Hopital Larchet Ii /Id# 256291

🇫🇷

Nice, Alpes-Maritimes, France

CHU NIMES - Hopital Caremeau /ID# 219128

🇫🇷

Nimes CEDEX 9, Gard, France

Centre Hospitalier Métropole Savoie - Site Hôpital de Chambéry /ID# 223771

🇫🇷

Chambery CEDEX, Savoie, France

CHU de Nantes, Hotel Dieu -HME /ID# 219127

🇫🇷

Nantes, Pays-de-la-Loire, France

Olympion General Clinic /ID# 261423

🇬🇷

Patras, Achaia, Greece

Fejér Vármegyei Szent György Egyetemi Oktató Kórház /ID# 220949

🇭🇺

Szekesfehervar, Fejer, Hungary

Szabolcs-Szatmar-Bereg Varmegyei Oktatokorhaz /ID# 220946

🇭🇺

Nyiregyhaza, Szabolcs-Szatmar-Bereg, Hungary

Szegedi Tudományegyetem /ID# 220955

🇭🇺

Szeged, Hungary

HaEmek Medical Center /ID# 220839

🇮🇱

Afula, H_efa, Israel

Rambam Health Care Campus /ID# 219121

🇮🇱

Haifa, H_efa, Israel

Yitzhak Shamir Medical Center /ID# 222972

🇮🇱

Zerifin, HaMerkaz, Israel

Galilee Medical Center /ID# 225280

🇮🇱

Nahariya, HaTsafon, Israel

The Chaim Sheba Medical Center /ID# 219136

🇮🇱

Ramat Gan, Tel-Aviv, Israel

Tel Aviv Sourasky Medical Center /ID# 219135

🇮🇱

Tel Aviv, Tel-Aviv, Israel

Hadassah Medical Center-Hebrew University /ID# 219111

🇮🇱

Jerusalem, Yerushalayim, Israel

Hadassah Mt. Scopus /ID# 253394

🇮🇱

Jerusalem, Yerushalayim, Israel

Rabin Medical Center /ID# 219139

🇮🇱

Haifa, Israel

Azienda Ospedaliero Universitaria Ospedali Riuniti Do Ancona /ID# 238438

🇮🇹

Torette, Ancona, Italy

Fondazione Policlinico Universitario Agostino Gemelli IRCCS-Universita Cattolica /ID# 219087

🇮🇹

Rome, Lazio, Italy

Fujita Health University Hospital /ID# 221598

🇯🇵

Toyoake, Aichi, Japan

Aomori Prefectural Central Hospital /ID# 221778

🇯🇵

Aomori-shi, Aomori, Japan

Kobe City Medical Center General Hospital /ID# 221156

🇯🇵

Kobe-shi, Hyogo, Japan

Kanazawa University Hospital /ID# 223028

🇯🇵

Kanazawa-shi, Ishikawa, Japan

Mie University Hospital /ID# 221665

🇯🇵

Tsu-shi, Mie, Japan

Niigata University Medical & Dental Hospital /ID# 223034

🇯🇵

Niigata-shi, Niigata, Japan

Osaka University Hospital /ID# 221159

🇯🇵

Suita-shi, Osaka, Japan

SP ZOZ Szpital Uniwersytecki w Krakowie /ID# 221160

🇵🇱

Krakow, Malopolskie, Poland

Szpital Kliniczny im. Heliodora Swiecickiego Uniwersytetu Medycznego im. Karola /ID# 241031

🇵🇱

Poznan, Wielkopolskie, Poland

Almazov National Medical Research Centre /ID# 221114

🇷🇺

Sankt-Peterburg, Russian Federation

Nippon Medical School Hospital /ID# 221676

🇯🇵

Bunkyo-ku, Tokyo, Japan

University of Yamanashi Hospital /ID# 221706

🇯🇵

Chuo-shi, Yamanashi, Japan

IMSUT Hospital, The Institute of Medical Science, The University of Tokyo /ID# 257944

🇯🇵

Tokyo, Japan

Wojewódzkie Wielospecjalistyczne Centrum Onkologii i Traumatologii im. M. Kopern /ID# 221161

