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JOURNAL ONKOLOGIE – STUDIE
STAR-121

Zimberelimab and Domvanalimab in Combination With Chemotherapy Versus Pembrolizumab With Chemotherapy in Patients With Untreated Metastatic Non-Small Cell Lung Cancer

Rekrutierend

NCT-Nummer:
NCT05502237

Studienbeginn:
Oktober 2022

Letztes Update:
08.04.2024

Wirkstoff:
zimberelimab, Domvanalimab, Pembrolizumab, Carboplatin, Cisplatin, Paclitaxel, Nab-Paclitaxel, Pemetrexed

Indikation (Clinical Trials):
Lung Neoplasms, Carcinoma, Non-Small-Cell Lung

Geschlecht:
Alle

Altersgruppe:
Erwachsene (18+)

Phase:
Phase 3

Sponsor:
Gilead Sciences

Collaborator:
Arcus Biosciences, Inc.

Studienleiter

Gilead Study Director
Study Director
Gilead Sciences

Kontakt

Gilead Clinical Study Information Center
Kontakt:
Phone: 1-833-445-3230 (GILEAD-0)
E-Mail: GileadClinicalTrials@gilead.com
» Kontaktdaten anzeigen

Studienlocations
(3 von 202)

Augusta-Kranken-Anstalt gGmbh Klinik für Hämatologie Onkologie und Palliativmedizin
44791 Bochum
(Nordrhein-Westfalen)
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Klinikum Chemnitz gGmbH
9116 Chemnitz
(Sachsen)
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Universitatsklinikum Essen / Westdeutsches Tumorzentrum, Innere Klinik (Tumorforschung)
45122 Essen
(Nordrhein-Westfalen)
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Universitätsklinikum Freiburg, Klinik für Innere Medizin I Hämatologie, Onkologie und Stammzelltransplantation
79106 Freiburg
(Baden-Württemberg)
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LungenClinic Grosshansdorf
22927 Grosshansdorf
(Schleswig-Holstein)
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Krankenhaus Martha-Maria Halle Dölau
06120 Halle
(Sachsen-Anhalt)
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Asklepios Kliniken Hamburg
21075 Hamburg
(Hamburg)
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Katholisches Marienkrankenhaus gGmbH
22087 Hamburg
(Hamburg)
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Lungenklinik Hemer, Zentrum fur Pneumologie and Thoraxchirurgie
58675 Hemer
(Nordrhein-Westfalen)
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Vincentius-Diakonissen-Kliniken gAG, St. Vincentius-Kliniken, Medizinische Klinik 2
76137 Karlsruhe
(Baden-Württemberg)
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IBZ - Interdisziplinäres Brustzentrum am Klinikum Kassel
Mönchebergstraße 41-43
34125 Kassel
(Hessen)
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Kliniken der Stadt Köln ggmbh, Krankenhaus Koln-Merheim/Lungenklinik
51109 Köln
(Nordrhein-Westfalen)
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Universitatsklinikum Schleswig-Holstein
23538 Lubeck
(Schleswig-Holstein)
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Johannes Wesling Klinikum Minden
32429 Minden
(Nordrhein-Westfalen)
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Munchen Klinik Bogenhausen, Klinik fur Pneumologie und Pneumologische Onkologie
81925 Munchen
(Bayern)
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Palo Verde Hematology Oncology Ltd
85304 Glendale
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California Cancer Associates for Research and Excellence
92069 San Marcos
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Innovative Clinical Research Institute
90606 Whittier
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Eastern CT Hematology and Oncology Associates
06360 Norwich
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Lake City Cancer Care
32024 Lake City
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Florida Cancer Specialists
34232 Sarasota
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Peachtree Hematology Oncology Consultants
30318 Atlanta
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Messino Cancer Centers
28806 Asheville
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Oncology Hematology Care, Inc.
45242 Cincinnati
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Hematology & Oncology Associates
97401 Eugene
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AHN Allegheny General Hospital
15212 Pittsburgh
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Arlington Cancer Center
76012 Arlington
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Texas Oncology - Austin
78745 Austin
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Texas Oncology- Denison
75090 Sherman
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US Oncology Investigational Products Center (IPC)
22205 Arlington
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Oncology and Hematology Associates of Southwest Virginia, Inc
24060 Blacksburg
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Northwest Cancer Specialists, PC
98684 Vancouver
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Investigaciones CORI S.R.L.
F5300COE Capital
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Centro Médico Privado Centro de Especialidades Médicas Ambulatorias e Investigación Clínica
X5008HHW Cardoba
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Centro Medico Barrio Parque
1426 Ciudad Autanoma Buenos Aires
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Sanatorio Britanico de Rosario
2000 Rosario
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S2000DSV Rosario
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S2002KDS Rosario
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Instituto Medico de la Fundacion Estudios Clinicos
S2013DTC Rosario
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CAIPO - Centro para la Atención Integral del Paciente Oncológico
4000 San Miguel de Tucumán
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Klinikum Klagenfurt am Woerthersee
Klagenfurt Am Woerthersee
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Ordensklinikum Linz GmbH, Elisabethinen
