New drug duo aims to slow advanced lung cancer
NCT ID NCT05215340
First seen Jun 27, 2026 · Last updated Aug 20, 2026 · Updated 2 times
Summary
This phase 3 trial tests whether adding the drug Dato-DXd to standard immunotherapy (pembrolizumab) helps people with advanced or metastatic non-small cell lung cancer live longer without their cancer growing. About 740 adults with a high level of a protein called PD-L1 will be randomly assigned to get the combo or pembrolizumab alone. The study compares how long it takes for the cancer to progress and overall survival.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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740 people
The number who actually took part.
- Started
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Mar 2022
- Expected to finish
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Mar 2032
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Participants eligible for inclusion in the study must meet all inclusion criteria within 28 days of randomization into the study. * Sign and date the Tissue Screening and Main Informed Consent Forms, prior to the start of any study-specific qualification procedures. * Adults ≥18 years or the minimum legal adult age (whichever is greater) at the time of informed consent. * Histologically documented non-squamous NSCLC that meets all of the following criteria (Note: Subjects with squamous histology were eligible prior to Protocol Version 5.0. After Protocol Version 5.0, subjects with squamous histology are not eligible. Subjects with mixed histology, including those with a squamous component, remain eligible the study even after Protocol Version 5.0): 1. Stage IIIB or IIIC disease and not candidates for surgical resection or definitive chemoradiation, or Stage IV NSCLC disease at the time of randomization (based on the American Joint Committee on Cancer, Eighth Edition). Participants with early-stage NSCLC who have relapsed should be restaged during screening to ensure their eligibility for the study. 2. Documented negative test results for epidermal growth factor receptor (EGFR), lymphoma kinase (ALK), and proto-oncogene1 (ROS1) actionable genomic alterations (AGAs) based on analysis of tumor tissue. If test results for EGFR, ALK, and ROS1 are not available, subjects are required to undergo testing performed locally for these genomic alterations. 3. No known AGAs in neurotrophic tyrosine receptor kinase (NTRK), proto-oncogene B-raf (BRAF), rearranged during transfection (RET), mesenchymal-epithelial transition factor (MET), or other actionable driver kinases with locally approved therapies in the first-line setting. (Testing for genomic alterations besides EGFR, ALK, and ROS1 is not required prior to randomization). Subjects whose tumors harbor KRAS mutations are eligible for the study. * Has provided a formalin-fixed tumor tissue sample for the measurement of trophoblast cell surface protein 2 (TROP2) protein expression and for the assessment of other exploratory biomarkers. * Tumor has high programmed death receptor-1 (PD-L1) expression (TPS ≥50%) as determined by PD-L1 immunohistochemistry (IHC) 22C3 pharmDx assay by central testing (minimum of 6 slides). * Has an adequate treatment washout period before Cycle 1 Day 1. * Measurable disease based on local imaging assessment using RECIST Version 1.1. * Has left ventricular ejection fraction (LVEF) ≥50% by either an echocardiogram (ECHO) or multigated acquisition scan (MUGA) within 28 days before randomization. * Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1 at screening. * Has a life expectancy of at least 3 months. * Adequate bone marrow function within 7 days before randomization. Exclusion Criteria: * Has received prior systemic treatment for advanced or metastatic NSCLC. * Has received prior treatment for NSCLC with any of the following, including in the adjuvant/neoadjuvant setting: 1. Any agent, including an antibody-drug conjugate, containing a chemotherapeutic agent targeting topoisomerase I. 2. TROP2-targeted therapy. 