🇵🇱

Lodz, Lodzkie, Poland

University Clinical Center Serbia /ID# 231058

🇷🇸

Belgrade, Beograd, Serbia

University Clinical Center Vojvodina /ID# 231057

🇷🇸

Novi Sad, Serbia

Kaohsiung Medical University Chung-Ho Memorial Hospital /ID# 218980

🇨🇳

Kaohsiung, Taiwan

Dana-Farber Cancer Institute /ID# 218998

🇺🇸

Boston, Massachusetts, United States

MetroHealth Medical Center /ID# 222650

🇺🇸

Cleveland, Ohio, United States

Columbus Regional Research Institute /ID# 224410

🇺🇸

Columbus, Georgia, United States

Cliniques Universitaires UCL Saint-Luc /ID# 224221

🇧🇪

Woluwe-Saint-Lambert, Bruxelles-Capitale, Belgium

UZ Gent /ID# 220841

🇧🇪

Gent, Oost-Vlaanderen, Belgium

Vitaz /Id# 228150

🇧🇪

Sint-Niklaas, Belgium

Acibadem City Clinic Tokuda University Hospital EAD /ID# 231649

🇧🇬

Sofia, Bulgaria

Hopital Avicenne - APHP /ID# 221287

🇫🇷

Bobigny, Ile-de-France, France

Universitaetsmedizin Rostock /ID# 224157

🇩🇪

Rostock, Mecklenburg-Vorpommern, Germany

BAG Freiberg-Richter, Jacobasch, Illmer, Wolf /ID# 221346

🇩🇪

Dresden, Sachsen, Germany

Ordensklinikum Linz GmbH Elisabethinen /ID# 220914

🇦🇹

Linz, Oberoesterreich, Austria

Medizinische Universitaet Graz /ID# 220919

🇦🇹

Graz, Steiermark, Austria

Ottawa Hospital Research Institute /ID# 238858

🇨🇦

Ottawa, Ontario, Canada

Medizinische Universitaet Wien /ID# 220911

🇦🇹

Vienna, Wien, Austria

UMHAT Alexandrovska EAD /ID# 231652

🇧🇬

Sofiya, Sofia, Bulgaria

Virginia Cancer Specialists - Fairfax /ID# 223016

🇺🇸

Fairfax, Virginia, United States

ZNA Cadix /ID# 221468

🇧🇪

Antwerp, Antwerpen, Belgium

AZ-Delta /ID# 221469

🇧🇪

Roeselare, West-Vlaanderen, Belgium

UMHAT Sveti Ivan Rilski /ID# 231651

🇧🇬

Sofia, Bulgaria

HSHS St. Vincent Hospital /ID# 224468

🇺🇸

Green Bay, Wisconsin, United States

Border Medical Oncology Research Unit Albury Wodonga Regiona /ID# 223848

🇦🇺

East Albury, New South Wales, Australia

Juravinski Cancer Centre /ID# 220887

🇨🇦

Hamilton, Ontario, Canada

The Alfred Hospital /ID# 221096

🇦🇺

Melbourne, Victoria, Australia

Yakima Valley Memorial Hosp /ID# 224368

🇺🇸

Yakima, Washington, United States

Universitaetsklinikum St. Poelten /ID# 221709

🇦🇹

Sankt Poelten, Niederoesterreich, Austria

Hanusch Krankenhaus /ID# 220912

🇦🇹

Wien, Austria

Grand Hopital de Charleroi /ID# 224827

🇧🇪