4020 Linz
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Krankenhaus Nord - Klinik Floridsdorf
A-1140 Wien
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Grand Hopital de Charleroi asbl (GHdC)
6000 Charleroi
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CHU UCL Namur / Site Sainte Elisabeth
5000 Namur
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Cenantron Centro Avançado de Tratamento Oncologico Ltda
30130-090 Belo Horizonte
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Hospital Evangelico de Cachoeiro de Itapemirim
29308-014 Cachoeiro De Itapemirim
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Fundacao Universidade De Caxias Do Sul - FUCS/RS
95070-560 Caxias Do Sul
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Instituto do Câncer do Ceará - ICC
60430-230 Fortaleza
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Oncosite - Centro de Pesquisa Clinica em Oncologia LTDA
98700-000 Ijui
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Centro Des Pesquisas Clinicas da Fundacao Doutor Amaral Carvalho
17210080 Jau
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Irmandade da Santa Casa de Misericordia de Porto Alegre
90020-090 Porto Alegre
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90035-903 Porto Alegre
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90610-000 Porto Alegre
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96810-110 Santa Cruz Do Sul
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Instituto Brasiliero de Controle do Cancer IBCC
03102002 Sao Paulo
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Centre Integre de sante et de services sociaux de la Monteregie Centre
J4V 2H1 Greenfield Park
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Centre de santé et services sociaux de Rimouski-Neigette
G5L5T1 Rimouski
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Clinica Alemana de Santiago
7550000 Las Condes
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James Lind Centro de Investigacion del Cancer
4800827 Temuco
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The First Affiliated Hospital of Xinxiang Medical College
453100 Xinxiang
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Ambroise-Pare Hospital, Assistance Publique - Hopitaux de Paris
92100 Boulogne-Billancourt
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Clinique Victor Hugo, Centre de Cancerologie de la Sarthe
72000 Le Mans
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Institut de Cancer de Montpellier (ICM) - Val d'Aurelle
34928 Montpellier
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Institut de cancerologie de l'ouest (ICO)
44805 Saint-Herblain
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Hopital d'Instruction des Armees (HIA) Begin
94160 Saint-Mandé
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Centre Hospitalier de Saint-Quentin
2100 Saint-Quentin
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Institut de Cancerologie Strasbourg Europe (ICANS)
67033 Strasbourg
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CHI de Toulon la Seyne-sur-Mer Hopital Sainte Musse
83056 Toulon cedex
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Queen Elizabeth Hospital
999077 Hong Kong
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Prince of Wales Hospital
New Territories
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Soroka University Medical Center, Itzchak Rager Blvd.
84101 Beer Seva
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Shaare Zedek Medical Center
9103102 Jerusalem
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Oncology Institute, Galilee Medical Center, Route 89 Nahariya-Cabri
Nahariya
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Tel-Aviv Sourasky Medical Center
64239 Tel Aviv
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Azienda Ospedaliera San Giuseppe Moscati
Avellino
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IRCCS Fondazoine del Piemonte per l'Oncologia
10060 Candiolo
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Azienda Socio Sanitaria Territoriale di Cremona
26100 Cremona
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Ospedale Policlinico San Martino
16132 Genova
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Azienda Ospedaliero Universitaria di Modena
41124 Modena
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IRCCS Policlinico S. Matteo, Dipartimento Oncologia Ematologia-Oncologia Medica
27100 Pavia
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Azienda Sanitaria Territoriale Pesaro e Urbino (AST)
61122 Pesaro
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Ospedale Guglielmo da Saliceto AUSL di Piacenza
29100 Piacenza
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Centro di Riferimento Oncologico
33081 Pordenone
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Regina Elena Institute for Cancer Research
00144 Rome
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ASST Bergamo Ovest- ospedale di Treviglio
24047 Treviglio
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National Cancer Center Hospital East
277-0882 Chiba
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National Hospital Organization Shikoku Cancer Center
791-0280 Ehime
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National Hospital Organization Himeji Medical Center
670-8520 Hyogo
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Kanazawa University Hospital
920-8641 Ishikawa
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Niigata Cancer Center Hospital
951-8566 Niigata
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Osaka Metropolitan University Hospital
545-8586 Osaka
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Osaka Medical and Pharmaceutical University Hospital
569-8686 Osaka
