| Literature DB >> 31755321 |
John Nemunaitis1,2, Sebastian Bauer3, Jean-Yves Blay4, Khalil Choucair1, Hans Gelderblom5, Suzanne George6, Patrick Schöffski7, Margaret von Mehren8, John Zalcberg9, Haroun Achour10, Rodrigo Ruiz-Soto10, Michael C Heinrich11.
Abstract
Ripretinib (DCC-2618) is a novel, type II tyrosine switch control inhibitor designed to broadly inhibit activating and drug-resistant mutations in KIT and PDGFRA. Ripretinib has emerged as a promising investigational agent for the treatment of gastrointestinal stromal tumor owing to targeted inhibition of secondary resistance mutations that may develop following treatment with prior line(s) of tyrosine kinase inhibitors. Here we describe the rationale and design of intrigue (NCT03673501), a global, randomized (1:1), open-label, Phase III study comparing the safety and efficacy of ripretinib versus sunitinib in patients with advanced gastrointestinal stromal tumor following imatinib. The primary end point is progression-free survival and key secondary objectives include objective response rate and overall survival. Clinical Trial Registration: NCT03673501.Entities:
Keywords: DCC-2618; KIT; PDGFRA; Phase III trial; gastrointestinal stromal tumor; receptor tyrosine kinase; ripretinib; sarcoma; targeted therapy; tyrosine kinase inhibitor
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Year: 2019 PMID: 31755321 DOI: 10.2217/fon-2019-0633
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404