You linked me to an accurate trial summary. The excerpt pasted below captures what I think you’re trying to say:
According to overall results, the 331-patient trial has met the primary endpoint of overall survival (OS) in newly diagnosed GBM patients after the progression-free survival (PFS) the initial primary endpoint of the trial, was found to be unviable. OS is the "gold standard" for measuring the clinical benefits of a cancer drug.
The global trial has also reached the secondary endpoint of OS in recurrent GBM with statistical significance.
OS is the "gold standard" for measuring the clinical benefits of a cancer drug. The global trial has also reached the secondary endpoint of OS in recurrent GBM with statistical significance.
In terms of safety, there were five instances of serious adverse events after the administration of 2.193 doses of DCVax-L. There were no reports of autoimmune reactions or incidences of cytokine storm, according to the presentation.