3. Any anti-programmed death receptor-1 (PD-1), anti-PD-L1, or anti-PD-ligand 2 (L2) agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA-4, OX40, CD137). 4. Any other immune checkpoint inhibitors. Participants who received adjuvant or neoadjuvant therapy OTHER than those listed above, are eligible if the adjuvant/neoadjuvant therapy was completed at least 6 months prior to the diagnosis of advanced/metastatic disease. * Has spinal cord compression or active and untreated central nervous system (CNS) metastases and/or carcinomatous meningitis. Participants with previously treated brain metastases and who are asymptomatic may participate provided they are radiologically stable. * Has received prior radiotherapy \< 4 weeks of start of study intervention or more than 30 Gy (unit of ionizing radiation dose in the International System of Units) to the lung within 6 months of Cycle 1 Day 1. * History of another primary malignancy (beyond NSCLC) except for: 1. Malignancy treated with curative intent and with no known active disease ≥3 years before the first dose of study treatment and of low potential risk for recurrence. 2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease. 3. Adequately treated carcinoma in situ without evidence of disease. 4. Participants with a history of prostate cancer (tumor/node/metastasis stage) of Stage ≤T2cN0M0 without biochemical recurrence or progression and who in the opinion of the Investigator are not deemed to require active intervention. * Has a history of (non-infectious) interstitial lung disease (ILD)/pneumonitis including radiation pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening. * Clinically severe pulmonary compromise, as judged by the investigator, resulting from intercurrent pulmonary illnesses including, but not limited to, any underlying pulmonary disorder, or any autoimmune, connective tissue or inflammatory disorders with pulmonary involvement or prior complete pneumonectomy. * Uncontrolled or significant cardiovascular disease, including: 1. Mean QT interval corrected for heart rate using Fridericia's formula (QTcF) interval \>470 ms regardless of sex (based on the average of the 12-lead electrocardiogram determination at screening). 2. Myocardial infarction within 6 months prior to randomization. 3. Uncontrolled angina pectoris within 6 months prior to randomization. 4. LVEF \<50% by ECHO or MUGA scan within 28 days before randomization. 5. New York Heart Association Class 2 to 4 congestive heart failure (CHF) at screening. 6. Uncontrolled hypertension (resting systolic blood pressure \>180 mmHg or diastolic blood pressure \>110 mmHg) within 28 days before randomization. Participants with a history of Class 2 to 4 CHF prior to screening, must have returned to Class 1 CHF and have LVEF ≥50% (by either an ECHO or MUGA scan within 28 days before randomization) in order to be eligible. * Clinically significant corneal disease. * Has received a live vaccine or live-attenuated vaccine (messenger ribonucleic acid and replication-incompetent adenoviral vaccines are not considered attenuated live vaccines) within 30 days prior to the first dose of study drug. For any participant receiving an approved severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) vaccine, please follow the vaccine label and/or local guidance. * Active, known, or suspected autoimmune disease (has an active autoimmune disease that has required systemic treatment in the past 2 years). * Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosage \>10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy ≤7 days prior to the first dose of study drug. * Has known human immunodeficiency virus (HIV) infection that is not well controlled. * Has an active hepatitis or uncontrolled hepatitis B or active hepatitis C infection. * Has an uncontrolled infection requiring IV antibiotics, antivirals, or antifungals. * Had an allogeneic tissue/solid organ transplant. * Has a history of severe hypersensitivity reactions to either the drug or inactive ingredients (including but not limited to polysorbate 80) of Dato-DXd or pembrolizumab.
