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Pharvaris’ Oral HAE Drug Deucrictibant Delivers Rapid Relief in Pivotal Phase 3

The company aims to file for FDA approval in the first half of 2026.

Overview

  • RAPIDe-3 met its primary endpoint with a median time to onset of symptom relief of 1.28 hours compared with more than 12 hours on placebo.
  • All secondary endpoints were achieved, including End of Progression at 17.47 minutes and complete symptom resolution at 11.95 hours.
  • Deucrictibant was well tolerated with no treatment-related serious adverse events and no discontinuations due to side effects.
  • The global study enrolled 134 participants across 24 countries and showed consistent efficacy and safety across HAE subtypes and attack severities.
  • In treated attacks, 83.0% required a single capsule and 93.2% did not need rescue medication, with an open-label extension study ongoing.