- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07544654
En studie hos personer med avansert ekstrapulmonal nevroendokrin kreft for å sammenligne behandling med obrixtamig pluss karboplatin og etoposid med standard kjemoterapi
En fase III, multisenter, åpen, randomisert, kontrollert studie av intravenøs Obrixtamig i kombinasjon med karboplatin og etoposid vs. karboplatin og etoposid som førstelinjebehandling hos DLL3-positive pasienter med ikke-opererbart lokalt avansert eller metastatisk ekstrapulmonalt nevroendokrine karsinom
This study is open to adults with advanced extrapulmonary neuroendocrine cancer. The purpose of this study is to find out if a study medicine called obrixtamig plus standard chemotherapy (carboplatin and etoposide) improves survival when compared to standard chemotherapy (carboplatin and etoposide) alone. Obrixtamig is an antibody-like molecule that may help the immune system fight cancer. Another purpose of the study is to test a medical device being developed to measure levels of the tumour marker delta-like ligand 3 (DLL3).
Participants are put into 2 groups randomly, which means by chance. One group (treatment arm) receives obrixtamig and standard chemotherapy followed by obrixtamig alone for up to 3 years. The other group (control arm) receives standard chemotherapy without obrixtamig for about 4 months. All treatments are given as infusions into a vein.
During the study, participants in both groups visit the study site regularly. Participants in the treatment arm stay overnight at the study site following the first 2 obrixtamig treatments. The doctors regularly check participants' health and take note of any unwanted effects. At some of the visits, doctors check the size of the tumour(s). The results are compared between the 2 groups to see whether the treatment works.
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Fase
- Fase 3
Kontakter og plasseringer
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Arizona
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Florida
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Illinois
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Maryland
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Massachusetts
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Minnesota
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Missouri
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Tennessee
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Washington
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Clichy, Frankrike, 92110
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Beersheba, Israel, 84101
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Florence, Italia, 50134
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Aichi, Nagoya, Japan, 464-8681
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Chiba, Kashiwa, Japan, 277-8577
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Ehime, Matsuyama, Japan, 791-0280
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Fukuoka, Fukuoka, Japan, 812-8582
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Hokkaido, Sapporo, Japan, 060-8648
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Ishikawa, Kanazawa, Japan, 920-8641
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Kanagawa, Yokohama, Japan, 241-8515
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Kyoto, Kyoto, Japan, 606-8507
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Miyagi, Sendai, Japan, 980-8574
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Okayama, Okayama, Japan, 700-8558
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Osaka, Osaka, Japan, 541-8567
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Shizuoka, Sunto-gun, Japan, 411-8777
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Tokyo, Chuo-ku, Japan, 104-0045
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Beijing, Kina, 100142
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Beijing, Kina, 102200
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Changchun, Kina, 130021
- Har ikke rekruttert ennå
- The First Hospital of Jilin University
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- E-post: china@bitrialsupport.com
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Changsha, Kina, 410008
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- Xiangya Hospital, Central South University
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- E-post: china@bitrialsupport.com
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Changsha, Kina, 410013
- Har ikke rekruttert ennå
- Hunan Province Tumor Hospital
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- E-post: china@bitrialsupport.com
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Chengdu, Kina, 610041
- Rekruttering
- West China Hospital, Sichuan University
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Chengdu, Kina, 610041
- Rekruttering
- Sichuan Cancer Hospital
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Chongqing, Kina, 400000