Charleroi, Hainaut, Belgium

UMHAT Sveta Marina /ID# 234119

🇧🇬

Varna, Bulgaria

Providence Everett /ID# 223130

🇺🇸

Everett, Washington, United States

The Kinghorn Cancer Centre /ID# 221097

🇦🇺

Darlinghurst, New South Wales, Australia

Augusta-Kranken-Anstalt gGmbH, Bochum-Mitte /ID# 224695

🇩🇪

Bochum, Germany

Fakultni nemocnice Brno /ID# 220959

🇨🇿

Brno, Czechia

HCL - Hopital Lyon Sud /ID# 222695

🇫🇷

Pierre Benite CEDEX, Rhone, France

Calvary Mater Newcastle /ID# 224324

🇦🇺

Waratah, New South Wales, Australia

Tula Regional Clinical Hospital /ID# 221302

🇷🇺

Tula, Russian Federation

McGill University Health Center Research Institute /ID# 222614

🇨🇦

Montreal, Quebec, Canada

Klinicka bolnica Merkur /ID# 230799

🇭🇷

Zagreb, Grad Zagreb, Croatia

Klinicki bolnicki centar Osijek /ID# 231503

🇭🇷

Osijek, Croatia

Universitatsklinikum Mannheim /ID# 221529

🇩🇪

Mannheim, Baden-Wuerttemberg, Germany

Stauferklinikum Schwaebisch Gmuend /ID# 223948

🇩🇪

Mutlangen, Baden-Wuerttemberg, Germany

Klinikum Chemnitz gGmbH /ID# 224575

🇩🇪

Chemnitz, Germany

Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII (Presidio Papa Giovanni /ID# 221222

🇮🇹

Bergamo, Italy

ASST Sette Laghi /ID# 234183

🇮🇹

Varese, Italy

Clinical Hospital Dubrava /ID# 230801

🇭🇷

Zagreb, Grad Zagreb, Croatia

Klinicki bolnicki centar Zagreb /ID# 230798

🇭🇷

Zagreb, Grad Zagreb, Croatia

University General Hospital of Patras /ID# 221178

🇬🇷

RION Patras Achaia, Greece

AP-HP - Hopital Saint-Louis /ID# 221390

🇫🇷

Paris, France

OncoResearch Lerchenfeld GmbH /ID# 225034

🇩🇪

Hamburg, Germany

Vseobecna fakultni nemocnice v Praze /ID# 220969

🇨🇿

Praha, Czechia

Klinicki Bolnicki Centar (KBC) Split /ID# 230800

🇭🇷

Split, Splitsko-dalmatinska Zupanija, Croatia

Centre Hospitalier Universitaire de Bordeaux /ID# 222696

🇫🇷

Pessac CEDEX, Gironde, France

Debreceni Egyetem-Klinikai Kozpont /ID# 220947

🇭🇺

Debrecen, Hajdu-Bihar, Hungary

ASST Monza/Ospedale San Gerardo /ID# 225113

🇮🇹

Monza, Monza E Brianza, Italy

Chu Angers /Id# 219129

🇫🇷

Angers, France

Gemeinschaftspraxis Dr. Heinrich und Prof. Bangerter /ID# 225025

🇩🇪

Augsburg, Bayern, Germany

General Hospital of Athens Laiko /ID# 221175

🇬🇷

Athens, Attiki, Greece

General Hospital of Athens Evaggelismos and Ophthalmiatrio of Athens Polyclinic /ID# 221179

