Regulatory and ethics approvals have been received for USA
** A** total of 15 sites in 7 different European countries were open for enrolment by mid-August 2019. (Norway, Germany, France, Spain, Belgium, Poland, Sweden and Denmark)
The median overall survival in the fourth dose cohort in the dose-escalation part ended at 21.7 months, with half of the patients exceeding 30 months survival including one patient still being alive more than three years after treatment.
The overall development strategy for fimaVACC is two-pronged, both utilising the current Phase I results in direct partnering efforts and plan for clinical proof-of-concept in a disease setting.
FimaVACC
Preclinical results were recently published in the high-impact immunology journal “Frontiers in
Immunology”