- Rekruttering
- Chongqing University Affiliated Cancer Hospital
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Fuzhou, Kina, 350014
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- Fujian Cancer Hospital
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Guangzhou, Kina, 510080
- Rekruttering
- The First Affiliated Hospital,Sun Yat-sen University
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Hangzhou, Kina, 310016
- Rekruttering
- Sir Run Run Shaw Hospital, Zhejiang University, School of Medicine
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- E-post: china@bitrialsupport.com
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Harbin, Kina, 150081
- Rekruttering
- Harbin Medical University Cancer Hospital
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Jinan, Kina, 250117
- Rekruttering
- Shandong Cancer Hospital
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Jinan, Kina, 250012
- Rekruttering
- Qilu Hospital, Shangdong University
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Linyi, Kina, 276034
- Rekruttering
- Linyi Cancer Hospital
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Luoyang, Kina, 471003
- Rekruttering
- The First Affiliated Hospital of Henan University of Science and Technology
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Nanning, Kina, 530021
- Rekruttering
- The Affiliated Cancer Hospital, Guangxi Medical University
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Shanghai, Kina, 200080
- Rekruttering
- Shanghai General Hospital
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- E-post: china@bitrialsupport.com
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Wuhan, Kina, 430000
- Rekruttering
- Hubei Cancer Hospital
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- E-post: china@bitrialsupport.com
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Xi'an, Kina, 710061
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- First Affiliated Hospital of Xi'an JiaoTong University
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- E-post: china@bitrialsupport.com
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Xiamen, Kina, 361003
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- First Affiliated Hospital of Xiamen University
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- E-post: china@bitrialsupport.com
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Zhengzhou, Kina, 450052
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- The First Affiliated Hospital of Zhengzhou University
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- E-post: china@bitrialsupport.com
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Guadalajara, Jalisco, Mexico, 44329
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- Centro Medico Nacional de Occidente/ Centro De Investigacion Biomedica De Occidente
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Ta kontakt med:
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- Telefonnummer: 018000623749
- E-post: mexico@bitrialsupport.com
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Mexico City, Mexico, 03100
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- Health Pharma Professional Research S.A. de C.V.
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Ta kontakt med:
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- Telefonnummer: 018000623749
- E-post: mexico@bitrialsupport.com
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México, Mexico, 06760
- Har ikke rekruttert ennå
- Centro Oncologico Personalizado
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Ta kontakt med:
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- Telefonnummer: 018000623749
- E-post: mexico@bitrialsupport.com
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Toluca, Mexico, 50180
- Rekruttering
- Centro Oncologico Estatal ISSEMYM
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Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 018000623749
- E-post: mexico@bitrialsupport.com
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Zapopan, Mexico, 45060
- Har ikke rekruttert ennå
- Instituto Jaliciense de Cancerología
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Ta kontakt med:
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- Telefonnummer: 018000623749
- E-post: mexico@bitrialsupport.com
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Amsterdam, Nederland, 1066CX
- Har ikke rekruttert ennå
- Nederlands Kanker Instituut - Antoni van Leeuwenhoek Amsterdam (METC AVL)
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- Telefonnummer: 08000204613
- E-post: nederland@bitrialsupport.com
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Groningen, Nederland, 9713 GZ
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- Universitair Medisch Centrum Groningen
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Ta kontakt med:
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- Telefonnummer: 08000204613
- E-post: nederland@bitrialsupport.com