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National Hospital Organization Kinki Chuo Chest Medical Center
591-8555 Osaka
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SMG - SNU Boramae Medical Center
07061 Dongjak-Gu
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Samsung Medical Center
6351 Gangnam-Gu
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National Cancer Center
410769 Goyang
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Chungbuk National University Hospital
361-711 Heungdeok-Gu
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Inha University Hospital
22332 Incheon
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Gachon University Gil Medical Center
21565 Inchon
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Kosin University Gospel Hospital
49267 Seo-gu
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Severance Hospital, Yonsei University Health System
03722 Seoul
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Asan Medical Center
05505 Seoul
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The Catholic University of Korea, Seoul St. Mary's Hospital
06591 Seoul
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Ajou University Hospital
16499 Suwon-si
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The Catholic University of Korea, Saint Vincent's Hospital
16247 Suwon
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Health Pharma Professional Research S.A. de C.V.
3100 Mexico
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Hospital Universitario Dr. Jose Eleuterio Gonzalez
64460 Mitras Centro
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Oaxaca Site Management Organization
68000 Oaxaca
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Centro de Investigacion Clinica de Oaxaca
68020 Oaxaca
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Clinical Medical Research SC.
94300 Orizaba Centro
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Clinica Integral Internacional de Oncologia S de RL de CV
72530 Puebla
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Ziekenhuis Gelderse Vallei
6716 RP Ede
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Universitair Medisch Centrum Groningen
9713 GZ Groningen
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Ziekenhuis St Jansdal
3844 DG Harderwijk
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Hospital Prof. Doutor Fernando Fonseca
2720276 Amadora
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Instituto Português de Oncologia de Lisboa Francisco Gentil
1089 Lisboa
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Centro Hospitalar Universitário Lisboa Norte - Hospital Pulido Valente
Lisboa
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Hospital Beatriz Angelo. Hospital de Loures.
2674-514 Lisbon
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Centro Hospitalar Universitario Sao Joao, EPE
4202-451 Porto
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Unidade Local de Saude de Matosinhos EPE - Hospital Pedro Hispano SA
4464-513 Senhora da Hora
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Tang Tock Seng Hospital
308433 Singapore
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Hospital Clinic de Barcelona
08036 Barcelona
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Hospital de la Santa Creu i de Sant Pau
08041 Barcelona
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Hospital Universitari Dexeus (USP Institut Universitari Dexeus/Hospital Universitari Quiron Dexeus)
8028 Barcelona
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Hospital Universitari Vall D'Hebron
8035 Barcelona
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14004 Cordoba
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35016 Las Palmas de G.C.
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28020 Madrid
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Hospital Universitario Puerta de Hierro de Majadahonda
28222 Majadahonda
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41009 Sevilla
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41014 Seville
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Instituto Valenciano De Oncologia (IVO)
46009 Valencia
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46015 Valencia
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46015 Valencia
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Changhua Christian Hospital
500-06 Changhua City
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Kaohsiung Medical University Chung-Ho Memorial Hospital
807 Kaohsiung
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Chang Gung Memorial Hospital Kaohsiung
83301 Kaohsiung
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National Cheng Kung University Hospital
70403 Tainan
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National Taiwan University Hospital
100 Taipei City
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Taipei Veterans General Hospital
10002 Taipei
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Chang Gung Memorial Hospital Linkou Branch of the Chang Gung Medical Foundation
33305 Taoyuan City
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Ankara Bilkent Sehir Hastanesi
06550 Ankara
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Dr. Abdurrahman Yurtaslan Ankara Onkoloji Egitim ve Arastirma Hastanesi
6200 Ankara
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Trakya University Faculty of Medicine
22030 Edirne
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Istanbul University Cerrahpasa Medical Faculty Hospital
34098 Fatih
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Goztepe Prof. Dr. Suleyman Yalcın Sehir Hastanesi
34093 Istanbul
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34303 Kaakaekmece
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Studien-Informationen

