High Response Rates Observed Following KTE-X19 CAR T-Cell Therapy in Adults with Relapsed/Refractory B-Cell Acute Lymphoblastic Leukaemia
Pivotal results of the phase II, ZUMA-3 study
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Pivotal results of the phase II, ZUMA-3 study
Data support metronomic capecitabine as a potential adjuvant therapy for nasopharyngeal carcinoma
A novel checkpoint inhibitors combination of nivolumab plus relatlimab validate dual LAG-3 and PD-1 inhibition
New indications concern the treatment of patients with multiple myeloma and light chain amyloidosis
New indication concerns the treatment of paediatric patients with high-risk first relapsed Philadelphia chromosome negative CD19-positive B-precursor ALL
Findings from the eNRGy1 global multicentre registry
The results of the CheckMate 274 study point to first immune checkpoint inhibitor prolonging the disease-free survival in this setting
FDA also approved the QIAGEN therascreen® KRAS RGQ PCR kit (tissue) and the Guardant360® CDx (plasma) as companion diagnostics
FDA also approved FoundationOne® CDx for selection of patients with FGFR2 fusion or other rearrangement as a companion diagnostic device
Findings from a follow-up analysis of data from 2 to 12 years after vaccination
New indication concerns the first-line treatment of advanced oesophageal carcinoma or gastroesophageal junction adenocarcinoma
FDA also approved the Guardant360® CDx as a companion diagnostic
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