Pharvaris N.V. (PHVS) Stock Price & How to Invest
Last updated October 2026
Short answer
PHVS is Pharvaris N.V., a Nasdaq-listed clinical-stage biotech built almost entirely around one molecule: deucrictibant, an oral bradykinin B2 receptor antagonist for hereditary angioedema. Exposure to it is a bet on a single drug clearing FDA review (PDUFA target action date April 23, 2027 for attack treatment) and on a second filing for prevention planned for the first half of 2027 after positive Phase 3 data in September 2026, not on any current product revenue.
PHVS stock price
As of 2026-11-05, Pharvaris N.V. (PHVS) last closed at $32.53, up 49.2% over the past year. Over the past 52 weeks it has traded between $21.59 and $38.86.
Prices are daily closing prices from Yahoo Finance and may be delayed. For the live quote, check your broker or Pharvaris N.V.'s investor relations page. Walnut is informational, not investment advice.
What does Pharvaris N.V. (PHVS) do?
Pharvaris N.V. is a Dutch biopharmaceutical company headquartered in Leiden and listed on Nasdaq as PHVS. It works on one disease: hereditary angioedema (HAE), a rare genetic condition in which uncontrolled bradykinin signaling causes sudden, unpredictable and sometimes life-threatening swelling attacks. Its lead candidate, deucrictibant, is a small-molecule oral bradykinin B2 receptor antagonist developed in two formulations from the same molecule: an immediate-release (IR) capsule for treating attacks as they happen, and an extended-release (XR) tablet for preventing them. The company has no approved products and therefore no product revenue, so the income statement is essentially research spending funded by equity raises.
The investment picture rests on data and dates rather than sales. The registrational Phase 3 RAPIDe-3 study of deucrictibant IR met its primary endpoint and all eleven secondary endpoints, with median onset of symptom relief around 1.28 hours and median complete attack resolution around 11.95 hours; the results were published in The Lancet in October 2026. The FDA accepted the resulting New Drug Application in July 2026 and set a PDUFA target action date of April 23, 2027, which would make deucrictibant the first oral bradykinin B2 receptor antagonist cleared for HAE attacks. On September 8, 2026 Pharvaris reported topline data from CHAPTER-3, the registrational Phase 3 study of deucrictibant XR for prophylaxis: once-daily 40 mg dosing cut investigator-confirmed attacks by ~83% versus placebo over 24 weeks, all secondary endpoints were statistically significant, and no treatment-related serious adverse events were reported. A prevention NDA is planned for the first half of 2027.
Cash and equivalents stood at roughly 318 million euros at June 30, 2026, after a follow-on offering of roughly 132 million dollars, and the stated runway extends into 2028. The second-quarter net loss was ~47.8 million euros. As of October 16, 2026 the shares closed at ~$28.32, up ~7% year to date and ~30% over one year but down ~22% over the past month, for a market capitalization near ~$2.0 billion. Several insiders sold shares in September. A meaningful probability of approval and commercial uptake is already reflected in the price.
What's driving Pharvaris N.V. (PHVS)?
1. The deucrictibant IR filing under FDA review.
The NDA for the 20 mg immediate-release capsule was accepted in July 2026 with a PDUFA target action date of April 23, 2027, and the registrational RAPIDe-3 data were published in The Lancet in October 2026. Approval would give Pharvaris its first commercial product and, by its own description, the first oral bradykinin B2 receptor antagonist for HAE attacks. Everything about the company's transition from research spender to revenue generator runs through this date; analysts' 2027 estimates assume ~$32 million of first-year revenue.
2. CHAPTER-3 prophylaxis data and a second filing.
CHAPTER-3, the registrational double-blind Phase 3 study of deucrictibant XR for preventing attacks, read out on September 8, 2026. Among 85 participants, 40 mg once daily reduced attack rates by ~83% versus placebo (95% CI 72% to 90%), with an ~87% reduction in the Type 1 and Type 2 HAE subgroup, and all secondary endpoints were statistically significant. Treatment-emergent adverse events were more common on drug (~76% vs ~57%), though none of the serious events was judged treatment related. Prophylaxis is the larger and stickier half of the HAE market, and Pharvaris plans to file a prevention NDA in the first half of 2027, with the CHAPTER-4 extension supplying longer-term data.
