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Pharvaris (PHVS)

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Research analysts covering Pharvaris.

Recent press releases and 8-K filings for PHVS.

Pharvaris Details Positive Phase III On-Demand Data and Prophylactic Outlook for Deucrictibant
PHVS
Product Launch
New Projects/Investments
Guidance Update
  • Pharvaris reported positive Phase III RAPIDe-3 data for its HAE treatment, deucrictibant, in the on-demand setting, demonstrating onset of symptom relief in 1.28 hours and end of progression in 17 minutes.
  • The company plans to file its New Drug Application (NDA) for on-demand deucrictibant in the first half of 2026, with a potential launch approximately one year thereafter, subject to regulatory review.
  • Phase III data for deucrictibant in the prophylactic setting is expected in Q3 2026. Prior Phase II data indicated 84.5% attack reduction, aligning with injectable therapies.
  • Pharvaris will present six posters at the AAAAI conference, including the first public presentation of RAPIDe-3 Phase III top-line data and final data from the CHAPTER-1 open-label extension, which showed a 92.3% attack reduction in the prophylactic setting.
  • The company projects its cash runway to extend into the first half of 2027.
Feb 26, 2026, 2:20 PM
Pharvaris Provides Update on Deucrictibant Clinical Trials and Financial Outlook
PHVS
Product Launch
Guidance Update
  • Pharvaris reported positive Phase 3 data for deucrictibant in the on-demand setting (RAPIDe-3), demonstrating rapid onset of symptom relief and complete attack resolution.
  • The company plans to file its NDA for on-demand deucrictibant in the first half of 2026, with a potential launch approximately one year later.
  • Phase 3 data for prophylactic deucrictibant (extended-release version) is anticipated in Q3 2026, following Phase 2 results that showed 84.5% attack reduction, comparable to injectable therapies.
  • Pharvaris expects its current cash on hand to provide a runway into the first half of 2027.
Feb 26, 2026, 2:20 PM
Pharvaris Updates on Deucrictibant HAE Program and Financial Runway
PHVS
Guidance Update
Product Launch
New Projects/Investments
  • Pharvaris reported positive Phase 3 data for deucrictibant in the on-demand setting for HAE, demonstrating rapid symptom relief with onset in 1.28 hours and end of progression in 17 minutes.
  • The company plans to file its New Drug Application (NDA) for on-demand deucrictibant in H1 2026, with a potential launch approximately one year later.
  • Phase 3 data for deucrictibant in the prophylactic setting is expected in Q3 2026, following Phase 2 results that showed 84.5% attack reduction, aligning with injectable therapies (80-87%) and surpassing existing oral options (44%).
  • Deucrictibant differentiates from a recently launched oral competitor (EKTERLY) with a higher single-dose resolution rate (83% vs. 59%) and a small softgel capsule formulation.
  • Pharvaris anticipates its current cash on hand will provide a financial runway into the first half of 2027.
Feb 26, 2026, 2:20 PM
Pharvaris Outlines 2026 Strategic Priorities and Clinical Development Milestones
PHVS
New Projects/Investments
Guidance Update
Product Launch
  • Pharvaris anticipates topline data from its pivotal Phase 3 CHAPTER-3 study for the prophylactic treatment of HAE attacks in the third quarter of 2026.
  • The company is on track to file the New Drug Application (NDA) for deucrictibant for the on-demand treatment of HAE attacks in the first half of 2026.
  • Recruitment is ongoing in the pivotal Phase 3 CREAATE study for deucrictibant in AAE-C1INH attacks.
  • Pharvaris reported approximately €329 million in cash and cash equivalents as of September 30, 2025, providing an estimated cash runway into the first half of 2027.
Jan 12, 2026, 11:51 AM
Pharvaris Announces Positive Phase 3 RAPID-3 Study Results for Deucrictibant
PHVS
Product Launch
New Projects/Investments
Guidance Update
  • Pharvaris announced positive top-line results from its RAPID-3 pivotal Phase 3 study of deucrictibant for the on-demand treatment of Hereditary Angioedema (HAE) attacks, meeting its primary endpoint and all secondary efficacy endpoints.
  • Deucrictibant demonstrated a significantly faster onset of symptom relief with a median time of 1.28 hours compared to greater than 12 hours for placebo, and was well tolerated with no safety signals identified.
  • The company aims to file for global marketing authorization for deucrictibant in the on-demand treatment of HAE attacks in the first half of 2026.
  • Pharvaris is also developing an extended-release tablet of deucrictibant for prophylaxis, with results from the CHAPTER-3 study anticipated in the second half of 2026.