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Maastricht, Nederland, 6229 HX
- Har ikke rekruttert ennå
- Maastricht University Medisch Centrum
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- Telefonnummer: 08000204613
- E-post: nederland@bitrialsupport.com
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Rotterdam, Nederland, 3015 GD
- Rekruttering
- Erasmus Medisch Centrum
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Ta kontakt med:
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Grafton / Auckland, New Zealand, 1023
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- Auckland City Hospital
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Ta kontakt med:
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- Telefonnummer: 0800440725
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Bergen, Norge, 5021
- Rekruttering
- Haukeland Universitetssykehus
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Ta kontakt med:
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- Telefonnummer: 80058261
- E-post: norge@bitrialsupport.com
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Oslo, Norge, N-0379
- Rekruttering
- Oslo Universitetssykehus HF, Radiumhospitalet
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Ta kontakt med:
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- Telefonnummer: 80058261
- E-post: norge@bitrialsupport.com
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Stavanger, Norge, 4011
- Rekruttering
- Helse Stavanger, Stavanger Universitetssykehus
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Ta kontakt med:
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- Telefonnummer: 80058261
- E-post: norge@bitrialsupport.com
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Trondheim, Norge, 7030
- Har ikke rekruttert ennå
- St. Olavs Hospital, Universitetssykehuset i Trondheim
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Ta kontakt med:
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- Telefonnummer: 80058261
- E-post: norge@bitrialsupport.com
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Gdansk, Polen, 80-214
- Har ikke rekruttert ennå
- Medical University Gdansk
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Ta kontakt med:
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- Telefonnummer: 008001218830
- E-post: polska@bitrialsupport.com
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Katowice, Polen, 40514
- Har ikke rekruttert ennå
- Silesian Medical University in Katowice
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Ta kontakt med:
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- Telefonnummer: 008001218830
- E-post: polska@bitrialsupport.com
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Lisbon, Portugal, 1500-458
- Rekruttering
- Hospital Lusiadas Lisboa
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Ta kontakt med:
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- Telefonnummer: 800856070
- E-post: portugal@bitrialsupport.com
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Lisbon, Portugal, 1099-023
- Har ikke rekruttert ennå
- IPO Lisboa Francisco Gentil, EPE
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Ta kontakt med:
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- Telefonnummer: 800856070
- E-post: portugal@bitrialsupport.com
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Lisbon, Portugal, 1699-035
- Har ikke rekruttert ennå
- Unidade Local de Saúde Santa Maria
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Ta kontakt med:
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- Telefonnummer: 800856070
- E-post: portugal@bitrialsupport.com
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Porto, Portugal, 4100-180
- Har ikke rekruttert ennå
- Hospital CUF Porto
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Ta kontakt med:
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- Telefonnummer: 800856070
- E-post: portugal@bitrialsupport.com
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Porto, Portugal, 4200-072
- Rekruttering
- IPO Porto Francisco Gentil, EPE
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Ta kontakt med:
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- Telefonnummer: 800856070
- E-post: portugal@bitrialsupport.com
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Badalona, Spania, 8916
- Har ikke rekruttert ennå
- Institut Català d'Oncologia de Badalona
-
Ta kontakt med:
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- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
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Barcelona, Spania, 08035
- Rekruttering
- Hospital Universitari Vall d'Hebron
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Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
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L'Hospitalet Del Llobregat, Spania, 08908
- Har ikke rekruttert ennå
- Hospital Duran i Reynals
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Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
