FDA Approves Encorafenib with Binimetinib for Metastatic Non-Small Cell Lung Cancer with a BRAF V600E Mutation
It also approved the FoundationOne CDx (tissue) and FoundationOne Liquid CDx (plasma) as companion diagnostics
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It also approved the FoundationOne CDx (tissue) and FoundationOne Liquid CDx (plasma) as companion diagnostics
Evidence for efficacy is based on the results from the BCHILD study
It is intended for patients who require systemic treatment following platinum-based chemotherapy with or without immunotherapy
Findings from the phase II study
Findings from the cohort E of CHRYSALIS study
Findings from the BTC cohort of SGNTUC-019 study
It is intended as monotherapy for the adjuvant treatment of adults with non-small cell lung cancer who are at high risk of recurrence following complete resection and platinum-based chemotherapy
Findings from the ALYCANTE study
Findings from the MAGENTA study
Project Renewal is limited to updating labelling information for older oncology drugs to ensure information is clinically meaningful and scientifically up-to-date
It is intended for the treatment of adult patients with newly diagnosed FLT3-ITD positive AML
Findings from the HERTHENA-Lung01 study
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