MinervaX announces that it today data have been received from the primary 3-month time point clinical endpoint of the Phase I Part B. The data supports dose-selection made based on Part A. The data further supports the vaccine is highly immunogenic already 14 days after the first dose, and that the antibodies are functionally active in killing Group B Streptococcus and preventing host-invasion.
- MinervaX provides clinical and leadership update 07/10/2021
- MinervaX announces completion of 47.4 mEUR financing 15/12/2020
- MinervaX announces investment of 4.4 mEUR 21/01/2019
- MinervaX announces results from Phase I clinical trial 05/01/2017
- Innovation Foundation Grant 19/09/2016