The Phase 1b lead-in trial, , which is enrolling up to 18 patients, is intended to identify the optimal dosage of HER-Vaxx for the study’s Phase 2, and to confirm the drug’s safety and immunogenecity. Phase 2 will involve approximately 68 patients and will be an open label study,randomised into two groups: HER-Vaxx plus standard-of-care(chemotherapy) and standard-of-care alone. The endpoints of Phase 2 will be safety, immune response, progression-free survival and overall survival.
all sounds good for moving forward
November News Letter, page-2
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