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Study shows oral deucrictibant quickly relieves hereditary angioedema attacks, pending FDA and EMA approval

Company Fundamentals
08 Oct 2026
GlobeNewsWire
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Bullish
Study shows oral deucrictibant quickly relieves hereditary angioedema attacks, pending FDA and EMA approval

Pharvaris announced that the Phase 3 RAPIDe-3 study results, published in The Lancet, demonstrate that oral deucrictibant provides rapid and sustained relief from hereditary angioedema (HAE) attacks, with symptom relief starting in about 1.3 hours and full resolution in under 12 hours. The drug was well tolerated and effective across various patient subgroups. Deucrictibant is under regulatory review by the FDA and EMA for on-demand HAE treatment, potentially becoming the first approved oral bradykinin B2 receptor antagonist. This advancement could offer a convenient oral option for patients who currently rely on injectable therapies.

The Phase 3 study results for deucrictibant in treating HAE attacks provide context for health sector activity on Pluang. Of 128 priced US health stocks, 51 rose and 76 fell. Notable movers include AbCellera Biologics Inc (ABCL) at USD 12.06, down 6.00%, CVS Health Corp (CVS) at USD 83.45, down 5.12%, and Immunovant Inc. (IMVT) at USD 30.43, down 5.02%. Data is as of Oct 09, 2026 03:21 WIB.

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