Brief Summary:

The primary objective of this study is to compare the effect of zimberelimab (ZIM) and

domvanalimab (DOM) in combination with chemotherapy relative to pembrolizumab (PEMBRO) in

combination with chemotherapy on progression-free survival (PFS) and overall survival (OS) in

patients with untreated metastatic non-small cell lung cancer with no actionable genomic

alteration.

Ein-/Ausschlusskriterien

Key Inclusion Criteria:

- Life expectancy ≥ 3 months.

- Pathologically documented NSCLC that meets both of the criteria below:

- Have documented evidence of Stage IV NSCLC disease at the time of enrollment

(based on American Joint Committee on Cancer (AJCC), Eighth Edition).

- Have documented negative test results for epidermal growth factor receptor (EGFR)

and anaplastic lymphoma kinase (ALK) mutations.

- Have no actionable genomic alterations such as ROS proto-oncogene 1 (ROS1),

neurotrophic tyrosine receptor kinase (NTRK), proto-oncogene B-raf (BRAF), RET

mutations, or other driver oncogenes with approved frontline therapies.

- Have not received prior systemic treatment for metastatic NSCLC.

- Measurable disease per RECIST v1.1 criteria by investigator assessment.

- Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 or 1.

- Have adequate organ functions.

Key Exclusion Criteria:

- Have mixed small-cell lung cancer (SCLC) and NSCLC histology.

- Positive serum pregnancy test or individuals who are breastfeeding or have plans to

breastfeed during the study period.

- Received prior treatment with any anti-PD-1, anti-PD-L1, or any other antibody

targeting an immune checkpoint.

- Known hypersensitivity to the study drug, its metabolites, or formulation excipient.

- Have an active second malignancy or have had an active second malignancy within 3

years prior to enrollment.

- Have an active autoimmune disease that required systemic treatment in past 2 years

(i.e., with use of disease-modifying agents, corticosteroids, or immunosuppressive

drugs).

- Are receiving chronic systemic steroids.

- Have significant third-space fluid retention.

- Have untreated central nervous system (CNS) metastases and/or carcinomatous

meningitis.

- Active chronic inflammatory bowel disease (ulcerative colitis, Crohn's disease) or

gastrointestinal perforation within 6 months of enrollment.

- Has a history of (noninfectious) pneumonitis/interstitial lung disease that required

steroids or has current pneumonitis/interstitial lung disease.

- Has had an allogenic tissue/solid organ transplant.

- Have received a live-virus vaccination within 30 days of planned treatment start.

Seasonal flu and COVID-19 vaccines that do not contain live virus are permitted.

- Have known active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Studien-Rationale

Primary outcome:

1. Progression-free Survival (PFS) as Assessed by Blinded Independent Central Review (BICR) per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 (Time Frame - Up to 31 months):
PFS is defined as the time from the date of randomization until disease progression (PD) or death from any cause, whichever comes first.

2. Overall Survival (OS) (Time Frame - Up to 58 months):
OS is defined as the time from the date of randomization to the date of death from any cause.

Secondary outcome:

1. Objective Response Rate (ORR) as Assessed by BICR per RECIST Version 1.1 (Time Frame - Up to 58 Months):
ORR is defined as the proportion of participants who have achieved a complete response (CR) or partial response (PR) that is confirmed at least 4 weeks later.

2. Duration of Response (DOR) as Assessed by BICR per RECIST Version 1.1 (Time Frame - Up to 58 Months):
DOR is defined as the time from the first response (CR or PR), to the first documented PD or death from any cause, whichever comes first.