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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A.O. Perugia Santa Maria della Misericordia
Perugia, 06132, Italy
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AP-HP - Hopital Tenon
Paris, 75970, France
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APHM - Hopital Nord
Marseille, 13015, France
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AZ Nikolaas
Sint-Niklaas, 9100, Belgium
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Adana Acibadem Hospital
Adana, 1130, Turkey (Türkiye)
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Affiliated Cancer Hospital and Institute of Guangzhou Medical University
Guangzhou, 510095, China
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Akdeniz University Hospital
Antalya, 7070, Turkey (Türkiye)
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American Oncology Partners of Maryland
Bethesda, Maryland, 20817, United States
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Amsterdam Umc, Location Vumc
Amsterdam, 1081 HZ, Netherlands
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Aomori Prefectural Central Hospital
Aomori, Aomori, 030-8553, Japan
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Arizona Oncology NAHOA
Irving, Texas, 75063, United States
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Army Medical Center of PLA
Chongqing, 400042, China
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Asan Medical Center
Songpa-gu, 5505, South Korea
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Asst Sette Laghi Ospedale di Circolo e Fondazione Macchi
Varese, 21100, Italy
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Astera Cancer Care
East Brunswick, New Jersey, 08816, United States
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Austin Hospital
Heidelberg, Victoria, 3084, Australia
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Az Maria Middelares - Campus Maria Middelares
Ghent, 9000, Belgium
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Azienda Ospedaliera dei Colli
Naples, 80131, Italy
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Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
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Bioclinic Thessaloniki
Thessaloniki, 54622, Greece
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Birmingham Heartlands Hospital
Birmingham, B9 5SS, United Kingdom
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Bkmk Hospital
KecskemĂŠt, 6000, Hungary
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Bordeaux University Hospital - Hopital Saint Andre
Bordeaux, 33075, France
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CER SAN JUAN - Centro Polivalente de Asistencia e Investigación Clínica
San Juan, 5400, Argentina
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CHU de Nantes
Nantes, 44093, France
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CHU de Poitier Pole Regional de Cancerologie
Poitiers, 86000, France
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CHUO
Ourense, 32005, Spain
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Cancer Care Center of Brevard
Irving, Texas, 75063, United States
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Cangzhou People's Hospital
Cangzhou, 610001, China
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Centre Hospitalier Universitaire de Lille
Lille, 59000, France
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Centre Hospitalier Universitaire de Montpellier
Montpellier, 34295, France
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Centre Leon Berard
Lyon, 69008, France
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Centro Clinico Champalimau
Lisbon, 1400-038, Portugal
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Centro Hospitalar Universitário de São João
Porto, 4200-319, Portugal
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Centro Hospitalar e Universitário do Porto
Porto, 4099-001, Portugal
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Centro de Estudios Clínicos SAGA
Santiago, Santiago Metropolitan, 7500653, Chile
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Centro de Estudos e Pesquisa de Hematologia e Oncologia - CEPHO
Santo André, 09060-870, Brazil
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Centro de Investigacion Clinica de Oaxaca (CICLO)
Oaxaca City, 68020, Mexico
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Centro de Investigaciones Clinicas Vina Del Mar
Viña del Mar, 254-0488, Chile
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Centro de Investigaciones Medicas y Desarrollo LC S.R.L. (LC Investigacion)
Buenos Aires, Argentina
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Centro de Investigación Pergamino S. A.
Pergamino, 2700, Argentina
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Centrul de Oncologie Sf Nectarie S.R.L.
Craiova, 200542, Romania
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Chang Gung Memorial Hospital Cgmh - Kaohsiung Branch
Kaohsiung City, 833, Taiwan
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Chang Gung Memorial Hospital LinKou
Taoyuan, 333, Taiwan
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Chris Obrien Lifehouse
Camperdown, 2050, Australia
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Chung Shan Medical University Hospital
Taichung, 40201, Taiwan
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Chungbuk National University Hospital
Cheongju-si, North Chungcheong, 28644, South Korea
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Clinica Viedma SA
Viedma, 8500, Argentina
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Clínica de Neoplasias Litoral
Itajaí, 88301-220, Brazil