3. One molecule addressing both halves of the market.
Most HAE companies own either an on-demand product or a prophylactic, and a patient typically needs both. Pharvaris is pursuing both indications with the same active compound in two formulations, and now has positive registrational data in each, which keeps manufacturing and safety work concentrated and creates the possibility of a single-brand franchise. It also means both indications share the same molecular risk: a safety or regulatory problem with deucrictibant affects everything at once.
4. A funded balance sheet ahead of the catalysts.
Cash and equivalents of roughly 318 million euros at the end of June 2026, after a follow-on offering of roughly 132 million dollars, support a runway guided into 2028. That covers the PDUFA date, the prevention filing and the initial commercial build without an obvious forced raise. Pre-commercial biotechs frequently raise into strength anyway, so further dilution ahead of a launch would not be unusual.
What are the risks to Pharvaris N.V. (PHVS)?
The concentration risk is close to total: essentially all of the value sits in one molecule, and a complete response letter, a manufacturing or inspection issue, or a safety signal in longer follow-up would hit both indications at once. CHAPTER-3 showed a higher rate of treatment-emergent adverse events on drug than on placebo, which regulators and prescribers will weigh against the efficacy. The on-demand oral niche is no longer empty, since KalVista's sebetralstat (Ekterly) reached the market first, so deucrictibant IR would arrive as a second oral entrant needing to prove differentiation on speed, dosing or tolerability rather than on novelty alone. Prophylaxis is more crowded still, with BioCryst's oral Orladeyo, Takeda's Takhzyro, CSL's garadacimab and Ionis's donidalorsen already competing, and longer-acting and one-time gene-editing approaches in development behind them. The company is pre-revenue, with a quarterly net loss near ~48 million euros and a trailing net loss of ~171 million, so continued access to equity markets remains part of the model. Finally, even after the October pullback the shares price in a good outcome, which tends to make disappointing news asymmetric.
What is the Pharvaris N.V. (PHVS) forecast?
14 analysts publish price targets on PHVS, averaging $57.69 against a $33.61 price as of November 2026, or +71.6%. The published targets run from $41.04 to $79.06, a moderate spread, and the ratings split 14 buy, 0 hold, 0 sell. Over the last six months there have been 9 raises and 0 cuts among the published actions. A price target is what an analyst published on a date, not a prediction, and sell-side ratings skew positive across the whole market.
Read the full PHVS forecast and price target for the target table, the recent rating actions by firm, and how the consensus has shifted.
Is PHVS a buy or a sell?
We give no verdict on Pharvaris N.V.. Both cases are real, which is why the question is contested at all, so here is the strongest version of each.
The case for buying. The deucrictibant IR filing under FDA review. The NDA for the 20 mg immediate-release capsule was accepted in July 2026 with a PDUFA target action date of April 23, 2027, and the registrational RAPIDe-3 data were published in The Lancet in October 2026. The most optimistic published target, $79.06, assumes this works close to its best case.
The case against. The concentration risk is close to total: essentially all of the value sits in one molecule, and a complete response letter, a manufacturing or inspection issue, or a safety signal in longer follow-up would hit both indications at once. The most pessimistic target, $41.04, is roughly what PHVS is worth if this bites instead.
Read the full bull and bear case on PHVS, including what would have to change to break either one. Walnut is not an investment adviser.
Has Pharvaris N.V. (PHVS) split its stock?
No. Pharvaris N.V. (PHVS) has not split its stock in the last 10 years. That is a statement about the window we check rather than about the company’s entire history, so an older split is possible. It also matters less than it once did: fractional shares mean a high price per share no longer keeps smaller investors out, which removed most of the practical reason to split.
How is Pharvaris N.V. (PHVS) valued? (approximate, October 2026)
A simple financial snapshot. These are approximations and refresh quarterly; for current figures see Pharvaris N.V.'s investor relations page or your broker.