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Madrid, Spania, 28041
- Rekruttering
- Hospital Universitario 12 de Octubre
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
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Madrid, Spania, 28040
- Rekruttering
- Hospital Universitario Fundacion Jimenez Diaz
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
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Madrid, Spania, 28034
- Rekruttering
- Hospital Universitario Ramon Y Cajal
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
-
Málaga, Spania, 29010
- Rekruttering
- Hospital Regional Universitario de Malaga
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
-
Pamplona, Spania, 31008
- Rekruttering
- Hospital Universitario de Navarra
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
-
Santander, Spania, 39008
- Rekruttering
- Hospital Universitario Marqués de Valdecilla
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
-
Seville, Spania, 41013
- Rekruttering
- Hospital Virgen del Rocio
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
-
Valencia, Spania, 46010
- Har ikke rekruttert ennå
- Hospital Clinico De Valencia (INCLIVA)
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 900876092
- E-post: espana@bitrialsupport.com
-
-
-
-
-
Cambridge, Storbritannia, CB2 0QQ
- Har ikke rekruttert ennå
- Addenbrooke's Hospital
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08000514022
- E-post: unitedkingdom@bitrialsupport.com
-
Edinburgh, Storbritannia, EH4 2XU
- Rekruttering
- Western General Hospital
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08000514022
- E-post: unitedkingdom@bitrialsupport.com
-
Manchester, Storbritannia, M20 4BX
- Rekruttering
- The Christie
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08000514022
- E-post: unitedkingdom@bitrialsupport.com
-
-
-
-
-
Gothenburg, Sverige, 41345
- Har ikke rekruttert ennå
- Sahlgrenska Universitetsjukhuset
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0200880001
- E-post: sverige@bitrialsupport.com
-
Lund, Sverige, 22185
- Rekruttering
- Skånes universitetssjukhus
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0200880001
- E-post: sverige@bitrialsupport.com
-
Uppsala, Sverige, 751 85
- Rekruttering
- Uppsala University Hospital
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0200880001
- E-post: sverige@bitrialsupport.com
-
-
-
-
-
Seoul, Sør -Korea, 05505
- Rekruttering
- Asan Medical Center
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0808802084
- E-post: namhan@bitrialsupport.com
-
Seoul, Sør -Korea, 03080
- Rekruttering
- Seoul National University Hospital
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0808802084
- E-post: namhan@bitrialsupport.com
-
Seoul, Sør -Korea, 06351
- Rekruttering
- Samsung Medical Center
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0808802084
- E-post: namhan@bitrialsupport.com
-
Seoul, Sør -Korea, 03722
- Rekruttering
- Severance Hospital
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0808802084
- E-post: namhan@bitrialsupport.com
-
-
-
-
-
Tainan, Taiwan, 70403
- Rekruttering
- National Cheng Kung University Hospital
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0809092098
- E-post: taiwan@bitrialsupport.com
-
Taipei, Taiwan, 112201
- Rekruttering
- Taipei Veterans General Hospital
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0809092098
- E-post: taiwan@bitrialsupport.com
-
Taoyuan City, Taiwan, 333
- Rekruttering
- Chang Gung Memorial Hospital, Linkou
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0809092098
- E-post: taiwan@bitrialsupport.com
-
-
-
-
-
Brno, Tsjekkia, 65653
- Rekruttering
- Masaryk Memorial Cancer Institute
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 00441144040048
- E-post: support@bitrialsupport.com
-
Hradec Králové, Tsjekkia, 50005
- Har ikke rekruttert ennå
- University Hospital Hradec Kralove (FNHK)
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 00441144040048
- E-post: support@bitrialsupport.com
-
-
-
-
-
Berlin, Tyskland, 12559
- Rekruttering
- DRK Kliniken Berlin Köpenick
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
-
Bonn, Tyskland, 53127
- Har ikke rekruttert ennå
- Universitätsklinikum Bonn AöR
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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Cologne, Tyskland, 50937
- Har ikke rekruttert ennå
- Universitätsklinikum Köln (AöR)
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
-
Dresden, Tyskland, 01307
- Har ikke rekruttert ennå
- Technische Universität Dresden
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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Düsseldorf, Tyskland, 40225
- Har ikke rekruttert ennå
- Universitätsklinikum Düsseldorf
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Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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Erlangen, Tyskland, 91054
- Har ikke rekruttert ennå
- Universitätsklinikum Erlangen
