<img src="https://ml.globenewswire.com/Resource/Download/4f758956-d75c-4020-9df0-b14d01115a1b?size=2" nborder="0" align="left" hspace="5" vspace="5" title="Pharvaris Logo.png" alt="Pharvaris N.V."/>ZUG, Switzerland, May 29, 2026 (GLOBE NEWSWIRE) -- <a href="https://www.globenewswire.com/Tracker?data=uIICqmiceZmFaQX1lirebCTPG7oe4vBjVy6xsIVLfDceobJgpZ_tY7mx78nL7PsRmk8WdVi9-ix9SzVxw-X1frJvdx_LOCuk2fnjsuvlCvyO2XymsAlcknAjCGxvSaHUbZ-huIwi0S-0BYQ5J1BGlQYauaL6v1pt5gQrWrljdQ8YYohhEm3oI2ZuriraAvLvrpc3F3-4wiEPgQhmBUrQpkNfui_7ZmVJ5l0GZqYwNtM=" rel="nofollow" target="_blank" title="Pharvaris">Pharvaris</a> (Nasdaq: PHVS), a late-stage biopharmaceutical company developing novel, oral bradykinin B2 receptor antagonists to help address unmet needs of those living with bradykinin-mediated diseases such as hereditary angioedema (HAE) and acquired angioedema due to C1 inhibitor deficiency (AAE-C1INH), today announced the acceptance of one abstract for oral presentation and seven abstracts for flash talk/poster presentation at the <a href="https://www.globenewswire.com/Tracker?data=lm_YVmdku5pPvI66FD6HYXGylyCubakQhurTS0-YHtJa87MrrSOYZCdwdzyrcb2pLoMsQygoOhnXH6HJVD9bGSjf8Keg1d2-ZuVbz0jpbi0uS3Jo-QTzfzXw9oA5OvxgidVqFE3n-ipr7525CyMHukQwmLEppiFZ0QPuERvB8ewMm2LzpRJAaceAlXtkXTFtqpRssyk8XcHsQ2hqSpqzvAeCAa46evF_3A42u9XrgoQ=" rel="nofollow" target="_blank" title="European Academy of Allergy and Clinical Immunology (EAACI) Annual Congress 2026">European Academy of Allergy and Clinical Immunology (EAACI) Annual Congress 2026</a>, to be held from June 12-15, 2026, in Istanbul, Turkey. Details of the presentations are as follows: <ul type="disc"><li>Title: Oral Deucrictibant Immediate-Release Capsule for On-Demand Treatment of Hereditary Angioedema Attacks: End of Progression Results in the Phase 3 RAPIDe-3 Trial Presenter: Mauro Cancian, M.D., Ph.D. Format: Oral Presentation Date, time: Friday, June 12, 2026, 3:00-4:30 p.m. TRT (8:00-9:30 a.m. EDT)</li></ul> <ul type="disc"><li>Title: Clinical Cardiovascular Safety Assessment of Oral Deucrictibant Presenter: Anne Lesage, Ph.D. Format: Poster Presentation Date, time: Friday, June 12, 2026, 12:00-1:00 p.m. TRT (5:00-6:00 a.m. EDT)</li></ul> <ul type="disc"><li>Title: A Clinically Validated Kinin Biomarker Assay to Differentiate Bradykinin-Mediated from Mast Cell-Mediated Angioedema Presenter: Evangelia Pardali, Ph.D. Format: Poster Presentation Date, time: Friday, June 12, 2026, 12:00-1:00 p.m. TRT (5:00-6:00 a.m. EDT)</li></ul> <ul type="disc"><li>Title: Evaluations of Safety Margins and Response to Deucrictibant Extended-Release (XR) Tablet in Combination with Deucrictibant Immediate-Release (IR) Capsule Presenter: Anne Lesage, Ph.D. Format: Poster Presentation Date, time: Saturday, June 13, 2026, 12:00-1:00 p.m. TRT (5:00-6:00 a.m. EDT)</li></ul> <ul type="disc"><li>Title: Oral Deucrictibant Immediate-Release Capsule for On-Demand Treatment of Hereditary Angioedema Attacks: Results of the Phase 3 RAPIDe-3 Trial Presenter: Philip Li, M.D., FRCP Format: Poster Presentation Date, time: Saturday, June 13, 2026, 12:00-1:00 