3. Percentage of Participants Experiencing Treatment-emergent Adverse Events (TEAEs) (Time Frame - First dose date up to 58 months plus 30 days)

4. Percentage of Participants Experiencing Clinical Laboratory Abnormalities (Time Frame - First dose date up to 58 months plus 30 days)

5. Time to First Symptom Deterioration in Non-small Cell Lung Cancer Symptom Assessment Questionnaire (NSCLC-SAQ) Total Score (Time Frame - Baseline, Up to 58 Months):
The NSCLC-SAQ is a patient reported outcome measure with seven items assessing five symptom concepts of NSCLC: cough, pain, dyspnea, fatigue, and appetite. Each item is rated using a five-point verbal rating scale from "No <symptom> At All" to "Very severe <symptom>" or from "Never to Always," corresponding to a score of 0 to 4. The sum of all 5 domain scores will be computed, if any scores are missing, a total score will not be computed. The total score ranges between 0 and 20 with higher scores indicating more severe symptoms.

Studien-Arme

  • Experimental: Zimberelimab (ZIM) +Domvanalimab (DOM) + Chemotherapy
    Participants will receive ZIM 360 mg + DOM 1200 mg (up to 35 doses) with chemotherapy every 3 weeks (Q3W) on Day 1 of each 21-day cycle. Choice of chemotherapy is dependent on histology. Participants with nonsquamous histology will receive cisplatin 75 mg/m^2 or carboplatin area under the concentration versus time curve (AUC)5 + pemetrexed 500 mg/m^2 Q3W for first 4 cycles. After the completion of the first 4 cycles, participants with nonsquamous histology may continue with maintenance pemetrexed 500 mg/m^2 Q3W until disease progression or intolerable toxicities. Participants with squamous histology will receive carboplatin AUC 6 Q3W with paclitaxel 200 mg/m^2 Q3W or nab-paclitaxel 100 mg/m^2 weekly (QW) for first 4 cycles.
  • Active Comparator: Pembrolizumab (PEMBRO) + Chemotherapy
    Participants will receive PEMBRO 200 mg (up to 35 doses) with chemotherapy Q3W on Day 1 of each 21-day cycle. Choice of chemotherapy is dependent on histology. Participants with nonsquamous histology will receive cisplatin 75 mg/m^2 or carboplatin AUC 5 + pemetrexed 500 mg/m^2 Q3W for first 4 cycles. After the completion of the first 4 cycles, participants with nonsquamous histology may continue with maintenance pemetrexed 500 mg/m^2 Q3W until disease progression or intolerable toxicities. Participants with squamous histology will receive carboplatin AUC 6 Q3W with paclitaxel 200 mg/m^2 Q3W or nab-paclitaxel 100 mg/m^2 weekly (QW) for first 4 cycles.
  • Experimental: Zimberelimab (ZIM) + Chemotherapy
    Participants will receive ZIM 360 mg (up to 35 doses) with chemotherapy Q3W on Day 1 of each 21-day cycle. Choice of chemotherapy is dependent on histology. Participants with nonsquamous histology will receive cisplatin 75 mg/m^2 or carboplatin AUC 5 + pemetrexed 500 mg/m^2 Q3W for first 4 cycles After the completion of the first 4 cycles, participants with nonsquamous histology may continue with maintenance pemetrexed 500 mg/m^2 Q3W until disease progression or intolerable toxicities. Participants with squamous histology will receive carboplatin AUC 6 Q3W with paclitaxel 200 mg/m^2 Q3W or nab-paclitaxel 100 mg/m^2 weekly (QW) for first 4 cycles.

Geprüfte Regime

  • Zimberelimab (GS-0122 / AB122 / ):
    Administered intravenously
  • Domvanalimab (GS-0154 / AB154 / ):
    Administered intravenously
  • Pembrolizumab (KEYTRUDA®):
    Administered intravenously
  • Carboplatin:
    Administered intravenously
  • Cisplatin:
    Administered intravenously
  • Paclitaxel:
    Administered intravenously
  • Nab-paclitaxel:
    Administered intravenously
  • Pemetrexed:
    Administered intravenously

Quelle: ClinicalTrials.gov


Sie können folgenden Inhalt einem Kollegen empfehlen:

"Zimberelimab and Domvanalimab in Combination With Chemotherapy Versus Pembrolizumab With Chemotherapy in Patients With Untreated Metastatic Non-Small Cell Lung Cancer"

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