Zenocutuzumab received accelerated approval from the FDA for the agent to treat non-small cell lung cancer (NSCLC) or ...
The FDA has granted fast track designation to LBS-007 for the treatment of patients with acute myeloid leukemia.
According to the American Lung Association, biomarker testing gaps and low screening rates continue to hinder lung cancer ...
Following a phase 1b trial, the potent and selective dual inhibitor of IRAK1 and IRAK4 received fast track designation for the treatment of patients with lower-risk myelodysplastic syndrome.
The FDA approved a companion diagnostic to identify patients with biliary tract cancer eligible for treatment with ...
Oncology nurses “play a pivotal role in guiding patients” through the genetic testing process, an expert explained.
The FDA received a biologics license application for accelerated approval of RP1 plus nivolumab for advanced, pretreated ...
The FDA granted an accelerated approval to zanidatamab-hrii for previously treated, unresectable or metastatic HER2-positve ...
Anito-Cel Shows 95% OS Rate in Relapsed/Refractory Myeloma ...
The FDA accepted a supplemental new drug application to darolutamide plus androgen deprivation therapy for metastatic hormone ...
Clinicians should consider a rapid taper approach for patients with cancer who exhibit repeated signs of opioid misuse, an expert said. Tapering treatment with opioids for cancer-related pain can be a ...
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