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A Trial to Learn if Odronextamab is Safe and Well-Tolerated and How Well it Works Compared to Rituximab Combined With Different Types of Chemotherapy for Participants With Follicular Lymphoma

Phase 3
Recruiting
Conditions
Follicular Lymphoma (FL)
Interventions
Registration Number
NCT06091254
Lead Sponsor
Regeneron Pharmaceuticals
Brief Summary

This study is researching an experimental drug called odronextamab, referred to as study drug. The study is focused on participants with previously untreated follicular lymphoma (a type of non-Hodgkin lymphoma or NHL).

This study will be made up of two parts: Part 1 (non-randomized) and Part 2 (randomized - controlled).

The aim of Part 1 of the study is to see how safe and tolerable the study drug is when given alone.

The aim of Part 2 of the study is to see how the study drug works compared to rituximab (called the "comparator drug") and chemotherapy (the current standard of care for NHL). Standard of care means the usual medication expected and used when receiving treatment for a condition.

The study is looking at several other research questions, including:

* What side effects may happen from taking the study drug

* How much study drug is in the blood at different times

* Whether the body makes antibodies against the study drug (which could make the study drug less effective or could lead to side effects)

* How the study drug affects quality of life and ability to complete routine daily activities.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
478
Inclusion Criteria
  1. Diagnosis of Cluster of Differentiation 20^+ (CD20^+) FL Grade 1-3a, stage II bulky or stage III / IV
  2. Need for treatment as described in the protocol
  3. Have measurable disease on cross-sectional imaging documented by diagnostic imaging Computed Tomography (CT) or Magnetic Resonance Imaging (MRI)
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  5. Adequate bone marrow function and hepatic function

Key

Exclusion Criteria
  1. Central Nervous System (CNS) lymphoma or leptomeningeal lymphoma
  2. Histological evidence of transformation to a high-grade or diffuse large B-cell lymphoma
  3. Waldenström Macroglobulinemia (WM, lymphoplasmacytic lymphoma), Grade 3b follicular lymphoma, chronic lymphocytic leukemia, or small lymphocytic lymphoma
  4. Treatment with any systemic anti-lymphoma therapy
  5. Infections and allergy/hypersensitivity to study drug or excipient

NOTE: Other protocol defined inclusion/exclusion criteria apply

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
OdronextamabOdronextamabPart 1 is a safety run-in. All participants will receive odronextamab. In part 2 participants will be randomly assigned in a 1:1 ratio to receive odronextamab followed by odronextamab maintenance.
Rituximab + Investigator's Choice ChemotherapyRituximabPart 2 only, participants will be randomized 1:1 to receive rituximab in combination with chemotherapy followed by rituximab maintenance.
Rituximab + Investigator's Choice ChemotherapyDoxorubicinPart 2 only, participants will be randomized 1:1 to receive rituximab in combination with chemotherapy followed by rituximab maintenance.
Rituximab + Investigator's Choice ChemotherapyPrednisone/prednisolonePart 2 only, participants will be randomized 1:1 to receive rituximab in combination with chemotherapy followed by rituximab maintenance.
Rituximab + Investigator's Choice ChemotherapyBendamustinePart 2 only, participants will be randomized 1:1 to receive rituximab in combination with chemotherapy followed by rituximab maintenance.
Rituximab + Investigator's Choice ChemotherapyCyclophosphamidePart 2 only, participants will be randomized 1:1 to receive rituximab in combination with chemotherapy followed by rituximab maintenance.
Rituximab + Investigator's Choice ChemotherapyVincristinePart 2 only, participants will be randomized 1:1 to receive rituximab in combination with chemotherapy followed by rituximab maintenance.
Primary Outcome Measures
NameTimeMethod
Incidence of treatment-emergent adverse events (TEAEs) of odronextamabUp to 2 years

Part 1

Incidence of dose-limiting toxicities (DLTs) for odronextamabUp to 35 days

Part 1

Complete Response at 30 months (CR30) as assessed by independent central reviewUp to 30 months

Part 2

Severity of TEAEs of odronextamabUp to 2 years

Part 1

Secondary Outcome Measures
NameTimeMethod
Objective response as assessed by the investigatorUp to 30 months

Part 1

Concentrations of odronextamab in serumUp to 30 months

Part 1

Titer of ADAs to odronextamab over the study durationUp to 30 months

Part 2

Incidence of NAbs to odronextamab over the study durationUp to 30 months

Part 2

Overall mean changes in scores of PROs, as measured by the validated instruments Patient Global Impression of Change (PGIC)Up to 5 years

Part 2 The PGIC item includes a single-item to assess how a patient perceives their overall change in health status since the start of study treatment. Patients will choose from response options on a 7-point scale ranging from 1 (Much Better) to 7 (Much worse); 1- Much Better, 2-Moderately Better, 3-A Little Better, 4-About the Same, 5-A Little Worse, 6-Moderately Worse, 7-Much Worse.

