A Trial to See if the Combination of Fianlimab With Cemiplimab Works Better Than Pembrolizumab for Preventing or Delaying Melanoma From Coming Back After it Has Been Removed With Surgery
- Conditions
- Melanoma
- Interventions
- Registration Number
- NCT05608291
- Lead Sponsor
- Regeneron Pharmaceuticals
- Brief Summary
This study is researching an experimental drug called REGN3767, also known as fianlimab (R3767), when combined with another medication called cemiplimab (each individually called a "study drug" or called "study drugs" when combined) compared with an approved medication called pembrolizumab.
The objective of this study is to see if the combination of fianlimab and cemiplimab is an effective treatment compared to pembrolizumab in patients that have had melanoma removal surgery but are still at high risk for the recurrence of the disease. Pembrolizumab is an approved treatment in some countries in this clinical setting.
The study is looking at several other research questions, including:
* What side effects may happen from receiving the study drugs.
* How much study drug is in the blood at different times.
* Whether the body makes antibodies against the study drug (which could make the drug less effective or could lead to side effects). Antibodies are proteins that are naturally found in the blood stream that fight infections.
* How administering the study drugs might improve quality of life.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 1564
- All patients must be either stage IIB, IIC, III, or stage IV per American Joint Committee on Cancer (AJCC) 8th edition and have histologically confirmed melanoma that is completely surgically resected in order to be eligible as defined by the protocol
- Complete surgical resection must be performed within 12 weeks prior to randomization, and enrollment may occur only after satisfactory wound healing from the surgery
- All patients must have disease-free status documented by a complete physical examination and imaging studies within 4 weeks prior to randomization, as described in the protocol
Key
- Uveal melanoma
- Any evidence of residual disease after surgery by imaging, pathology, or cytology.
- Ongoing or recent (within 2 years) evidence of clinically significant autoimmune disease that required treatment
- Uncontrolled infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C (HCV) infection; or diagnosis of immunodeficiency that is related to, or results in chronic infection, as described in the protocol
- Another malignancy that is currently progressing or that required active treatment in the past 5 years, as described in the protocol
- Participants with a history of myocarditis
- Adolescent patients (≥12 to <18 years old) with body weight <40 kg
Note: Other Protocol Defined Inclusion/ Exclusion Criteria Apply
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Fianlimab HD + Cemiplimab Fianlimab Patients will be administered one combination dose of fianlimab high dose (HD) and cemiplimab Fianlimab HD + Cemiplimab Cemiplimab Patients will be administered one combination dose of fianlimab high dose (HD) and cemiplimab Fianlimab LD + Cemiplimab Fianlimab Patients will be administered one combination dose of fianlimab low dose (LD) and cemiplimab Fianlimab LD + Cemiplimab Cemiplimab Patients will be administered one combination dose of fianlimab low dose (LD) and cemiplimab Pembrolizumab Pembrolizumab Patients will be administered one dose of pembrolizumab co-infused with saline/dextrose placebo Pembrolizumab Placebo Patients will be administered one dose of pembrolizumab co-infused with saline/dextrose placebo
- Primary Outcome Measures
Name Time Method Relapse free survival (RSF) Up to 5 Years Time from randomization to the first documented recurrence of disease at any site (excluding new primary melanomas) or death from any cause, whichever occurs first.
- Secondary Outcome Measures
Name Time Method Distant metastasis-free survival (DMFS) Up to 5 Years Time between the date of randomization and the date of the first distant metastasis.
Occurrence of immune-mediated EAEs (im-EAEs) Up to 5 Years imAEs are a unique set of toxicities thought to be caused by unrestrained cellular immune responses.
Overall survival (OS) Up to 5 Years Time from randomization to the date of death.
Occurrence of treatment-emergent adverse events (TEAEs) Up to 5 Years A TEAE is any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product, which does not necessarily have a causal relationship with this treatment.
Occurrence of serious adverse events (SAEs) Up to 5 Years An SAE is any untoward medical occurrence that at any dose:
* Results in death - includes all deaths, even those that appear to be completely unrelated to study drug (eg, a car accident in which a patient is a passenger).
