Cantor Global Healthcare Conference 2025
Logotype for Pharvaris N.V.

Pharvaris (PHVS) Cantor Global Healthcare Conference 2025 summary

Event summary combining transcript, slides, and related documents.

Logotype for Pharvaris N.V.

Cantor Global Healthcare Conference 2025 summary

5 Jan, 2026

Company overview and development pipeline

  • Late-stage pre-commercial biotech developing a single active ingredient for both treatment and prevention of bradykinin-mediated attacks.

  • Anticipates key data readouts in Q4 this year and another phase III readout in the second half of next year.

  • Plans to file for approval in the US in the first half of 2026, targeting a launch in early 2027.

  • Preparing for commercial launch by expanding the organization and building relationships with key stakeholders.

  • Considering partnerships for ex-US commercialization due to pricing and market access challenges.

Product positioning and market landscape

  • Deucrictibant aims to be a leading oral therapy for both on-demand and prophylactic use in HAE, with injectable-like efficacy and placebo-like safety.

  • Oral therapies are expected to become the dominant first-line option for prophylaxis, with a significant share of new patients already choosing oral options.

  • The product targets four key market segments: new prophylaxis patients, patients who discontinued other oral therapies, current oral users, and injectable users.

  • Anticipates that oral therapies could capture 50–60% of the total market over time.

  • The ability to offer both on-demand and prophylactic oral therapy is seen as a major differentiator.

Clinical development and trial design

  • Phase III on-demand trial aims to confirm rapid onset of symptom relief (within 15–30 minutes) and complete resolution within 12 hours, with over 85% of attacks resolved with a single dose.

  • Trial design includes intensive assessment with 25 time points in 24 hours to capture efficacy endpoints.

  • Extended-release formulation for prophylaxis is expected to improve safety and efficacy, with higher and more persistent trough levels.

  • Real-world use in acquired angioedema patients supports confidence in the extended-release formulation.

  • Innovative endpoints, such as end of progression, are included to demonstrate rapid action.

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