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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Freiburg im Breisgau, Tyskland, 79106
- Har ikke rekruttert ennå
- Universitätsklinikum Freiburg
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Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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Hamburg, Tyskland, 20099
- Rekruttering
- Asklepios Klinik St Georg
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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Heidelberg, Tyskland, 69120
- Rekruttering
- Universitätsklinikum Heidelberg
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Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
-
Mainz, Tyskland, 55131
- Har ikke rekruttert ennå
- Universitätsmedizin der Johannes Gutenberg-Universität Mainz
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
-
Münster, Tyskland, 48149
- Har ikke rekruttert ennå
- Westfälische Wilhelms-Universität Münster
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
-
Tübingen, Tyskland, 72076
- Rekruttering
- Universitätsklinikum Tübingen
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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Würzburg, Tyskland, 97078
- Har ikke rekruttert ennå
- Universitätsklinikum Würzburg AÖR
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 08007234742
- E-post: deutschland@bitrialsupport.com
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-
-
-
-
Graz, Østerrike, 8036
- Har ikke rekruttert ennå
- Medical University of Graz
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0800017900
- E-post: oesterreich@bitrialsupport.com
-
Vienna, Østerrike, 1090
- Har ikke rekruttert ennå
- Medical University of Vienna
-
Ta kontakt med:
- Boehringer Ingelheim
- Telefonnummer: 0800017900
- E-post: oesterreich@bitrialsupport.com
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Patients with poorly differentiated unresectable locally advanced or metastatic extrapulmonary neuroendocrine carcinoma (epNEC) with Ki-67 >20% or mitotic rate mitotic rate with number of mitoses >20 per 2 mm2, regardless of primary site (including site of unknown origin)
- Patients with tumours with mixed histologies are eligible only if neuroendocrine carcinoma component is predominant and represents more than 70% of the overall tumour tissue
- No prior systemic treatment for unresectable locally advanced or metastatic epNEC (except for the completed one cycle of standard platinum + etoposide). Prior peri-operative chemotherapy or -radiation for curative intention is allowed if at least 6 months have elapsed between completion of this therapy and diagnosis of unresectable locally advanced or metastatic disease
- Patients who have finished one cycle of standard platinum + etoposide regimen as first-line treatment (Cycle 0: etoposide with carboplatin or cisplatin, administered at a minimum dose of cisplatin 75 mg/m2 or carboplatin area under the curve (AUC) 5 and etoposide 80 mg/m2) prior to randomisation
- Patients must comply with criteria for receiving further chemotherapy treatment as first-line standard of care (SoC) treatment within 28 days after the start of the initial chemotherapy (Cycle 0)
- Adequate archival Formalin-Fixed Paraffin-Embedded (FFPE) tumour tissue, as specified in the Laboratory Manual, must be available for central laboratory analysis of Delta-like ligand 3 (DLL3) expression status. Tumours must be positive (as defined in the diagnostic study protocol) for DLL3 expression status assessed by investigational VENTANA DLL3 (SP347) RxDx Assay
- Eastern Cooperative Oncology Group (ECOG) score of 0 or 1
- Male or female participants ≥18 years old and at least at the legal age of consent in countries where it is greater than 18 years at the time of signature of the informed consent form (ICF) Further inclusion criteria apply.
Exclusion Criteria:
- Presence of leptomeningeal disease and/or carcinomatous meningitis
- Patients with diagnosis of Merkel cell carcinoma or medullary thyroid carcinoma
- Patients with neuroendocrine prostate cancer
- Patients with well-differentiated neuroendocrine tumours of any grade according to the world health organization (WHO) classification, 5th edition
- Patients with a history of well differentiated Neuroendocrine tumour (NET) tumour that transformed into poorly differentiated Neuroendocrine carcinoma (NEC)
- Previous treatment with obrixtamig or other DLL3-targeting therapies (e.g. T-cell engager (TcEs), cell therapies, antibody-drug conjugates, or radiopharmaceuticals)
- Previous treatment with anti-PD-1 or programmed death ligand 1 (PD-L1) therapies during the one cycle of standard platinum + etoposide first-line chemotherapy (Cycle 0)
- Toxicity from previous treatments that has not resolved to ≤ Common Terminology Criteria for Adverse Events (CTCAE) Grade 1 or grade prior to Cycle 0. Participants with alopecia any grade, CTCAE ≤Grade 2 asthenia/fatigue, amenorrhea/menstrual disorders any grade, CTCAE ≤Grade 2 peripheral neuropathy, and/or CTCAE ≤Grade 2 endocrinopathies controlled by replacement therapy, and toxicities, which are considered irreversible but stable for at least 4 weeks, per Investigator judgement may be eligible Further exclusion criteria apply.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Obrixtamig + carboplatin + etoposide
