NOXXON Pharma: Data Safety Monitoring Board Confirms Safety and Validates Recruitment of Last Patients in Final High-Dose Cohort of NOX-A12 in Phase 1/2 Brain Cancer Study
The DSMB concluded that it is safe and appropriate to continue patient recruitment according to the study protocol.
- The DSMB concluded that it is safe and appropriate to continue patient recruitment according to the study protocol.
- The Phase 1/2 clinical study is testing three dose regimens of NOX-A12 (200, 400 and 600 mg/week), each combined with external-beam radiotherapy, in newly diagnosed brain cancer patients.
- Based on the DSMBs confirmation, participating clinical centers have now initiated final patient recruitment for the last and highest dose group.
- The outcome of this meeting will inform the recommended dose for the next randomized, controlled brain cancer trial which will lead to the registration of NOX-A12.