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Cooperman Barnabas Medical Center
New Brunswick, New Jersey, 08901, United States
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Cryptex Investigacion Clinica Sa de Cv
Cuauhtémoc, 06100, Mexico
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DFCI - South Shore Hospital
South Weymouth, Massachusetts, 02190, United States
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Dana Farber Cancer Institute - Foxborough
Foxborough, Massachusetts, 02035, United States
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Dana-Farber Cancer Institute
Boston, Massachusetts, 02115, United States
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Dartmouth Hitchcock Medical Center
Lebanon, New Hampshire, 03766, United States
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Dokkyo Medical University Hospital
Shimotsuga-gun, Tochigi, 321-0293, Japan
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Dom Lekarski SA
Szczecin, West Pomeranian Voivodeship, 70-784, Poland
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E-Da Hospital
Kaohsiung City, 824, Taiwan
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Ege University
Bornova-İzmir, 35100, Turkey (Türkiye)
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Evangelische Lungenklinik Berlin
Berlin, 13125, Germany
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Faculty of Medicine Chulalongkorn University
Bangkok, 10330, Thailand
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Fejer Megyei Szent Gyorgy Egyetemi Oktato Korhaz
Székesfehérvár, 8000, Hungary
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Fudan University Shanghai Cancer Center
Shanghai Shi, 200032, China
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Fundacion CENIT para la investigación en Neurociencias
Ciudad Autonoma de Buenos Aire, 1125, Argentina
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Fundación Arturo Pérez López
Santiago, 7500921, Chile
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Goztepe Prof. Dr. Suleyman Yalcin City Hospital
Istanbul, 34772, Turkey (Türkiye)
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Grand Hopital de Charleroi - Hopital Saint Joseph
Charleroi, 6000, Belgium
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Guangxi Medical University Affiliated Tumor Hospital
Nanning, Guangxi, 530021, China
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Gyeongsang National University Hospital
Jinju, Gyeongsangnam-do, 52727, South Korea
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Haikou People's Hospital
Haikou, 570208, China
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Harbin Medical University Cancer Hospital
Harbin, 150081, China
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Henan Cancer Hospital
Zhengzhou, Henan, 450008, China
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Hopital FOCH
Suresnes, 92150, France
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Hopital prive du Confluent
Nantes, 44277, France
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Hospital CUF Porto
Porto, 4100-180, Portugal
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Hospital Civil de Guadalajara Fray Antonio Alcalde
Guadalajara, 44280, Mexico
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Hospital Clinic i Provincial de Barcelona
Barcelona, 08036, Spain
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Hospital Clinico San Carlos
Madrid, 28040, Spain
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Hospital Erasto Gaertner
Curitiba, 81520-060, Brazil
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Hospital General Universitario Gregorio Marañon
Madrid, 28007, Spain
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Hospital Privado de la Comunidad
Mar del Plata, B7602CBM, Argentina
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Hospital Regional Universitario Malaga
Málaga, 29010, Spain
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Hospital Universitari Vall D'Hebron
Barcelona, 8035, Spain
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Hospital Universitari i Politècnic La Fe
Valencia, 46026, Spain
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Hospital Universitario Arnau de Vilanova - Lleida
Lleida, 25198, Spain
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Hospital Universitario Dr. Jose Eleuterio Gonzalez
Monterrey, 64460, Mexico
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Hospital Universitario Fundacion Jimenez Diaz
Madrid, 28040, Spain
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Hospital Universitario Miguel Servet
Zaragoza, 50009, Spain
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Hospital Universitario Virgen Macarena
Seville, 41009, Spain
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Hospital Universitario de Valme
Seville, 41014, Spain
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Hubei Cancer Hospital
Wuhan, 430079, China
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Hunan Cancer Hospital
Changsha, 410013, China
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II Klinika Chorob Pluc I Gruzlicy
Bialystok, 15-450, Poland
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IRCCS Istituto Oncologico Giovanni Paolo II
Bari, 70124, Italy
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IRCCS Ospedale San Raffaele
Milan, 20132, Italy
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Ifo Regina Elena
Rome, 144, Italy
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Illinois Cancer Specialists
Irving, Texas, 75063, United States
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Inner Mongolia Medical University- the Affiliated Hospital