* Is life-threatening
* Requires in-patient hospitalization or prolongation of existing hospitalization.
* Results in persistent or significant disability/incapacity
* Is a congenital anomaly/birth defect.
* Is an important medical eventOccurrence of adverse events of special interest (AESIs) Up to 5 Years An AESI (serious or non-serious) is one of scientific and medical concern specific to the sponsor's product or program, for which ongoing monitoring and rapid communication by the Investigator to the sponsor can be appropriate. Such an event might warrant further investigation in order to characterize and understand it
Occurrence of laboratory abnormalities Up to 5 Years As assessed by the NCI-CTCAE grading system (≥ Grade 3 or higher)
Concentrations of fianlimab in serum over time Up to 5 Years The concentrations of fianlimab over time will be summarized by descriptive statistics by study arm for the overall population and for adolescent patients.
Patient report outcomes (PRO) for adults as measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30 (EORTC-QLQ-C30) Up to 5 Year The EORTC QLQ-C30 (Version 3) uses for the questions 1 to 28 a 4-point scale. The scale scores from 1 to 4: 1 ("Not at all"), 2 ("A little"), 3 ("Quite a bit") and 4 ("Very much"). Half points are not allowed. The range is 3. For the raw score, less points are considered to have a better outcome.
The EORTC QLQ-C30 (Version 3) uses for the questions 29 and 30 a 7-points scale. The scale scores from 1 to 7: 1 ("very poor") to 7 ("excellent"). Half points are not allowed. The range is 6. More points are considered to have a better outcome.PRO for adults as measured by the European Quality of Life Dimension 5 (EQ-5D-5L) Up to 5 Years The EQ-5D-5L a descriptive system that comprises five 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 patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.
PRO for adults as determined by the Patient Global Impressions Scale (PGIS) Up to 5 Years The PGIS is a single 1-item questionnaire designed to assess participant's overall impression of disease severity at a given point in time by using a 4-point Likert scale that ranges from (1) = "none (no symptoms)" to (4) = "severe".
Time to physical functioning deterioration per EORTC QLQ-C30 Up to 5 Years Occurrence of TEAEs resulting in death Up to 5 Years A TEAE resulting in death is any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product, which does not necessarily have a causal relationship with this treatment.
Occurrence of dose-limiting toxicity (DLT) Up to 5 Years A DLT is defined as a study-drug related TEAE, including imAEs, that could preclude enrolling additional adolescent patients at the selected dose. Dose-limiting toxicity will be evaluated in adolescents only.
Occurrence of interruption or discontinuation of study drug(s) due to TEAE Up to 5 Years A TEAE is any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product, which does not necessarily have a causal relationship with this treatment.
Concentrations of cemiplimab in serum over time Up to 5 Years The concentrations of cemiplimab over time will be summarized by descriptive statistics by study arm for the overall population and for adolescent patients.
Concentration of finalimab anti-drug antibodies (ADA) and neutralizing antibodies Up to 5 Years Immunogenicity will be characterized per drug molecule by ADA and NAb status.
Concentration of cemiplimab anti-drug antibodies (ADA) and neutralizing antibodies Up to 5 Years Immunogenicity will be characterized per drug molecule by ADA and NAb status.
PRO for adults as determined by the Patient Global Impressions of Change Scale (PGIC) Up to 5 Years The PGIC is a single-item questionnaire designed to assess the participant's overall sense of whether there has been a change since starting treatment as rated on a 5-point Likert scale anchored by (1) "much better" to (5) "much worse", with (4) = "no change".
Time to global health status/quality of life deterioration per EORTC QLQ-C30 Up to 5 years PRO for adults as measured by the Functional Assessment of Cancer Therapy (FACT) - melanoma Up to 5 Years The FACT-M is a melanoma-specific quality of life questionnaire that is composed of items from the Functional Assessment of Cancer Therapy-General (FACT-G). The FACT-M is scored on a 5 point Likert-scale: "Not at all", "A little bit", "Somewhat", "Quite a bit", and "Very much.". A Higher score represents higher Health Related Quality of Life (HRQoL).
