• Incidence of Severe OM (WHO Grade ≥ 3) experienced during radiation therapy (across 7 weeks) by patients with Head and Neck Cancer receiving a cumulative radiation dose of at least 55 Gy in the course of their chemoradiation treatment • Safety and Tolerability of Brilacidin
A Secondary Endpoint included in the Interim Analysis is:
Daub... To be certain follow-ups do extend out. My comment was that dosing would conclude September 23 based on the criteria laid out in the trial protocol. I view that is an important time with BP monitoring so closely. Also, as I recall the trial was set up to administer to 60 patients. By this mornings PR 61 patients will be administered Brilacidin. Another very good sign!