Progression-free survival (PFS) as assessed by independent central reviewUp to 5 years

Part 2

CR30 as assessed by local investigatorUp to 30 months

Part 2

Overall survival (OS)Up to 5 years

Part 2

Duration of response (DOR) assessed by independent central reviewUp to 5 years

Part 2

Incidence of TEAEsUp to 2 years

Part 2

Incidence of anti-drug antibodies (ADAs) to odronextamab over the study durationUp to 30 months

Part 1

Event-free survival (EFS) as assessed by independent central reviewUp to 5 years

Part 2

PFS as assessed by the local investigatorUp to 5 years

Part 2

Odronextamab concentrations in serum during the induction periodUp to 30 months

Part 2

Incidence of ADAs to odronextamab over the study durationUp to 30 months

Part 2

Change in score of the GP5 item in the participant populationUp to 5 years

Part 2 A single item Global Population item 5 (GP5) of the validated FACT-G questionnaire will be used to assess from the participant perspective the overall impact of treatment side-effect. The question item is on a 5-point scale ranging from "not at all" (0) to "very much" (4).

Incidence of neutralizing antibodies (NAbs) to odronextamab over the study durationUp to 30 months

Part 1

Overall mean change in physical function [European Organization for Research and Treatment of Cancer Quality of Life Core Questionnaire 30 (EORTC-QLQ-C30)]Up to 5 years

Part 2 The EORTC QLQ-C30 includes 5 functional scales (physical, role, cognitive, emotional and social functioning), 3 symptom scales (fatigue, pain and nausea/vomiting), a global health status (GHS)/QoL scale, and six single items (constipation, diarrhea, insomnia, shortness of breath, appetite loss and financial difficulties). For the functioning scales and global health status / QoL, scores range from 1 = "very poor" to 7 = "excellent" with higher scores indicate better functioning; for the symptom scales, scores range from 1 = "not at all" to 4 = "very much" higher scores indicate higher symptom burden.

Objective response assessed by independent central reviewUp to 30 months

Part 2

DOR assessed by local investigatorUp to 5 years

Part 2

Time to next anti-lymphoma treatment (TTNT)Up to 5 years

Part 2

Severity of TEAEsUp to 2 years

Part 2

Odronextamab concentrations in serum during the maintenance periodUp to 30 months

Part 2

Overall mean changes in scores of patient reported outcomes (PROs), as measured by the validated instruments EORTCQLQ- C30Up to 5 years

Part 2 The EORTC QLQ-C30 includes 5 functional scales (physical, role, cognitive, emotional and social functioning), 3 symptom scales (fatigue, pain and nausea/vomiting), a global health status (GHS)/QoL scale, and six single items (constipation, diarrhea, insomnia, shortness of breath, appetite loss and financial difficulties). For the functioning scales and global health status / QoL, scores range from 1 = "very poor" to 7 = "excellent" with higher scores indicate better functioning; for the symptom scales, scores range from 1 = "not at all" to 4 = "very much" higher scores indicate higher symptom burden.

Overall mean changes in scores of PROs, as measured by the validated instruments EuroQol-5 Dimension-5 Level Scale (EQ-5D- 5L)Up to 5 years

Part 2 The EQ-5D-5L consists of the EQ-5D descriptive system and the EQ visual analogue scale (EQ VAS). The EQ-5D-5L descriptive system comprises the following 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: "no problems", "slight problems", "moderate problems", "severe problems" and "extreme problems". The EQ VAS records the participant's self-rated health on a vertical visual analogue scale where the endpoints are labeled "Best imaginable health state" and "Worst imaginable health state".