🇬🇷

Athens, Greece

General Hospital of Thessaloniki George Papanikolaou /ID# 221463

🇬🇷

Thessaloniki, Greece

Somogy Varmegyei Kaposi Mor Oktato Korhaz /ID# 220948

🇭🇺

Kaposvár, Somogy, Hungary

Ehime University Hospital /ID# 221158

🇯🇵

Toon-shi, Ehime, Japan

Sapporo Hokuyu Hospital /ID# 221149

🇯🇵

Sapporo-shi, Hokkaido, Japan

Iwate Medical University Hospital /ID# 222044

🇯🇵

Shiwa-gun, Iwate, Japan

Samsung Medical Center /ID# 221091

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

The Lady Davis Carmel Medical Center /ID# 222973

🇮🇱

Haifa, H_efa, Israel

Assuta Ashdod Medical Center /ID# 225281

🇮🇱

Ashdod, HaDarom, Israel

Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital /ID# 221150

🇯🇵

Nagoya-shi, Aichi, Japan

Sapienza University /ID# 225731

🇮🇹

Rome, Roma, Italy

IRCCS Azienda Ospedaliero-Universitaria di Bologna /ID# 221077

🇮🇹

Bologna, Italy

Azienda Ospedaliera Universitaria Paolo Giaccone /ID# 221078

🇮🇹

Palermo, Italy

Chiba University Hospital /ID# 224546

🇯🇵

Chiba-shi, Chiba, Japan

Kyushu University Hospital /ID# 221606

🇯🇵

Fukuoka-shi, Fukuoka, Japan

Fukushima Medical University Hospital /ID# 221877

🇯🇵

Fukushima-shi, Fukushima, Japan

Kumamoto Shinto General Hospital /ID# 255645

🇯🇵

Kumamoto-shi, Kumamoto, Japan

Kyoto University Hospital /ID# 223008

🇯🇵

Kyoto-shi, Kyoto, Japan

Uniwersyteckie Centrum Kliniczne /ID# 221298

🇵🇱

Gdansk, Pomorskie, Poland

Pratia Onkologia Katowice /ID# 224526

🇵🇱

Katowice, Poland

Presidio Ospedaliero Gaspare Rodolico /ID# 219089

🇮🇹

Catania, Italy

Pusan National University Hospital /ID# 220980

🇰🇷

Busan, Busan Gwang Yeogsi, Korea, Republic of

Hospital Universitario La Paz /ID# 224813

🇪🇸

Madrid, Spain

National Cancer Center Hospital East /ID# 226653

🇯🇵

Kashiwa-shi, Chiba, Japan

Azienda Ospedaliero Universitaria Careggi /ID# 219090

🇮🇹

Florence, Italy

Shonan Kamakura General Hospital /ID# 223030

🇯🇵

Kamakura-shi, Kanagawa, Japan

Lux Med Onkologia - Szpital Szamocka /Id# 221265

🇵🇱

Warszawa, Mazowieckie, Poland

Azienda Ospedaliera Universitaria Federico II /ID# 224673

🇮🇹

Napoli, Italy

Gachon University Gil Medical Center /ID# 220972

🇰🇷

Incheon, Gyeonggido, Korea, Republic of

Azienda ULSS 8 Berica/Ospedale San Bortolo di Vicenza /ID# 221079

🇮🇹

Vicenza, Italy

Gifu University Hospital /ID# 224371

🇯🇵

Gifu-shi, Gifu, Japan

University of Miyazaki Hospital /ID# 221821

🇯🇵

Miyazaki-shi, Miyazaki, Japan

Dokkyo Medical University Saitama Medical Center /ID# 222334

🇯🇵

Koshigaya, Saitama, Japan

Hospital Clinico Universitario de Valencia /ID# 220920

🇪🇸

Valencia, Spain

Uniwersytecki Szpital Kliniczny Nr 1 w Lublinie /ID# 221124

🇵🇱

Lublin, Lubelskie, Poland

MTZ Clinical Research Powered by Pratia /ID# 221759

🇵🇱

Warszawa, Mazowieckie, Poland

ARS-MEDICAL Sp. z o.o. /ID# 238336

🇵🇱

Pila, Wielkopolskie, Poland

Tokyo Metropolitan Bokutoh Hospital /ID# 254774

🇯🇵

Sumida-ku, Tokyo, Japan

Hospital Parc de Salut del Mar /ID# 220922

🇪🇸

Barcelona, Spain

Aotearoa Clinical Trials /ID# 232201

🇳🇿

Papatoetoe, Auckland, New Zealand

Duplicate_Wits Clinical Research Site /ID# 231554

🇿🇦

Johannesburg, Gauteng, South Africa

Moscow State budget healthcare /ID# 221116

🇷🇺

Moscow, Moskva, Russian Federation

Hospital Universitario Vall d'Hebron /ID# 240979

🇪🇸

Barcelona, Spain

United Lincolnshire Hospitals NHS Trust /ID# 224613

🇬🇧

Lincoln, Lincolnshire, United Kingdom

Alberts Cellular Therapy /ID# 231556

🇿🇦

Pretoria, Gauteng, South Africa

Trakya University Medical Facu /ID# 224572

🇹🇷

Edirne, Istanbul, Turkey

Complejo Hospitalario Universitario A Coruña /ID# 224617

🇪🇸

A Coruña, A Coruna, Spain

Hospital n.a. V.V. Veresaev /ID# 225221

🇷🇺

Moscow, Russian Federation

Russian Research Institute of Hematology and Transfusiology of the FMBA /ID# 221115

