WebAug 5, 2024 · The phase I CHRYSALIS trial found that patients with non-small cell lung cancer who carry a MET exon 14 skipping mutation responded well to treatment with amivantamab. The overall response rate (ORR) to the bispecific antibody was 33%, and median progression-free survival was 6.7 months. WebOct 20, 2024 · Amivantamab in EGFR Exon 20 Insertion-Mutated Non-Small-Cell Lung Cancer Progressing on Platinum Chemotherapy: Initial Results From the CHRYSALIS …
Congress Scientific Watch OncologyPRO - ESMO
WebAug 2, 2024 · CHRYSALIS, a first-in-human, phase I dose-escalation, and dose-expansion study ( NCT02609776 ), evaluates the efficacy, safety, and pharmacokinetics of amivantamab in patients with advanced NSCLC. WebSep 21, 2024 · The CHRYSALIS study (NCT02609776) is evaluating amivantamab, a fully human bispecific antibody that targets epidermal growth factor receptor (EGFR) and mesenchymal epithelial transition factor (MET) mutations, zin combination with the third-generation EGFR tyrosine kinase inhibitor (TKI) lazertinib in patients with non-small cell … highline school district registration
Final Results of the Chrysalis Trial: A First-in-Human Phase 1/2 …
WebDec 2, 2016 · Final Results of the Chrysalis Trial: A First-in-Human Phase 1/2 Dose-Escalation, Dose-Expansion Study of Gilteritinib (ASP2215) in Patients with Relapsed/Refractory Acute Myeloid Leukemia (R/R AML) ... The objectives of this phase 1/2 study were to assess gilteritinib safety/tolerability, pharmacokinetic (PK) and … WebTreatment with RYBREVANT ® was evaluated in the CHRYSALIS trial CHRYSALIS is a multicenter, open-label, multicohort study that included 129 adult patients with locally … WebJun 2, 2024 · DOI: 10.1200/JCO.2024.40.16_suppl.9006 Journal of Clinical Oncology - published online before print June 2, 2024 Amivantamab and lazertinib in patients with … highline school district news