RhoVac receives FDA approval in the US for the start of its Phase IIb clinical trial
RhoVac AB ("RhoVac") announces today, February 28[th] 2020, that the US Food and Drug Administration (FDA) has approved RhoVac to initiate its clinical phase IIb study in prostate cancer in the United States, and the FDA has thus accepted the company's Investigational New Drug (IND) application. The study, titled RhoVac-002 ("BRaVac") is an international multicenter study, which is expected to recruit at least 175 patients in the EU as well as in the United States. RhoVac has previously received approval for the start of the clinical phase IIb trial in Denmark, Finland, Germany and Belgium.