WebOct 5, 2024 · In the CHRYSALIS trial, patients received 1050 mg or 1400 mg of single-agent amivantamab or 1050 mg or 1400 mg of amivantamab plus 240 mg of lazertinib or … WebAug 19, 2024 · CHRYSALIS ( NCT02609776) is a Phase 1 open-label, multicenter, first-in-human study to evaluate the safety, pharmacokinetics and preliminary efficacy of …
MARIPOSA: phase 3 study of first-line amivantamab
WebDec 3, 2024 · The application was based on findings from the single-agent arm of the phase 1 CHRYSALIS trial (NCT02609776). ... Part 1 of the trial was a dose-escalation design, where patients were given 140 mg ... WebNov 20, 2015 · Amivantamab in EGFR Exon 20 Insertion-Mutated Non-Small-Cell Lung Cancer Progressing on Platinum Chemotherapy: Initial Results From the CHRYSALIS … greenpath maldives
Amivantamab Shows Promise in NSCLC With Hard-to-Treat EGFR …
WebSep 7, 2024 · Patients are eligible post- chemo and post-MET TKI (s). Contact: [email protected]. Trial Eligibility Criteria and Locations. Trial ID: NCT02609776. Condition: Non-Small Cell Lung Cancer Intervention: Parallel Assignment Study Type: Interventional. Study Phase: I. Study Sponsor: Janssen Research & Development, LLC … 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. WebFeb 18, 2024 · Its safety and antileukaemic activity as a single agent in an FLT3 mutation-enriched R/R AML population was initially documented in the phase 1/2 CHRYSALIS trial [1]. The subsequent phase 3 ADMIRAL trial demonstrated that gilteritinib treatment was associated with a longer median overall survival (OS) in FLT3 -mutated patients … fly prague to zurich