Time to role functioning deterioration per EORTC QLQ-C30 Up to 5 Years
Trial Locations
- Locations (211)
Sainte Catherine Institut du Cancer Avignon Provence
🇫🇷Avignon, France
N_Hôpital Ambroise-Paré
🇫🇷Boulogne Billancourt, France
CHU Estaing
🇫🇷Clermont Ferrand, France
Incliva - Instituto de Investigacion Sanitaria
🇪🇸Valencia, Spain
Baskent University
🇹🇷Yuregir, Adana, Turkey
Dicle University - Medical Faculty Campus
🇹🇷Sur, Diyarbakir, Turkey
Kocaeli University
🇹🇷İzmit, Kocaeli, Turkey
BioClinic Thessaloniki
🇬🇷Thessaloniki, Greece
Interbalkan Medical Center
🇬🇷Thessaloniki, Greece
UCK
🇵🇱Gdansk, Pomerania, Poland
Instituto Valenciano de Oncologia
🇪🇸Valencia, Spain
UC San Diego
🇺🇸La Jolla, California, United States
UCSF Medical Center at Mission Bay
🇺🇸San Francisco, California, United States
John Wayne Cancer Institute (JWCI)
🇺🇸Santa Monica, California, United States
The Melanoma And Skin Cancer Institute
🇺🇸Englewood, Colorado, United States
Miami Cancer Institute at Baptist Health, Inc.
🇺🇸Miami, Florida, United States
Orlando Health
🇺🇸Orlando, Florida, United States
Moffitt Cancer Center
🇺🇸Tampa, Florida, United States
Northwestern University
🇺🇸Chicago, Illinois, United States
Massachusetts General Hospital
🇺🇸Boston, Massachusetts, United States
Dana-Farber Cancer Institute
🇺🇸Boston, Massachusetts, United States
Karmanos Cancer Institute
🇺🇸Detroit, Michigan, United States
Rutgers Cancer Institute of New Jersey
🇺🇸New Brunswick, New Jersey, United States
Laura & Isaac Perlmutter Cancer Center at NYU Langone Health
🇺🇸New York, New York, United States
Columbia University
🇺🇸New York, New York, United States
University of Rochester
🇺🇸Rochester, New York, United States
Lineberger Comprehensive Cancer Center
🇺🇸Chapel Hill, North Carolina, United States
Duke Cancer Institute, University Hospital
🇺🇸Durham, North Carolina, United States
University Hospitals Cleveland Medical Center
🇺🇸Cleveland, Ohio, United States
Cleveland Clinic Foundation
🇺🇸Cleveland, Ohio, United States
The Ohio State University James Comprehensive Cancer Center
🇺🇸Columbus, Ohio, United States
St Lukes University Health Network
🇺🇸Easton, Pennsylvania, United States
University Of Pittsburgh
🇺🇸Pittsburgh, Pennsylvania, United States
University of Tennessee Medical Center
🇺🇸Knoxville, Tennessee, United States
Tennessee Oncology - Centennial Clinic Location
🇺🇸Nashville, Tennessee, United States
Verdi Oncology
🇺🇸Nashville, Tennessee, United States
UT Southwestern Medical Center
🇺🇸Dallas, Texas, United States
Intermountain Medical Center
🇺🇸Murray, Utah, United States
University of Virginia Medical Center
🇺🇸Charlottesville, Virginia, United States
Fundacion Centro de Investigaciones para la Transformacion (CENIT)
🇦🇷Caba, Buenos Aires, Argentina
Centro de Investigacion Pergamino
🇦🇷Pergamino, Buenos Aires, Argentina
Clinica Viedma S.A.
