Pharvaris B.V. reported Phase II data on 6 December for its oral candidate for hereditary angioedema that both it and analysts are saying suggest biologic-like efficacy with the convenience of oral therapy. The catch? Pharvaris needs to get a US Food and Drug Administration hold lifted before it can try to set up an end-of-Phase II meeting with the agency and initiate a Phase III program.
CEO Berndt Modig told a same-day investor call that Pharvaris already is in the initial planning stages for the Phase...







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