Hohhot, 10050, China
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Institut Bergonie
Bordeaux, 33076, France
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Institut Paoli-Calmettes
Marseille, 13273, France
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Instituto Nacional de Câncer - INCA
Rio de Janeiro, 20231-050, Brazil
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Instituto Portuguas de Oncologia do Porto Francisco Gentil
Porto, 4200-072, Portugal
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Instituto de Ensino e Pesquisas Sao Lucas
São Paulo, 01236-030, Brazil
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Instituto de Oncología de Rosario
Rosario, S2000, Argentina
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Instituto de Pesquisas em Saúde - IPS
Caxias do Sul, 95020-972, Brazil
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Instituto do Cancer Brasil - Unidade Taubate
Taubaté, Brazil
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Instytut Centrum Zdrowia Matki Polki
Lodz, Iodzkie, 93-338, Poland
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Irccs Istituto Europeo Di Oncologia
Milan, 20141, Italy
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Ironwood Cancer and Research Center
Chandler, Arizona, 85224, United States
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Jeroen Bosch Ziekenhuis J BZ Hieronymus Bosch Hospital
's-Hertogenbosch, 5223 GZ, Netherlands
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Jiamusi Tumor and Tuberculosis Hospital
Jiamusi, 154007, China
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Jiangsu Province Hospital
Nanjing, 210029, China
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Jilin Cancer Hospital
Changchun, Jilin, 130012, China
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Johns Hopkins University
Baltimore, Maryland, 21205, United States
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Juntendo University Hospital
Bunkyo-ku, Tokyo, 113-8431, Japan
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Kanagawa Cancer Center
Yokohama, Kanagawa, 241-8515, Japan
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Kanazawa University Hospital
Kanazawa, Ishikawa-ken, 920-8641, Japan
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Kansai Medical University Hospital
Hirakata-shi, Osaka, 573-1191, Japan
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Kantonsspital Baden
Baden, 5404, Switzerland
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Kantonsspital Baselland
Liestal, A4410, Switzerland
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Kantonsspital St. Gallen
Sankt Gallen, Switzerland
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Karl-Landsteiner Institute for Lung Research and Pulmonary Oncology c/o Klinik Floridsdorf
Vienna, 1090, Austria
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Klinikum Esslingen GmbH
Esslingen am Neckar, 73730, Germany
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Klinikum Klagenfurt am Wörthersee Abteilung für Lungenkrankheiten
Klagenfurt, Austria
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Klinikum der Universitaet Muenchen
München, 80336, Germany
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Koo Foundation Sun Yat-Sen Cancer Center
Taipei, 112, Taiwan
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Kurume University Hospital
Kurume-shi, Fukuoka, 830-0011, Japan
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Kyungpook National University Chilgok Hospital
Daegu, 42119, South Korea
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Kyushu University Hospital
Fukuoka, Fukuoka, 812-8582, Japan
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Leiden University Medical Center
Leiden, 2333 ZA, Netherlands
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Liaoning Cancer Hospital& Institute
Shenyang, 110801, China
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Linyi Cancer Hospital
Linyi, 276000, China
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LungenClinic Grosshansdorf
Großhansdorf, 22927, Germany
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MS Pneumed Janusz Milanowski, Katarzyna Szmygin-Milanowska Sp. Jawna
Lublin, 20-064, Poland
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Maryland Oncology Hematology
Irving, Texas, 75063, United States
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Matsusaka Municipal Hospital
Matsusaka-shi, Mie-ken, 515-8544, Japan
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McGill University Health Centre
Montreal, H4A 3J2, Canada
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Medical College of Wisconsin
Milwaukee, Wisconsin, 53226, United States
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Medical Park Seyhan Hospital
Seyhan /Adana, 1140, Turkey (Türkiye)
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Memorial Ankara Hospital Ankara
Çankaya, 06520, Turkey (Türkiye)
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Metropolitan Hospital
Neo Faliro, Athens, 14564, Greece
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Metropolitan Hospital
Neo Faliro, 18547, Greece
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Metropolitan Hospital
Piraeus, 18547, Greece
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Montefiore Medical Center
The Bronx, New York, 10461, United States
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NHO Iwakuni Clinical Center
Iwakuni-shi, Yamaguchi, 740-8510, Japan
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NHO Kinki-Chuo Chest Medical Center
Sakai-shi, Osaka, 591-8555, Japan
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NHO Shikoku Cancer Center
