FDA accepts Pharvaris NDA for oral hereditary angioedema treatment
Swiss biotech Pharvaris (Nasdaq: PHVS) has moved a step closer to the US market after the Food and Drug Administration (FDA) accepted its New Drug Application for deucrictibant immediate-release capsules as an on-demand treatment for hereditary angioedema (HAE) attacks.
The FDA has set a Prescription Drug User Fee Act target action date of April 23, 2027.
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