🇦🇷Viedma, Rio Negro, Argentina
Instituto de Oncologia de Rosario
🇦🇷Rosario, Santa Fe, Argentina
Centro Medico San Roque
🇦🇷San Miguel de Tucuman, Tucuman, Argentina
DIABAID - Instituto de Asistencia Integral en Diabetes
🇦🇷Caba, Argentina
Blacktown Cancer and Haematology Centre - Blacktown Hospital
🇦🇺Blacktown, New South Wales, Australia
Lismore Base Hospital
🇦🇺Lismore, New South Wales, Australia
Liverpool Hospital - Cancer Therapy Centre
🇦🇺Liverpool, New South Wales, Australia
Melanoma Institute of Australia
🇦🇺Wollstonecraft, New South Wales, Australia
Flinders Medical Centre
🇦🇺Bedford Park, South Australia, Australia
Calvary North Adelaide Hospital
🇦🇺North Adelaide, South Australia, Australia
Eastern Health
🇦🇺Box Hill, Victoria, Australia
Andrew Love Cancer Centre
🇦🇺Geelong, Victoria, Australia
Alfred Hospital
🇦🇺Melbourne, Victoria, Australia
One Clinical Research at Hollywood Private Hospital
🇦🇺Nedlands, Western Australia, Australia
Vitaz campus Sint-Niklaas Moerland
🇧🇪Sint-Niklaas, Oost-Vlaanderen, Belgium
AZ Groeninge
🇧🇪Kortrijk, West-Vlaanderen, Belgium
LTD New Hospitals
🇬🇪Tbilisi, Georgia
Cliniques Universitaires Saint-Luc
🇧🇪Bruxelles, Belgium
Hospital das Clinicas da Universidade Federal de Minas Gerais
🇧🇷Belo Horizonte, Minas Gerais, Brazil
Liga Paranaense de Combate ao Cancer - Hospital Erasto Gaertner
🇧🇷Curitiba, Parana, Brazil
INCA Instituto Nacional de Cancer
🇧🇷Santo Cristo, Rio De Janeiro, Brazil
Oncosite Centro De Pesquisa Em Oncologia
🇧🇷Ijui, Rio Grande Do Sul, Brazil
Instituto do Cancer em Hospital Sao Vicente de Paulo
🇧🇷Passo Fundo, Rio Grande Do Sul, Brazil
Hospital de Clinicas de Porto Alegre
🇧🇷Porto Alegre, Rio Grande Do Sul, Brazil
Hospital Moinhos de vento
🇧🇷Porto Alegre, Rio Grande Do Sul, Brazil
Centro de Pesquisa em Oncologia PUCRS
🇧🇷Porto Alegre, Rio Grande Do Sul, Brazil
Catarina Pesquisa Clinica
🇧🇷Itajai, Santa Catarina, Brazil
Instituto Joinvilense de Hematologia e Oncologia
🇧🇷Joinville, Santa Catarina, Brazil
Animi Unidade de Tratamento Oncologico
🇧🇷Lages, Santa Catarina, Brazil
Fundacao Pio XII - Hospital de Amor
🇧🇷Barretos, Sao Paulo, Brazil
Fundacao Faculdade Regional de Medicina de Sao Jose do Rio Preto - Hospital de Base
🇧🇷Sao Jose do Rio Preto, Sao Paulo, Brazil
Unimed Sorocaba
🇧🇷Sorocaba, Sao Paulo, Brazil
Instituto COI
🇧🇷Rio de Janeiro, Brazil
Hemomed
🇧🇷Sao Paulo, Brazil
Hospital Sirio Libanes
🇧🇷Sao Paulo, Brazil
Sao Camilo Oncologia
🇧🇷Sao Paulo, Brazil
Dr. Everett Chalmers Hospital
🇨🇦Fredericton, New Brunswick, Canada
Royal Victoria Regional Health Centre
🇨🇦Barrie, Ontario, Canada
Sunnybrook Health Sciences Centre
🇨🇦Toronto, Ontario, Canada
Princess Margaret Cancer Centre
🇨🇦Toronto, Ontario, Canada
