It may differ depending on the nature of the event – e.g. related events (see below) captured for a longer period than all other events. All definitions describe the strictest requirements for ...

Neurogene (NGNE) said that a patient who had been previously identified as developing a treatment-related serious adverse event, or SAE, is now in critical condition. The patient, who had received ...

The FDA had placed the hold on the testing last month after it received a report that a patient in the Phase 2 trial had "a spontaneous report of a serious adverse event (SAE) of motor neuropathy ...

Primary endpoint met, GH001 led to an ultra-rapid anti-depressant effect with a significant placebo-adjusted MADRS reduction from baseline of ...