🇷🇺

Sankt-Peterburg, Russian Federation

Hospital Universitario Central de Asturias /ID# 224815

🇪🇸

Oviedo, Asturias, Spain

Inselspital, Universitaetsspital Bern /ID# 223439

🇨🇭

Bern, Switzerland

China Medical University Hospital /ID# 218979

🇨🇳

Taichung, Taiwan

The Newcastle Upon Tyne Hospitals NHS Foundation Trust /ID# 221335

🇬🇧

Newcastle upon Tyne, United Kingdom

Hospital Clínico Universitario de Santiago-CHUS /ID# 221616

🇪🇸

Santiago de Compostela, A Coruna, Spain

Hospital Universitario Virgen de las Nieves /ID# 253936

🇪🇸

Granada, Spain

Hospital Universitario Dr. Negrin /ID# 220923

🇪🇸

Las Palmas de Gran Canaria, Las Palmas, Spain

Taipei Veterans General Hosp /ID# 221147

🇨🇳

Taipei, Taiwan

Kaohsiung Chang Gung Memorial Hospital /ID# 218985

🇨🇳

Kaohsiung City, Kaohsiung, Taiwan

Chi Mei Hospital - Liouying /ID# 221144

🇨🇳

Tainan City, Taiwan

Linkou Chang Gung Memorial Hospital /ID# 218982

🇨🇳

Taoyuan City, Taiwan

James Paget University Hospitals NHS Foundation Trust /ID# 221219

🇬🇧

Great Yarmouth, Norfolk, United Kingdom

Gulhane Askeri Tip Academy /ID# 224568

🇹🇷

Ankara, Turkey

NHS Lothian /ID# 224378

🇬🇧

Edinburgh, United Kingdom

Hospital Universitario Virgen del Rocio /ID# 221932

🇪🇸

Sevilla, Spain

Hospital Regional Universitario de Malaga /ID# 221906

🇪🇸

Malaga, Spain

Mersin University Medical /ID# 224571

🇹🇷

Mersin, Turkey

University Hospitals Birmingham NHS Foundation Trust /ID# 221334

🇬🇧

Birmingham, United Kingdom

Ondokuz mayis University Facul /ID# 224567

🇹🇷

Samsun, Turkey

Royal Perth Hospital /ID# 221099

🇦🇺

Perth, Western Australia, Australia

Duplicate_Universitätsspital Basel /ID# 221261

🇨🇭

Basel, Basel-Stadt, Switzerland

Aalborg University Hospital /ID# 224391

🇩🇰

Aalborg, Nordjylland, Denmark

Roskilde Sygehus /ID# 224456

🇩🇰

Roskilde, Sjælland, Denmark

Skane University Hospital Lund /ID# 220834

🇸🇪

Lund, Skane Lan, Sweden

Ege University Medical Faculty /ID# 224570

🇹🇷

Izmir, Turkey

Guys and St Thomas NHS Foundation Trust /ID# 221041

🇬🇧

London, London, City Of, United Kingdom

Klinikum rechts der Isar /ID# 221526

🇩🇪

Munich, Germany

Hospital Universitario Germans Trias i Pujol /ID# 233727

🇪🇸

Badalona, Barcelona, Spain

Hospital Universitario 12 de Octubre /ID# 233726

🇪🇸

Madrid, Spain

Hospital Universitario de Salamanca /ID# 221904

🇪🇸

Salamanca, Spain

The Catholic University of Korea, Seoul St. Marys Hospital /ID# 219061

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Utah Cancer Specialists Salt Lake Clinic /ID# 221962