Clinica UC San Carlos de Apoquindo
🇨🇱Santiago, Region Metropolitana, Chile
Centro Oncologia de Precision Universidad Mayor
🇨🇱Santiago, Region Metropolitana, Chile
Oncocentro APYS
🇨🇱Vina del Mar, Valparaiso, Chile
Masaryk Memorial Cancer Institute
🇨🇿Brno, Brno Mesto, Czechia
University Hospital Hradec Kralove
🇨🇿Hradec Kralove, North Central Czech Republic, Czechia
University Hospital Ostrava
🇨🇿Ostrava, Czechia
Centre Georges Francois Leclerc
🇫🇷Dijon, Bourgogne, France
CHU-Dijon
🇫🇷Dijon, Burgundy, France
Besancon Regional University Hospital Center
🇫🇷Besancon, Doubs, France
Chu De Bordeaux
🇫🇷Bordeaux, Gironde, France
Institut Claudius Regaud, IUCT-Oncopole
🇫🇷Toulouse, Haute-Garonne, France
CHU de Lille
🇫🇷Lille, Hauts-de-France, France
Service de Dermatologie CHU Saint Eloi
🇫🇷Montpellier Cedex 5, Herault, France
Hopital Avicenne
🇫🇷Bobigny, Ile De France, France
Hospital Henri Mondor
🇫🇷Creteil, Ile De France, France
Saint Louis Hospital
🇫🇷Paris, Ile De France, France
Centre Hospitalier Universitaire Grenoble Alpes
🇫🇷La Tronche, Isere, France
Centre Francois Baclesse (CFB)
🇫🇷Caen, Normandy, France
Centre Hospitalier Le Mans
🇫🇷Le Mans, Pays De La Loire, France
Nantes University Hospital
🇫🇷Nantes, Pays De La Loire, France
CHU Amiens-Picardie
🇫🇷Amiens, Picardie, France
Centre Hospitalier Universitaire De Nice Hopital De L Archet
🇫🇷Nice, France
Centre Hospitalier de Valence
🇫🇷Valence, France
Institut Gustave Roussy
🇫🇷Villejuif, France
Tbilisi State Medical University and Ingorokva High Medical Technology University Clinic
🇬🇪Tbilisi, Caucasus, Georgia
Cancer Center of Adjara
🇬🇪Batumi, Georgia
Acad.Fridon Todua Medical Center- Research Institute of Clinical Medicine
🇬🇪Tbilisi, Georgia
Israeli Georgian Medical Research Clinic Helsicore
🇬🇪Tbilisi, Georgia
JSC K. Eristavi National Center of Experimental and Clinical Surgery
🇬🇪Tbilisi, Georgia
TIM - Tbilisi Institute of Medicine
🇬🇪Tbilisi, Georgia
University Medical Center Mannheim
🇩🇪Mannheim, Baden Wurttemberg, Germany
University of Tuebingen
🇩🇪Tuebingen, Baden Wurttemberg, Germany
University Hospital Augsburg
🇩🇪Augsburg, Bavaria, Germany
Dermatology Erlangen
🇩🇪Erlangen, Bavaria, Germany
University Hospital of Regensburg
🇩🇪Regensburg, Bavaria, Germany
LMU Klinikum
🇩🇪Munich, Bayern, Germany
Klinikum Darmstadt GmbH
🇩🇪Darmstadt, Hessen, Germany
University Clinic Frankfurt
🇩🇪Frankfurt, Hessen, Germany
University Medical Center Goettingen
🇩🇪Gottingen, Lower Saxony, Germany
Helios Kliniken Schwerin
🇩🇪Schwerin, Mecklenburg / Vorpommern, Germany
University Hospital Muenster
🇩🇪Munster, North Rhine Westphalia, Germany
Universitatsklinikum Essen
🇩🇪Essen, North Rhine-Westphalia, Germany
Fachklinik Hornheide
