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  • Pharvaris published Phase 3 RAPIDe-3 results for on-demand deucrictibant immediate-release therapy in The Lancet, showing HAE attack symptom relief beginning at 1.28 hours and complete resolution by 11.95 hours, with a favorable safety profile.Oct 10, 2026
  • Pharvaris' Phase 3 CHAPTER-3 trial met its primary endpoint for oral deucrictibant XR in HAE prophylaxisSep 8, 2026
  • Deucrictibant data supported oral treatment of hereditary angioedemaSep 3, 2026

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News

  • Pharvaris reports publication in The Lancet of Phase 3 results demonstrating rapid and sustained efficacy of deucrictibant in treating HAE attacksOct 9, 2026
  • Pharvaris' real-world analysis of hereditary angioedema disease experience and treatment satisfaction gaps is published in Advances in TherapyOct 5, 2026
  • Pharvaris reported positive topline results from the pivotal Phase 3 CHAPTER-3 study of extended-release deucrictibant for HAE attack prophylaxisSep 8, 2026
  • Study on AAE-C1INH disease burden and clinical trial endpoint validation was published in Frontiers in ImmunologyAug 6, 2026
  • FDA accepted Pharvaris' new drug application for deucrictibant IR for on-demand treatment of hereditary angioedema attacksJul 8, 2026

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