🇺🇸

Salt Lake City, Utah, United States

University of Michigan /ID# 218463

🇺🇸

Ann Arbor, Michigan, United States

Indiana Blood & Marrow Transpl /ID# 221587

🇺🇸

Indianapolis, Indiana, United States

Atrium Health Wake Forest Baptist Medical Center /ID# 222899

🇺🇸

Winston-Salem, North Carolina, United States

University of Texas Health San Antonio MD Anderson Cancer Center /ID# 233942

🇺🇸

San Antonio, Texas, United States

Moores Cancer Center at UC San Diego /ID# 219009

🇺🇸

La Jolla, California, United States

Ironwood Cancer & Res Ctr /ID# 222162

🇺🇸

Chandler, Arizona, United States

Long Beach Memorial Medical Ct /ID# 224542

🇺🇸

Long Beach, California, United States

Highlands Oncology Group, PA /ID# 221826

🇺🇸

Springdale, Arkansas, United States

Icri /Id# 221967

🇺🇸

Whittier, California, United States

Augusta University Georgia Cancer Center /ID# 219051

🇺🇸

Augusta, Georgia, United States

St. Mary's Hospital Regional Cancer Center /ID# 224229

🇺🇸

Grand Junction, Colorado, United States

Northwest Oncology & Hematology - Elk Grove Village /ID# 222818

🇺🇸

Elk Grove Village, Illinois, United States

American Oncology Partners of Maryland /ID# 222836

🇺🇸

Bethesda, Maryland, United States

William Beaumont Hospital /ID# 222705

🇺🇸

Royal Oak, Michigan, United States

Henry Ford Health System /ID# 221190

🇺🇸

Detroit, Michigan, United States

Saint Louis University Cancer Center /ID# 222287

🇺🇸

Saint Louis, Missouri, United States

Memorial Sloan Kettering Cancer Center-Koch Center /ID# 221081

🇺🇸

New York, New York, United States

The Cancer Institute at St. Francis Hospital /ID# 231782

🇺🇸

Greenvale, New York, United States

Summit Medical Group-Florham Park /ID# 222620

🇺🇸

Florham Park, New Jersey, United States

Hackensack Univ Med Ctr /ID# 219047

🇺🇸

Hackensack, New Jersey, United States

Manhattan Hematology Oncology MHO Associates /ID# 223193

🇺🇸

New York, New York, United States

Fox Chase Cancer Center /ID# 223955

🇺🇸

Philadelphia, Pennsylvania, United States

Duplicate_Houston Methodist Hospital /ID# 223103

🇺🇸

Houston, Texas, United States

AOU Citta della Salute e della Scienza di Torino /ID# 221223

🇮🇹

Torino, Piemonte, Italy

Azienda Ospedaliera Universitaria Friuli Centrale/Presidio Ospedaliero Universit /ID# 221241

🇮🇹

Udine, Italy

Grande Ospedale Metropolitano Bianchi Melacrino Morelli /ID# 221220

🇮🇹

Reggio Calabria, Italy

Juntendo University Hospital /ID# 221154

🇯🇵

Bunkyo-ku, Tokyo, Japan

Kurashiki Central Hospital /ID# 221690

🇯🇵

Kurashiki-shi, Okayama, Japan

Kansai Medical University Hospital /ID# 257289

🇯🇵

Hirakata-shi, Osaka, Japan

Juntendo University Shizuoka Hospital /ID# 221780

🇯🇵

Izunokuni-shi, Shizuoka, Japan

Seoul National University Hospital /ID# 219060

🇰🇷

Seoul, Seoul Teugbyeolsi, Korea, Republic of

Clin Hosp Ctr Bezanijska Kosa /ID# 231059

🇷🇸

Belgrade, Beograd, Serbia

Hospital del Centro Comprensivo de Cancer de la UPR /ID# 223281

🇵🇷

San Juan, Puerto Rico

Loyola University Medical Ctr /ID# 219048

🇺🇸

Maywood, Illinois, United States

Tulane Medical Center - New Orleans /ID# 222940

🇺🇸

New Orleans, Louisiana, United States

Ochsner Clinic Foundation-New Orleans /ID# 222777

🇺🇸

New Orleans, Louisiana, United States

Tokyo Medical University Hospital /ID# 221540

🇯🇵

Shinjuku-ku, Tokyo, Japan

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