- Product revenue: None. No approved products yet
- Cash and equivalents: ~318 million euros at June 30, 2026, essentially no debt
- Net loss: ~47.8 million euros in Q2 2026 (~0.70 per share); ~171 million trailing twelve months
- Free cash flow (TTM): ~-90 million
- Market cap: ~$2.0 billion (shares ~$28.32 on October 16, 2026)
- Cash runway: Guided into 2028
There is no revenue multiple to work with here, because there is no revenue: the valuation is a discounted view of what deucrictibant might sell if approved in both on-demand and prophylactic HAE. The financial statements are reported in euros while the shares trade in dollars, so the cash figure and the market cap are not directly comparable without converting. The 14 covering analysts carry a mean target near ~$58, roughly double the October 16 close, and third-quarter results are expected around mid-November 2026.
Who competes with Pharvaris N.V. (PHVS)?
Oral on-demand HAE treatments
KalVista Pharmaceuticals is the direct comparison, having brought sebetralstat (Ekterly) to market as the first oral on-demand HAE therapy in 2025. Deucrictibant IR would be the second oral option in that setting and works through a different mechanism (bradykinin B2 receptor blockade rather than plasma kallikrein inhibition), so the commercial argument turns on speed of relief, dosing convenience and payer positioning.
Long-term HAE prophylaxis
BioCryst's oral Orladeyo (berotralstat), Takeda's injectable Takhzyro (lanadelumab), CSL's garadacimab (Andembry) and Ionis's donidalorsen (Dawnzera) already share the prevention market, with Astria's navenibart and Intellia's one-time CRISPR candidate NTLA-2002 in later-stage development. Deucrictibant XR, now with positive registrational data, would enter against incumbents with sales forces and formulary positions already in place; Orladeyo is the closest comparison as the other once-daily oral preventive.
Established injectable HAE franchises
Takeda, CSL Behring and Pharming built the modern HAE market with injected and infused products such as Firazyr (icatibant, itself a bradykinin B2 antagonist), Berinert, Haegarda and Ruconest. They are less a technology threat than a distribution and pricing one: they own the prescriber relationships an oral newcomer has to displace, and icatibant is available generically at low cost.
What stocks are similar to Pharvaris N.V. (PHVS)?
Other names that sit close to PHVS: same theme, named as a direct competitor, or held beside it in the same funds. Each entry says which. Worth a look if you are thinking about diversification within a thesis rather than concentration on one ticker.
How to invest in Pharvaris N.V. (PHVS)
There are three common ways to get PHVS exposure. Buy shares (or fractional shares) directly at any major broker. Hold an ETF that includes it, which spreads the position across many companies. Or build it into a focused thematic portfolio, so PHVS sits alongside other stocks that express the same thesis.
Walnut takes the portfolio route. Describe a thesis where PHVS fits (for example “AI infrastructure” or “dividend-growth large-caps”) and the AI proposes 5 to 6 constituents with target weights. You review the plan and fund it through your own broker when you're ready.
New to this? Start with how to invest in stocks, see how to analyze a stock with AI, or compare the best AI stock analyzers.
The bottom line on Pharvaris N.V. (PHVS)
PHVS is a one-molecule, two-market hereditary angioedema story with positive Phase 3 data now in hand for both treatment and prevention and a balance sheet funded into 2028, so what is left to resolve is regulatory and commercial execution rather than whether the science works. As of mid-October 2026 the market values it near ~$2.0 billion, after a ~22% pullback over the past month.
More on Pharvaris N.V. (PHVS)
Whether PHVS is worth buying today depends more on your time horizon and what you already hold than on any single call. We walk through valuation, what would have to go right, and the risks in is PHVS a buy or a sell?, and where the stock could go from here in the PHVS stock forecast.
For income investors, whether PHVS pays a dividend and how the payout looks is covered in does PHVS pay a dividend? And to weigh PHVS against a peer, read the full side-by-side comparisons: PHVS vs HAE and PHVS vs IR.
Wondering how PHVS fits the portfolio you already own? Walnut is an AI investing app that connects your brokerage read-only and answers questions like that about your actual holdings: overlap, concentration, and how each position tracks the S&P 500. Compare the best AI portfolio analyzers or see the best AI investing apps in 2026.