Treatment arm |
Obrixtamig Carboplatin Etoposide Ventana DLL3 RxDx assay |
|
Aktiv komparator: Carboplatin + etoposide
Control arm |
Carboplatin Etoposide Ventana DLL3 RxDx assay |
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Overall survival (OS)
Tidsramme: Up to 38 months
|
defined as the time from randomisation until death from any cause |
Up to 38 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Forekomst av behandlingsutløst grad 3 eller høyere Cytokinfrigjøringssyndrom (CRS)
Tidsramme: Inntil 38 måneder
|
Inntil 38 måneder
|
|
|
Forekomst av behandlingsrelatert Grad 3 eller høyere immun-celle-assosiert nevrotoksisitetssyndrom (ICANS)
Tidsramme: Opptil 38 måneder
|
Opptil 38 måneder
|
|
|
Forekomst av behandlingsutløste uønskede hendelser (AEs) som fører til permanent avbrudd av prøvemedisinering i behandlingsperioden
Tidsramme: Opptil 38 måneder
|
Opptil 38 måneder
|
|
|
Forekomst av behandlingsrelaterte uønskede hendelser som fører til dosemodifisering av prøvemedikamentet (dvs. doseavbrudd, doseforsinkelse, dosereduksjon)
Tidsramme: Opptil 38 måneder
|
Opptil 38 måneder
|
|
|
Progression-free survival (PFS)
Tidsramme: Up to 38 months
|
defined as the time from randomisation until the earliest date of disease progression according to RECIST 1.1 based on investigator assessments or death from any cause, whichever occurs first |
Up to 38 months
|
|
Change from baseline to Week 19 in the physical functioning domain of the EORTC QLQ-C30
Tidsramme: At baseline, up to week 19
|
European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire C30 (EORTC QLQ C30) includes 1 global health status/QoL scale, 5 functional scales, 3 symptoms scales and 6 single items to assess dyspnea, insomnia, appetite loss, constipation, diarrhoea and financial difficulties. Each score 0-100. Global health status higher = better, functional scale higher = better, symptom scale higher = worse |
At baseline, up to week 19
|
|
Objective response (OR)
Tidsramme: Up to 38 months
|
defined as a best overall response of complete response (CR) or partial response (PR) according to RECIST 1.1 (based on investigator assessments) from randomisation until the earliest date of disease progression, death, last evaluable tumour assessment before the start of next line of anti-cancer treatment, loss to follow-up, or withdrawal of consent |
Up to 38 months
|
|
Duration of response (DoR)
Tidsramme: Up to 38 months
|
defined as the time from the first documented OR according to RECIST 1.1 until the earliest date of disease progression or death among patients with objective response based on investigator assessments |
Up to 38 months
|
|
Disease control (DC)
Tidsramme: Up to 38 months
|
defined as best overall response of complete response (CR) or partial response (PR) or stable disease (SD) where best overall response is defined according to RECIST 1.1 based on investigator assessments from randomisation until the earliest of disease progression, death or last evaluable tumour assessment before start of next line of anti-cancer treatment, loss to follow-up or withdrawal of consent |
Up to 38 months
|
Samarbeidspartnere og etterforskere
Sponsor
Publikasjoner og nyttige lenker
Hjelpsomme linker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 1438-0011
- U1111-1328-6623 (Registeridentifikator: WHO International Clinical Trials Registry Platform (ICTRP))
- 2025-523869-22-00 (Registeridentifikator: CTIS)
- 2025 (U.S. NIH-stipend/kontrakt)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
Once the criteria in section "Time Frame" are fulfilled, researchers can use the following link https://www.clinicalstudies.boehringer-ingelheim.com/msw/datasharing to request access to the clinical study documents regarding this study, and upon a signed "Document Sharing Agreement".
Furthermore, researchers can request access to the clinical study data, for this and other listed studies, after the submission of a research proposal and according to the terms outlined in the website.
IPD-delingstidsramme
One year after the approval has been granted by major Regulatory Authorities and after the primary manuscript has been accepted for publication, or after termination of the development program.
Tilgangskriterier for IPD-deling
For study documents - upon signing of a 'Document Sharing Agreement'.
For study data - 1. after the submission and approval of the research proposal (checks will be performed by the sponsor and/or the independent review panel, including checking that the planned analysis does not compete with sponsor's publication plan); 2. and upon signing of a legal agreement.
IPD-deling Støtteinformasjonstype
- STUDY_PROTOCOL
- SEVJE
- CSR
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .