FDA confirms RhoVac's application for a pre-IND meeting
RhoVac AB (publ) ("RhoVac") hereby announces that FDA (US Food and Drug Administration) has accepted RhoVac's application for a pre-IND meeting, which is focused on the clinical development program with the drug candidate RV001.RhoVac's next step in the clinical development of the drug candidate RV001 is expected to start in mid-2019. Clinical development is going to be run primarily in Europe, but part of the company's strategy is to run some of the clinical development in the US. Therefore, RhoVac has submitted an application for a pre-IND meeting with the FDA to get answers and