EFS as assessed by the local investigatorUp to 5 years

Part 2

Objective response assessed by local investigatorUp to 30 months

Part 2

Overall mean changes in scores of PROs, as measured by the validated instruments Functional Assessment of Cancer Therapy-Lymphoma (FACT-LymS)Up to 5 years

Part 2 The FACT-Lym lymphoma subscale (LymS) includes 15 items to assess NHL-related symptoms and concerns. All questions are answered on a 5-point scale ranging from "not at all" (0) to "very much" (4). Higher scores are associated with a worse quality of life.

Overall mean changes in scores of PROs, as measured by the validated instruments Patient Global Impression of Severity (PGIS)Up to 5 years

Part 2 The PGIS includes a single-item to assess how a patient perceives the overall severity of cancer symptoms over the past 7 days. Patients will choose the response that best describes the severity of their overall cancer symptoms with options on a 5-point scale ranging from 1 (No symptoms) to 4 (Very Severe).

Overall mean changes in scores PROs, as measured by the validated Functional Assessment of Cancer - General (FACT-G) global population 5 (GP5) questionUp to 5 years

Part 2 A single item GP5 of the validated FACT-G questionnaire will be used to assess from the participant perspective the overall impact of treatment side-effect. The question item is on a 5-point scale ranging from "not at all" (0) to "very much" (4).

Trial Locations

Locations (171)

University of Arizona Cancer Center

🇺🇸

Tucson, Arizona, United States

HOPE Cancer Center of East Texas

🇺🇸

Tyler, Texas, United States

David Geffen School of Medicine at UCLA

🇺🇸

Los Angeles, California, United States

UC Irvine Health

🇺🇸

Orange, California, United States

Investigative Clinical Research of Indiana

🇺🇸

Noblesville, Indiana, United States

Beth Israel Deaconess Medical Center

🇺🇸

Boston, Massachusetts, United States

Karmanos Cancer Institute

🇺🇸

Detroit, Michigan, United States

Icahn School of Medicine at Mt Sinai

🇺🇸

New York, New York, United States

Stony Brook University Hospital

🇺🇸

Stony Brook, New York, United States

Clinical Research Alliance Inc

🇺🇸

Westbury, New York, United States

Institut Jules Bordet

🇧🇪

Brussels, Belgium

University of North Carolina

🇺🇸

Chapel Hill, North Carolina, United States

Levine Cancer Institute

🇺🇸

Charlotte, North Carolina, United States

University of Virginia

🇺🇸

Charlottesville, Virginia, United States

Prohealth Care Inc

🇺🇸

Waukesha, Wisconsin, United States

Ingham Institute

🇦🇺

Liverpool, New South Wales, Australia

University Hospitals Cleveland Medical Center

🇺🇸

Cleveland, Ohio, United States

Center for Oncology and Blood Disorders

🇺🇸

Houston, Texas, United States

Icon Cancer Centre - Wesley

🇦🇺

Auchenflower, Queensland, Australia

Flinders Medical Centre

🇦🇺

Bedford Park, South Australia, Australia

Monash Health

🇦🇺

Clayton, Victoria, Australia

Instituto DOr de Pesquisa e Ensino Df Star

🇧🇷

Brasilia, Brazil

Epworth Freemasons

🇦🇺

East Melbourne, Victoria, Australia

St Vincent's Hospital - Melbourne

🇦🇺

Fitzroy, Victoria, Australia

Alfred Hospital and Monash University

🇦🇺

Melbourne, Victoria, Australia

Ordensklinikum Linz

🇦🇹

Linz, Osterreich, Austria

Ordensklinikum Linz Gmbh, Elisabethinen

🇦🇹

Linz, Austria

Uniklinikum Salzburg (LKH) Universitatsklinik fur Innere Medizin III

🇦🇹

Salzburg, Austria

Medical University of Vienna

🇦🇹

Vienna, Austria

Hanusch Krankenhaus

🇦🇹

Vienna, Austria

AZ St.-Elisabeth Herentals vzw

🇧🇪

Herentals, Antwerp, Belgium

Instituto Mario Pena de Ensino Pesquisa e Inovacao

🇧🇷

Belo Horizonte, Minas Gerais, Brazil

Liga Norte Riograndense Contra o Cancer

🇧🇷

Natal, Rio Grande Do Norte, Brazil

Instituto do Cancer em Hospital Sao Vicente de Paulo

🇧🇷

Passo Fundo, Rio Grande Do Sul, Brazil

Centro de Hematologia e Oncologia

🇧🇷

Joinville, Santa Catarina, Brazil

Amaral Carvalho Hospital

🇧🇷

Jau, Sao Paulo, Brazil

Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto da Universidade de Sao Paulo