Matsuyama, Ehime, 791-0280, Japan
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National Cancer Center
Goyang-si, 10408, South Korea
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National Cancer Center Hospital East
Kashiwa-shi, Chiba, 277-8577, Japan
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National Cheng Kung University Hospital Nckuh
Tainan, 704, Taiwan
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National Hospital Organization Kyushu Cancer Center
Fukuoka, Fukuoka, 811-1395, Japan
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National Taiwan University Hospital
Taipei, 100, Taiwan
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Niigata Cancer Center Hospital
Niigata, Niigata, 961-8566, Japan
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Nottingham University Hospitals
Nottingham, NG5 1PB, United Kingdom
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Onco Clinic Consult SA
Craiova, 200094, Romania
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Oncocenter-Oncologie Clinica SRL
Timișoara, 300166, Romania
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Oncologico Potosino
San Luis Potosí City, 78209, Mexico
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Oncosite - Centro de Pesquisa Clinica Oncologia
Ijuí, 98700-000, Brazil
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Oncovida
Santiago, 7500000, Chile
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Onze-Lieve-Vrouwziekenhuis Olvz - Campus Aalst
Aalst, 9300, Belgium
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Orlandi Oncología
Santiago, 7501010, Chile
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Osaka International Cancer Institute
Osaka, Osaka, 541-8567, Japan
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Osaka Toneyama Medical Center
Osaka, 560-8552, Japan
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Ospedale San Luca
Lucca, 55100, Italy
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PIH Health Whittier Hospital
Whittier, California, 90602, United States
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Peking University Cancer Hospital
Beijing, 100142, China
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Peking University Peoples Hospital
Beijing, 100044, China
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Peninsula and South Eastern Haematology and Oncology Group
Mount Waverley, Victoria, 3149, Australia
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Policlinico Tor Vergata
Rome, 133, Italy
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Prince of Songkla University PSU - Faculty of Medicine
Hat Yai, Changwat Songkhla, 90110, Thailand
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Prince of Wales Hospital / The Chinese University of Hong Kong 99999
Hong Kong, 99999, Hong Kong
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Providence Regional Cancer System
Lacey, Washington, 98503, United States
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Pulmonology Hospital Torokbalint
Törökbálint, 2045, Hungary
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Queen Elizabeth Hospital
Hong Kong, Hong Kong
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Queen Mary Hospital
Pok Fu Lam, 999077, Hong Kong
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Regional Cancer Care Associates LLC
Freehold, New Jersey, 07728, United States
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Ridley-Tree Cancer Center
Santa Barbara, California, 93105, United States
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Rijnstate Ziekenhuis
Arnhem, Gelderland, 6815 AD, Netherlands
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SC Oncomed SRL
Timișoara, 300239, Romania
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Sainte-Catherine Institut du Cancer Avignon-Provence (ICAP)
Avignon, 84000, France
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Saiseikai Kumamoto Hospital
Kumamoto, Kumamoto, 861- 4193, Japan
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Samsung Medical Center
Seoul, 6351, South Korea
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Sanatorio Británico de Rosario
Rosario, S2002, Argentina
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Sanatorio Parque
Rosario, S2001, Argentina
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Santa Casa de Misericordia de Porto Alegre
Porto Alegre, 90050-170, Brazil
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Sc Sigmedical Services Srl
Suceava, 720214, Romania
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Semmelweis University Department of Pulmonology
Budapest, 1083, Hungary
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Sendai Kousei Hospital
Sendai, Miyagi, 980-0873, Japan
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Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do, 13620, South Korea
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Shanghai Pulmonary Hospital
Shanghai, 200433, China
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Sichuan Cancer Hospital
Chengdu, Sichuan, 610049, China
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Siriraj Hospital
Bangkok, 10700, Thailand
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Sotiria General Hosptial of Chest Diseases
Athens, 11527, Greece
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Southern Cancer Center
Irving, Texas, 75063, United States
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Srinagarind Hospital
Muaeng, Changwat Khon Kaen, 40002, Thailand
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St. Luke's Hospital
Thessaloniki, 55236, Greece
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Szpitale Pomorskie Sp. z o.o.