p.m. TRT (5:00-6:00 a.m. EDT)</li></ul> <ul type="disc"><li>Title: RAPIDe-3 Patient Voices: Qualitative Insights from the Phase 3 Study of Oral Deucrictibant for On-Demand Treatment of Hereditary Angioedema Attacks Presenter: Anna Valerieva, M.D., Ph.D. Format: Poster Presentation Date, time: Saturday, June 13, 2026, 12:00-1:00 p.m. TRT (5:00-6:00 a.m. EDT)</li></ul> <ul type="disc"><li>Title: Results of the Phase 2 CHAPTER-1 Open-Label Extension Study on the Long-Term Safety and Efficacy of Oral Deucrictibant for Prophylaxis in Hereditary Angioedema Presenter: Markus Magerl, M.D. Format: Flash Talk Date, time: Saturday, June 13, 2026, 3:00-4:30 p.m. TRT (8:00-9:30 a.m. EDT)</li></ul> <ul type="disc"><li>Title: CHAPTER-1 Open-Label Extension Study: Long-Term Prophylactic Treatment with Oral Deucrictibant Improved Disease Control and Health-Related Quality of Life in Participants with Hereditary Angioedema Presenter: Markus Magerl, M.D. Format: Flash Talk Date, time: Saturday, June 13, 2026, 3:00-4:30 p.m. TRT (8:00-9:30 a.m. EDT)</li></ul> The posters and presentation slides will be made available on the Investors section of the Pharvaris website at the beginning of the respective presentations at: <a href="https://www.globenewswire.com/Tracker?data=K1zZuEzVB8_fMQIQw0W-HTxJEBf-wDYOomXV0znZktGZW_ea9Fdi66FSaOqLbgbRioJy2qY9beaoR5wA0-_lsb6aEHno1nhVeK46_sR9TCgCysvnMeoaAccxO5xmLs9FVTOb_rbUi6Uigvr5EG_ZMxW9C7aPcQxnhvAyB3cPqDMWgO2VX_0Lrk-XBdNGTa1j" rel="nofollow" target="_blank" title="ir.pharvaris.com/news-events/events-presentations">ir.pharvaris.com/news-events/events-presentations</a>. About Pharvaris Pharvaris is a late-stage biopharmaceutical company developing novel, oral bradykinin B2 receptor antagonists to help address unmet needs in bradykinin-mediated conditions, including all types of bradykinin-mediated angioedema. Pharvaris’ aspiration is to offer therapies with injectable-like efficacy™, a well-tolerated profile, and the convenience of oral administration to prevent and treat bradykinin-mediated angioedema attacks. By delivering on this aspiration, Pharvaris aims to provide a new standard of care in bradykinin-mediated angioedema. Pharvaris is preparing marketing authorization applications for deucrictibant immediate-release capsule as an on-demand treatment of HAE attacks, and a global pivotal Phase 3 study of deucrictibant extended-release tablet for the prevention of HAE attacks (CHAPTER-3) is ongoing with topline data anticipated in the third quarter of 2026. In addition, CREAATE is an ongoing Phase 3 study of deucrictibant for the prophylactic and on-demand treatment of AAE-C1INH attacks. For more information, visit https://pharvaris.com/. <pre>CONTACT: Contact
Maggie Beller
Vice President, Head of Corporate and Investor Communications
maggie.beller@pharvaris.com</pre> <img alt="" src='https://ml.globenewswire.com/media/ODZhYjJjMWYtM2NlNS00NTg4LWE2MGItYjk4Y2Q2M2YyNjlmLTEyMTc1MDAtMjAyNi0wNS0yOS1lbg==/tiny/Pharvaris-N-V-.png' referrerpolicy='no-referrer-when-downgrade' />

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