🇧🇷

Ribeirao Preto, Sao Paulo, Brazil

Animi Unidade de Tratamento Oncologico Ltda

🇧🇷

Lages, Brazil

Hospital de Clinicas de Porto Alegre

🇧🇷

Porto Alegre, Brazil

Instituto Americas

🇧🇷

Rio de Janeiro, Brazil

Hospital Alemao Oswaldo Cruz

🇧🇷

Sao Paulo, Brazil

AC Camargo Cancer Center

🇧🇷

Sao Paulo, Brazil

Casa de Saude Santa Marcelina

🇧🇷

Sao Paulo, Brazil

Tom Baker Cancer Center

🇨🇦

Calgary, Alberta, Canada

Saint John Regional Hospital

🇨🇦

Saint John, New Brunswick, Canada

Cisss de la Monteregie-Centre

🇨🇦

Greenfield Park, Quebec, Canada

CHU de Quebec - Universite Laval

🇨🇦

Quebec City, Quebec, Canada

Ciusss de Lestrie - Centre Hospitalier Universitaire de Sherbrooke (CHUS)

🇨🇦

Sherbrooke, Quebec, Canada

Fundacion Arturo Lopez Perez

🇨🇱

Santiago, Region Metropolitana, Chile

Inmunocel

🇨🇱

Santiago, Region Metropolitana, Chile

Clinica Alemana de Santiago

🇨🇱

Santiago, Region Metropolitana, Chile

Centro Oncologia de Precision Universidad Mayor

🇨🇱

Santiago, Chile

University Hospital Hradec Kralove

🇨🇿

Hradec Kralove, Czechia

University Hospital Kralovske Vinohrady

🇨🇿

Prague, Czechia

Vseobecna Fakultni Nemocnice

🇨🇿

Praha, Czechia

Centre Hospitalier Universitaire (CHU) Rennes

🇫🇷

Rennes, Bretagne, France

Centre Hospitalier Regional Universitaire de Tours

🇫🇷

Tours, Centre Val De Loire, France

Hopital Victor Dupouy Argenteuil

🇫🇷

Argenteuil, Ile De France, France

Gustave Roussy

🇫🇷

Villejuif, Ile De France, France

Nantes University Hospital

🇫🇷

Nantes, Pays De La Loire, France

Hopital de la Conception

🇫🇷

Marseille, Provence-Alpes-Cote d'Azur, France

Centre Hospitalier Universitaire Angers

🇫🇷

Angers, France

Institut Paoli Calmettes

🇫🇷

Marseille, France

Hopital Saint Louis

🇫🇷

Paris, France

Hopital Saint Antoine

🇫🇷

Paris, France

Centre Hospitalier Universitaire (CHU) de Poitiers

🇫🇷

Poitiers, France

Institut de Cancerologie Strasbourg Europe (ICANS)

🇫🇷

Strasbourg, France

University Hospital Wurzburg

🇩🇪

Würzburg, Bavaria, Germany

Kliniken Ostalb Stauferklinikum Schwab Gmund

🇩🇪

Mutlangen, Gmund, Germany

Clinic Frankfurt (Oder)