Gdynia, Pomeranian Voivodeship, 81-519, Poland
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Taichung Veterans General Hospital
Taichung, 40705, Taiwan
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Taipei Veterans General Hospital
Taipei, 11217, Taiwan
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Teine Keijinkai Hospital
Sapporo, 006-8555, Japan
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Texas Oncology - Northeast Texas
Irving, Texas, 75063, United States
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Texas Oncology Gulf Coast
Irving, Texas, 75063, United States
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Texas Oncology McAllen
Irving, Texas, 75063, United States
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The Cancer Institute Hospital of JFCR
Kōtoku, Toyko, 135-8550, Japan
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The Catholic Univ. of Korea, Seoul St. Mary'S Hospital
Seoul, 6591, South Korea
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The First Affiliate Hospitalof Xi'An Jiaotong University
Xi'an, 710061, China
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The First Affiliated Hospital Xiamen University
Xiamen, 361001, China
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The First Affiliated Hospital of College of Medicine Zhejiang University
Hanghzou, 310003, China
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The First Affiliated Hospital of Nanchang University
Nanchang, 330006, China
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The First Hospital of China Medical University
Shenyang, 110001, China
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The Oncology Institute of Hope and Innovation
Whittier, California, 90603, United States
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The Queen Elizabeth Hospital
Woodville South, 5011, Australia
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The Second People's Hospital of Neijiang
Neijiang, 641000, China
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The Valley Hospital
Paramus, New Jersey, 07652, United States
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Tianjin Medical University General Hospital
Tianjin, 300052, China
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Toho University Omori Medical Center
Ōta-ku, Toyko, 143-8541, Japan
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Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital
Bunkyō-Ku, Tokyo, 113-8677, Japan
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UCLA HemOnc - Clinical Research Unit
Los Angeles, California, 90095, United States
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UOC Oncologia
Chieti, 66100, Italy
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UPCO - Unidade de Pesquisas Clínicas em Oncologia - Clinica Lacks
Pelotas, 96020-080, Brazil
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Uch-Mhs D/B/A Memorial Health System
Colorado Springs, Colorado, 80909, United States
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Union Hospital Affiliated With Tongji Medical College Huazhong University of Science and Technology
Wuhan, 430022, China
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University Hospital Basel
Basel, 4031, Switzerland
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University Hospital Kyoto Prefectural University of Medicine
Kyoto, 602-8566, Japan
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University Hospital of Ioannina Uhi
Ioannina, 45500, Greece
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University of Texas Health Science Center San Antonio
San Antonio, Texas, 78229, United States
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Utah Cancer Specialists
Salt Lake City, Utah, 84106, United States
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VA Puget Sound Health Care System - VAPSHCS
Seattle, Washington, 98108, United States
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Veszprem Megyei Tudogyogyintezet Farkasgyepu
Farkasgyepű, 8582, Hungary
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Xiangyang Central Hospital- 5 Lumen Avenue
Xiangyang, 441000, China
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Xinjiang Tumor Hospital
Ürümqi, 830000, China
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Yamaguchi-Ube Medical Center
Ube-shi, Yamaguchi, 755-0241, Japan
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Yamanashi Prefectural Central Hospital
Kofu, Japan
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Yunnan Cancer Hospital
Kunming, 650118, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can radiation turn tumors into targets for immunotherapy?
- Seeing the fight: new imaging tracer may reveal how immune cells attack lung cancer
- Can a pill outperform chemo for a Hard-to-Treat lung cancer mutation?
- Can a new drug shrink Hard-to-Treat tumors?
- Breath test may reveal who benefits from lung cancer immunotherapy
- Targeted radiation and immunotherapy join forces against Hard-to-Treat lung cancer