🇩🇪Muenster, North Rhine-Westphalia, Germany
Ruhr University Bochum
🇩🇪Bochum, Northrhine Westphalia, Germany
Hautklinik
🇩🇪Ludwigshafen, Rheinland-Pfalz, Germany
Skin Cancer Center Harz
🇩🇪Quedlinburg, Saxony-Anhalt, Germany
University Hospital Dresden
🇩🇪Dresden, Saxony, Germany
University Hospital of Universitatsklinikum Schleswig Holstein (UKSH) Campus Kiel
🇩🇪Kiel, Schleswig Holstein, Germany
Universitatsklinikum Schleswig Holstein Campus Luebeck
🇩🇪Luebeck, Schleswig Holstein, Germany
Helios Klinikum Erfurt
🇩🇪Erfurt, Thuringia, Germany
Charite Universitaetsmedizin Berlin
🇩🇪Berlin, Germany
Klinikum Bremen Ost
🇩🇪Bremen, Germany
National and Kapodistrian University of Athens
🇬🇷Athens, Attica, Greece
Metropolitan Hospital
🇬🇷Neo Faliro, Attica, Greece
Ongology Theageneio Thessaloniki
🇬🇷Thessaloniki, Greece
Galway University Hospital
🇮🇪Galway, Connacht, Ireland
Cork University Hospital
🇮🇪Cork, Ireland
Beaumont Hospital
🇮🇪Dublin, Ireland
St Vincents University Hospital
🇮🇪Dublin, Ireland
Haemek Medical Center
🇮🇱Afula, Northern District, Israel
Hadassah Medical Organization
🇮🇱Jerusalem, Israel
Sheba Medical Center
🇮🇱Tel Hashomer, Israel
Clinica Oncologica, AOU Riuniti Ancona
🇮🇹Ancona, An, Italy
U.O.C. Oncologia Medica ed Ematologia (U.O.C Medical Oncology and Hematology)
🇮🇹Naples, Campania, Italy
Istituto Romagnolo per lo Studio dei Tumori (IRST)
🇮🇹Meldola, Forli Cesena, Italy
Istituto Clinico Humanitas
🇮🇹Milan, Lombardy, Italy
Istituto dei Tumori
🇮🇹Bari, Italy
Azienda Ospedaliera Santa Croce i Carle
🇮🇹Cuneo, Italy
Istituto Europeo di Oncologia
🇮🇹Milano, Italy
Instituto Nazionale Tumori Fondazione Giovanni Pascale
🇮🇹Naples, Italy
University of Perugia
🇮🇹Perugia, Italy
Fondazione Policlinico Universitrio a. Gemelli - IRCCS
🇮🇹Rome, Italy
Campus Bio-Medico di Roma
🇮🇹Rome, Italy
Istituto Dermopatico dell'Immacolata
🇮🇹Rome, Italy
Santa Chiara Hospital
🇮🇹Trento, Italy
Azienda Sanitaria Universitaria del Friuli Centrale
🇮🇹Udine, Italy
Preparaciones Oncologica SC
🇲🇽Leon, Guanajuato, Mexico
Antiguo Hospital Civil de Guadalajara Fray Antonio Alcalde
🇲🇽Guadalajara, Jalisco, Mexico
Pan American Clinical Research
🇲🇽Guadalajara, Jalisco, Mexico
iCan Oncology
🇲🇽Monterrey, Nuevo Leon, Mexico
Neurociencias Estudios Clinicos SC
🇲🇽Culiacan, Sinaloa, Mexico
Centro De Atencion E Investigacion Clinica En Oncologia SCP
🇲🇽Merida, Yucatan, Mexico
Faicic Centro de Investigacion Clinica de Veracruz
🇲🇽Veracruz, Mexico
Mazowiecki Szpital Wojewodzki, Siedleckie Centrum Onkologii
🇵🇱Siedlce, Mazxowieckie, Poland
Copernicus Podmiot Leczniczy Sp. z o.o.Wojewodzie Centrum Onkologii
🇵🇱Gdansk, Pomorskie, Poland
Wojewodzki Szpital Specjalistyczny im. Janusza Korczaka w Słupsku Sp. z o.o.
