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The phase I/II eNRGy trial: Zenocutuzumab in patients with cancers harboring NRG1 gene fusions

Authors
 Kim, Dong-Wan  ;  Schram, Alison M.  ;  Hollebecque, Antoine  ;  Nishino, Kazumi  ;  Macarulla, Teresa  ;  Rha, Sun Young  ;  Duruisseaux, Michael  ;  Liu, Stephen, V  ;  Al Hallak, Mohammed Najeeb  ;  Umemoto, Kumiko  ;  Wesseler, Claas  ;  Cleary, James M.  ;  Springfeld, Christoph  ;  Neuzillet, Cindy  ;  Joe, Andrew  ;  Jauhari, Shekeab  ;  Ford, Jim  ;  Goto, Koichi 
Citation
 FUTURE ONCOLOGY, Vol.20(16) : 1057-1067, 2024-02 
Journal Title
FUTURE ONCOLOGY
ISSN
 1479-6694 
Issue Date
2024-02
Keywords
eNRGy trial ; HER2 ; HER3 ; NRG1+ ; NRG1 fusion ; NSCLC ; PDAC ; recruiting ; Zeno ; Zenocutuzumab
Abstract
NRG1 gene fusions are rare mutations that cause cancer cells to grow. These fusions are found in many different types of cancer. Tumors with NRG1 gene fusions do not respond well to standard treatment options. Zenocutuzumab, or Zeno, is a treatment that is being tested to see if it can stop cancer that is growing because of NRG1 gene fusions. Here, we describe the reasoning for and design of an ongoing clinical trial (eNRGy) designed to study the efficacy (how well it works) and safety of Zeno in patients with cancer that has NRG1 gene fusions. The eNRGy trial is recruiting patients with cancer that has NRG1 gene fusions, including non-small-cell lung cancer, pancreatic cancer and others. Patients who join this trial will receive Zeno once every 2 weeks until their cancer grows. The main goal (primary end point) of this trial is to determine the percentage of patients whose tumors decrease in size by 30% or more. The eNRGy trial is currently enrolling patients. For more information, refer to ClinicalTrials.gov (Identifier: NCT02912949), visit https://nrg1.com/, or call 1-833-NRG-1234.
DOI
10.2217/fon-2023-0824
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Rha, Sun Young(라선영) ORCID logo https://orcid.org/0000-0002-2512-4531
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200229
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