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Pharvaris Says FDA Lifts Clinical Hold On Deucrictibant For On-Demand Treatment Of HAE

Pharvaris Says FDA Lifts Clinical Hold On Deucrictibant For On-Demand Treatment Of HAE

Pharvaris N.V. (PHVS) announced Monday the U.S. Food and Drug Administration (FDA) has lifted the clinical hold on the Investigational New Drug (IND) application for deucrictibant for the on-demand treatment of hereditary angioedema or HAE, following review of data from a preplanned interim analysis of the ongoing 26-week nonclinical study.
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