Investing in Pharvaris N.V. with AI
Connect the broker you already use and ask Walnut's AI how PHVS fits what you actually hold: whether you own it already through a fund, what it would do to your concentration, and how it has tracked the S&P 500. Read-only by default, and you approve anything before it reaches your broker.
FAQ
What does Pharvaris actually do?
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Pharvaris is a clinical-stage biopharmaceutical company in Leiden, the Netherlands, listed on Nasdaq as PHVS. It develops deucrictibant, an oral small-molecule bradykinin B2 receptor antagonist, for hereditary angioedema. It has no marketed products and no product revenue as of October 2026.
What is hereditary angioedema and why does the mechanism matter?
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Hereditary angioedema is a rare inherited disorder in which excess bradykinin causes sudden swelling of the skin, gut or airway. Blocking the bradykinin B2 receptor stops the signal at the final step, which is how the injectable drug icatibant works. Deucrictibant applies that mechanism in an oral pill, which is the practical difference patients would notice.
What is the difference between deucrictibant IR and XR?
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They are two formulations of the same molecule aimed at two jobs. The immediate-release (IR) capsule is for on-demand treatment, taken when an attack starts. The extended-release (XR) tablet is for prophylaxis, taken once daily to prevent attacks from happening.
Where does the FDA review stand?
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The FDA accepted the New Drug Application for the deucrictibant IR 20 mg capsule in July 2026 and set a PDUFA target action date of April 23, 2027. Acceptance means the filing was complete enough to review, not that approval is assured. A PDUFA date is a goal for FDA action and can slip. A separate NDA for the XR prevention tablet is planned for the first half of 2027.
What did the Phase 3 data show?
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The registrational RAPIDe-3 study of deucrictibant IR met its primary endpoint and all eleven secondary endpoints, with median onset of symptom relief around 1.28 hours and median complete attack resolution around 11.95 hours; it was published in The Lancet in October 2026. The registrational CHAPTER-3 prevention study, reported September 8, 2026, showed an ~83% reduction in attack rate versus placebo with all secondary endpoints statistically significant.
What is the next catalyst?
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The CHAPTER-3 prophylaxis readout, previously the next catalyst, arrived on September 8, 2026 and was positive. What remains is the FDA action on deucrictibant IR by April 23, 2027, the prevention NDA submission planned for the first half of 2027, longer-term data from the CHAPTER-4 extension, and third-quarter financial results around mid-November 2026.
Does Pharvaris have enough cash?
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Cash and equivalents were roughly 318 million euros at June 30, 2026, after a follow-on offering of roughly 132 million dollars, with essentially no debt. Management has guided runway into 2028, which spans the PDUFA date and the planned prevention filing. Quarterly losses of roughly 45-48 million euros are the main draw on that cash.
How risky is a stock like this compared with a large-cap pharma?
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Considerably more so. A single-asset clinical-stage biotech has no revenue to cushion bad news, its value moves in steps around trial and regulatory dates rather than gradually, and a negative outcome can reprice the shares severely in one session. Position sizing and time horizon matter more here than with a diversified pharmaceutical company. Walnut is not an investment adviser and none of this is a recommendation.
What did the CHAPTER-3 prevention trial show?
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CHAPTER-3 was a 24-week, double-blind, placebo-controlled Phase 3 study in 85 people with HAE, 55 on 40 mg of deucrictibant XR once daily and 30 on placebo. The drug cut investigator-confirmed attacks per four weeks by ~83% versus placebo (95% CI 72% to 90%, p below 0.0001), with reductions visible in the first week. Treatment-emergent adverse events occurred in ~76% on drug versus ~57% on placebo, and no treatment-related serious adverse events were reported.
How has PHVS stock performed in 2026?
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As of October 16, 2026, PHVS closed at ~$28.32, up ~6.9% year to date and ~29.6% over the past year, within a 52-week range of ~$20.65 to ~$43.25. The shares fell ~22% over the past month despite the positive CHAPTER-3 data and the Lancet publication, a period that also included several insider share sales in September.
Walnut is informational, not investment advice. Financial figures on this page are approximations; always verify current numbers with Pharvaris N.V.'s investor relations page or your broker before making investment decisions.