Dec 3, 2025, 1:00 PM
Pharvaris Announces Positive Topline Data from RAPIDe-3 Study for Deucrictibant
PHVS
Product Launch
  • Pharvaris announced positive topline results from the RAPIDe-3 Phase III clinical study of deucrictibant immediate release capsule for the on-demand treatment of hereditary angioedema (HAE) attacks.
  • Deucrictibant achieved the primary endpoint with a median time to onset of symptom relief of 1.28 hours, significantly faster than placebo (not estimable). Key secondary endpoints also showed strong efficacy, including end-of-progression within 17.5 minutes and substantial symptom relief within 2.85 hours.
  • The treatment was very well tolerated, with most adverse events being mild or moderate and no safety signals identified.
  • Pharvaris aims to submit a first global marketing authorization for deucrictibant for on-demand HAE treatment in the first half of 2026.
Dec 3, 2025, 1:00 PM
Pharvaris Announces Positive Topline Data from RAPID-3 Phase III Study for Deucrictibant
PHVS
Product Launch
New Projects/Investments
  • Pharvaris announced positive topline data from its Phase III RAPID-3 clinical study of deucrictibant Immediate Release Capsule for the on-demand treatment of hereditary angioedema (HAE) attacks.
  • Deucrictibant demonstrated a significantly faster onset of symptom relief with a median time of 1.28 hours, compared to "not estimable" (beyond 12 hours) for placebo.
  • Approximately 85% of deucrictibant-treated attacks achieved onset of symptom relief by the four-hour mark, versus around 30% for placebo-treated attacks.
  • The drug was very well tolerated, with most adverse events being mild or moderate, and no safety signals identified.
  • Pharvaris plans to pursue global marketing authorization for deucrictibant for on-demand HAE treatment, with results from the prophylactic CHAPTER-3 study expected in the second half of next year.
Dec 3, 2025, 1:00 PM
PHVS Provides Update on Deucrictibant Clinical Study Results and Regulatory Timeline
PHVS
New Projects/Investments
Product Launch
Guidance Update
  • Deucrictibant demonstrated significantly faster onset of symptom relief in 1.28 hours compared to placebo, where the median time was not estimable within 12 hours.
  • The treatment also showed a faster End of Progression (EoP) in 17.47 minutes and earlier complete symptom resolution in 11.95 hours compared to placebo.
  • 83.0% of attacks were treated with a single capsule of deucrictibant (vs. 33.0% for placebo), and 93.2% of attacks were treated without rescue medication (vs. 63.6% for placebo), with the treatment being well tolerated and no discontinuations due to treatment-emergent adverse events (TEAEs).
  • Pharvaris plans to file a New Drug Application (NDA) for deucrictibant for Hereditary Angioedema (HAE) On-Demand in the first half of 2026.
Dec 3, 2025, 1:00 PM
Pharvaris Announces Positive Topline Data from RAPIDe-3 Pivotal Study
PHVS
Product Launch
New Projects/Investments
  • On December 3, 2025, Pharvaris N.V. announced positive topline data from its RAPIDe-3 pivotal study for deucrictibant, an oral treatment for hereditary angioedema (HAE) attacks.
  • The study met its primary endpoint, demonstrating a median time to onset of symptom relief of 1.28 hours, significantly faster than placebo (p<0.0001).
  • All secondary efficacy endpoints were also met, including a median time to End of Progression of 17.47 minutes and complete symptom resolution in 11.95 hours.
  • Deucrictibant exhibited a well-tolerated safety profile with no treatment-related serious adverse events.
  • Pharvaris plans to submit marketing authorization applications, including a New Drug Application (NDA) with the U.S. FDA, for deucrictibant in the first half of 2026.
Dec 3, 2025, 11:56 AM
Pharvaris Reports Q3 2025 Financial Results and Provides Business Update
PHVS
Earnings
Guidance Update
New Projects/Investments
  • Pharvaris reported cash and cash equivalents of €329 million as of September 30, 2025, following a public offering in July 2025 that generated net proceeds of approximately €160.3 million, extending the company's cash runway well into the first half of 2027.
  • The company anticipates topline data for the RAPIDe-3 pivotal Phase 3 study in 4Q2025 and for the CHAPTER-3 pivotal Phase 3 study in 2H2026.
  • For the third quarter ended September 30, 2025, Pharvaris reported a net loss of €37.1 million and basic and diluted loss per share of €0.60.
  • Research and development expenses increased to €29.8 million in Q3 2025 from €25.8 million in Q3 2024, while general and administrative expenses decreased to €9.8 million from €12.1 million over the same period.
Nov 12, 2025, 1:00 PM