🇩🇪

Frankfurt, Hesse, Germany

Universitatsmedizin der Johannes-Gutenberg Universitat Mainz

🇩🇪

Mainz, Rheinland-Pfalz, Germany

Hematological Praxis Dresden

🇩🇪

Dresden, Sachsen, Germany

Charite Universitatsmedizin Berlin Campus Benjamin Franklin

🇩🇪

Berlin, Germany

University Hospital Carl Gustav Carus

🇩🇪

Dresden, Germany

Stadtisches Krankenhaus Kiel

🇩🇪

Kiel, Germany

Samson Assuta Ashdod University Hospital

🇮🇱

Ashdod, Israel

Bnai Zion Medical Center

🇮🇱

Haifa, Israel

Hadassah Medical Center

🇮🇱

Jerusalem, Israel

Galilee Medical Center

🇮🇱

Nahariya, Israel

Rabin Medical Center

🇮🇱

Petah-Tikva, Israel

Chaim Sheba Medical Center

🇮🇱

Ramat-Gan, Israel

Tel Aviv Sourasky Medical Center

🇮🇱

Tel Aviv, Israel

Istituto Romagnolo Per Lo Studio Dei Tumori

🇮🇹

Meldola, Forli Cesena, Italy

Irccs Aou Di Bologna- Policlinico Di Sant'Orsola Malpighi

🇮🇹

Bologna, Italia, Italy

IRCCS Ospedale Policlinico San Martino

🇮🇹

Genoa, Liguria, Italy

Candiolo Cancer Institute, FPO, IRCCS

🇮🇹

Candiolo, Torino, Italy

UOC Ematologia e Terapia Cellulare - PO Mazzoni AST Ascoli Piceno

🇮🇹

Ascoli Piceno, Italy

Azienda Ospedaliera Spedali Civili di Brescia

🇮🇹

Brescia, Italy

Istituto Europeo di Oncologia

🇮🇹

Milano, Italy

Federico II University

🇮🇹

Napoli, Italy

AOU Maggiore della Carita-SCDU Ematologia

🇮🇹

Novara, Italy

UO Ematologia Ravenna

🇮🇹

Ravenna, Italy

Santa Maria della Misericordia

🇮🇹

Udine, Italy

Ospedale dell'Angelo - Varese

🇮🇹

Varese, Italy

Center for Hematologic Malignancy

🇰🇷

Goyang, Gyeonggi-do, Korea, Republic of

St. Vincents Hospital - The Catholic University of Korea

🇰🇷

Suwon-si, Gyeonggi-do, Korea, Republic of

Ajou University Hospital

🇰🇷

Suwon-si, Gyeonggi-do, Korea, Republic of

Dong-A University Hospital

🇰🇷

Busan, Korea, Republic of

Pusan National University Hospital

🇰🇷

Busan, Korea, Republic of

Jeonbuk National University Hospital

🇰🇷

Jeonju, Korea, Republic of

Seoul St. Mary's Hospital

🇰🇷

Seoul, Korea, Republic of

Uniwersytecki Szpital Kliniczny

🇵🇱

Wroclaw, Dolnoslaskie, Poland

Uniwersyteckie Centrum Kliniczne

🇵🇱

Gdansk, Pomorskie, Poland

Specjalistyczny Szpital im A. Sokolowskiego w Walbrzychu

🇵🇱

Walbrzych, Lower Silesian, Poland

Pratia MCM Krakow

🇵🇱

Krakow, Malopolska, Poland

Cm Pratia Poznan

🇵🇱

Poznan, Wielkopolska, Poland

Aidport

🇵🇱

Skorzewo, Wielkopolska, Poland

Pratia Onkologia Katowice

🇵🇱

Katowice, Poland

Copernicus Memorial Hospital

🇵🇱

Lodz, Poland

Centrum Innowacyjnych Terapii Samodzielny Publiczny Szpital Kliniczny Nr 4 w Lublinie

🇵🇱

Lublin, Poland

Narodowy Instytut Onkologii im Marii Sklodowskiej Curie Panstwowy Instytut Badawczy Warszawa

🇵🇱

Warszawa, Poland

Hospital Universitario Virgen Macarena

🇪🇸

Sevilla, Andalucia, Spain

Hospital Universitario Central De Asturias

🇪🇸

Oviedo, Asturias, Spain

Son Espases University Hospital

🇪🇸

Palma, Balearic Islands, Spain

Cruces University Hospital (Hospital Universitario Cruces)