🇵🇱Slupsk, Pomorskie, Poland
Poznan University of Meidcla Science
🇵🇱Poznan, Wielkopolska, Poland
Institute of Oncology Bucharest
🇷🇴Bucharest, Bucuresti, Romania
Radiotherapy Center Cluj
🇷🇴Floresti, Cluj County, Romania
Cardiomed
🇷🇴Cluj-Napoca, Cluj, Romania
Institute of Oncology Prof. Dr Ion Chirircuta
🇷🇴Cluj-Napoca, Cluj, Romania
Sfantul Nectarie Oncology Center
🇷🇴Craiova, Dolj, Romania
Oncocenter Oncologie Clinica S.R.L
🇷🇴Timisoara, Timis, Romania
Oncomed
🇷🇴Timisoara, Timis, Romania
Centrul De Oncologie Euroclinic
🇷🇴Iasi, Romania
The Medical Oncology Centre of Rosebank
🇿🇦Johannesburg, Gauteng, South Africa
Wilgers Oncology Centre
🇿🇦Pretoria, Gauteng, South Africa
Groote Schuur Hospital
🇿🇦Cape Town, Western Cape, South Africa
Cape Town Oncology Trials
🇿🇦Kraaifontein, Western Cape, South Africa
Hospital Universitario Central De Asturias
🇪🇸Oviedo, Asturias, Spain
H. Germans Trias i Pujol, ICO-Badalona
🇪🇸Badalona, Barcelona, Spain
Hospital Universitario Marques de Valdecilla
🇪🇸Santander, Cantabria, Spain
Instituto Oncologico Dr Rosell Hospital Universitari Quiron Dexeus Location
🇪🇸Barcelona, Catalunya, Spain
Hospital Vall d'Hebron
🇪🇸Barcelona, Spain
Hospital Clinic de Barcelona
🇪🇸Barcelona, Spain
Catalan Institute of Oncology (ICO) Hospitalet
🇪🇸Barcelona, Spain
Hospital Universitario Virgen de las Nieves
🇪🇸Granada, Spain
Hospital Universitario Lucus Augusti
🇪🇸Lugo, Spain
Hospital General Universitario Gregorio Maranon
🇪🇸Madrid, Spain
Hospital Universitario 12 de Octubre Universidad Complutense de Madrid UCM
🇪🇸Madrid, Spain
Hospital Universitario La Pa<
🇪🇸Madrid, Spain
Centro Integral Oncologico HM Clara Campal
🇪🇸Madrid, Spain
Hospital Universitario Virgen Macarena
🇪🇸Seville, Spain
Gaziantep Medicalpoint Hospital
🇹🇷Gaziantep, Sehitkamil, Turkey
Gulhane Research And Training Hospital
🇹🇷Ankara, Turkey
Ozel Liv Hospital
🇹🇷Ankara, Turkey
Sbu Doctor Abdurrahman Yurtaslan Ankara Onkoloji Suam
🇹🇷Ankara, Turkey
Memorial Ankara Hospital
🇹🇷Ankara, Turkey
Trakya University
🇹🇷Edirne, Turkey
Istanbul University Cerrahpasa at Cerrahpasa Medical Faculty
🇹🇷Istanbul, Turkey
Istanbul Medeniyet University - Prof Dr Suleyman Yalcin Sehir Hospital
🇹🇷Istanbul, Turkey
Royal Devon and Exeter Hospital NHS Trust
🇬🇧Exeter, Devon, United Kingdom
Edinburgh Cancer Centre
🇬🇧Edinburgh, Lothian, United Kingdom
Bristol Haematology And Oncology Centre (BHOC) - Bristol Cancer Institute
🇬🇧Bristol, Somerset, United Kingdom
The Royal Marsden NHS Foundation Trust
🇬🇧Sutton, Surrey, United Kingdom
University Hospital Coventry and Warwickshire Nhs Trust
🇬🇧Coventry, West Midlands, United Kingdom
Saint Bartholomew's Hospital
🇬🇧London, United Kingdom
University College London Hospitals
🇬🇧London, United Kingdom
The Christie
🇬🇧Manchester, United Kingdom
Taunton and Somerset NHS Foundation Trust
🇬🇧Taunton, United Kingdom