🇪🇸

Barakaldo, Bizkaia, Spain

Hospital Universitario Marques de Valdecilla

🇪🇸

Santander, Cantabria, Spain

Complejo Hospitalario Universitario de a Coruna

🇪🇸

A Coruna, Galicia, Spain

Hospital Universitario Quironsalud Madrid

🇪🇸

Pozuelo de Alarcon, Madrid, Spain

Hospital Universitario de Navarra

🇪🇸

Pamplona, Navarra, Spain

University Hospital Vall d'Hebron

🇪🇸

Barcelona, Spain

University Hospital of Santiago de Compostela

🇪🇸

Santiago de Compostela, A Coruna, Spain

Hospital Universitario Virgen De La Victoria Malaga

🇪🇸

Malaga, Andalucia, Spain

Hospital Virgen De Las Nieves De Granada

🇪🇸

Granada, Spain

Chang Gung Medical Foundation Chia Yi Branch

🇨🇳

Chiayi City, Taiwan

Gregorio Maranon

🇪🇸

Madrid, Spain

Clinica Universidad de Navarra

🇪🇸

Madrid, Spain

Fundacion Jimenez Diaz University Hospital

🇪🇸

Madrid, Spain

University Hospital & Research Institute

🇪🇸

Madrid, Spain

Chung-Ho Memorial Hospital

🇨🇳

Kaohsiung, Taiwan

Hospital Universitario HM Sanchinarro, Servicio de Hematologia

🇪🇸

Madrid, Spain

Morales Meseguer Hospital

🇪🇸

Murcia, Spain

Complexo Hospitalario Universitario de Ourense

🇪🇸

Ourense, Spain

Hospital Universitario de Salamanca

🇪🇸

Salamanca, Spain

Hospital Universitario Virgen de Valme

🇪🇸

Sevilla, Spain

University Hospital Virgen del Rocio

🇪🇸

Seville, Spain

Hospital General Universitario de Toledo

🇪🇸

Toledo, Spain

Hospital Clinico Universitario Valencia

🇪🇸

Valencia, Spain

Hospital Universitari and Politecnic La Fe

🇪🇸

Valencia, Spain

Hospital Clinico Lozano Blesa

🇪🇸

Zaragoza, Spain

Kantonsspital Baden

🇨🇭

Baden, Aargau, Switzerland

Cantonal Hospital St Gallen

🇨🇭

St Gallen, Saint Gallen, Switzerland

Kantonsspital Winterthur Medical Oncology

🇨🇭

Winterthur, Schweiz, Switzerland

University Hospital Basel

🇨🇭

Basel, Switzerland

Inselspital Bern University Hospital

🇨🇭

Bern, Switzerland

Chang Gung Memorial Hospital Linkou

🇨🇳

Taoyuan City, Guishan District, Taiwan

Changhua Christian Hospital

🇨🇳

Changhua City, Taiwan

Kaohsiung Chang Gung Memorial Hospital

🇨🇳

Kaohsiung, Taiwan

Taipei Medical University-Shuang Ho Hospital

🇨🇳

New Taipei City, Taiwan

Taichung General Veterans Hospital

🇨🇳

Taichung, Taiwan

National Cheng Kung University Hospital

🇨🇳

Tainan, Taiwan

Tri-Service General Hospital

🇨🇳

Taipei City, Taiwan

National Taiwan University Hospital

🇨🇳

Taipei, Taiwan

Taipei Municipal Wan Fang Hospital

🇨🇳

Taipei, Taiwan

Dr. Abdurrahman Yurtaslan Oncology Training and Research Hospital

🇹🇷

Yenimahalle, Ankara, Turkey

Gazi University

🇹🇷

Ankara, Central Anatolia, Turkey

VM Medical Park Mersin Hospital

🇹🇷

Mezitli, Mersin, Turkey

Tekirdag Namik Kemal University Hospital

🇹🇷

Tekirdag, Suleymanpasa, Turkey

Liv Hospital Ankara

🇹🇷

Ankara, Turkey

VKV American Hopital

🇹🇷

Istanbul, Turkey

Istanbul University Istanbul Faculty of Medicine

🇹🇷

Istanbul, Turkey

Ege University

🇹🇷

Izmir, Turkey

Erci̇yes Uni̇versi̇ty

🇹🇷

Kayseri, Turkey

Sakarya Universty Medical Faculty

🇹🇷

Sakarya, Turkey

Ondokuz Mayis Universitesi Tip Fakultesi Hastanesi

🇹🇷

Samsun, Turkey

Zonguldak Bulent Ecevit University

🇹🇷

Zonguldak, Turkey

Royal Cornwall Hospital NHS Trust

🇬🇧

Truro, Cornwall, United Kingdom

Derriford Hospital and the Royal Eye Infirmary

🇬🇧

Plymouth, Devon, United Kingdom

University Hospitals Dorset

🇬🇧

Bournemouth, Dorset, United Kingdom

Beatson West of Scotland Cancer Centre

🇬🇧

Glasgow, Lanarkshire, United Kingdom

Norfolk and Norwich University Hospital

🇬🇧

Norwich, Norfolk, United Kingdom

Barking, Havering and Redbridge University Hospitals NHS Trust

🇬🇧

Romford, United Kingdom

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