Pharvaris N.V. (PHVS) Stock Price & How to Invest

Last updated July 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) and in a prophylaxis readout, not in any current product revenue.

PHVS stock price

As of 2026-08-07, Pharvaris N.V. (PHVS) last closed at $34.91, up 73.5% over the past year. Over the past 52 weeks it has traded between $20.12 and $35.96.

PHVS last close
$34.91
1 day
+1.34%
1 month
-2.83%
1 year
+73.51%
52-week range
$20.12 to $35.96
Last close
2026-08-07

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 pivotal 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 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. Topline data from CHAPTER-3, the pivotal Phase 3 study of deucrictibant XR for prophylaxis, was guided for the third quarter of 2026. Cash and equivalents stood at roughly 247 million euros at March 31, 2026, and a follow-on offering of roughly 132 million dollars completed after quarter end pushed the stated runway into 2028. Against a market capitalization of roughly 2.4 billion dollars, 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. 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.

2. The CHAPTER-3 prophylaxis readout.

CHAPTER-3 is the pivotal Phase 3 study of deucrictibant XR for preventing attacks rather than treating them, with topline data guided for the third quarter of 2026. Prophylaxis is the larger and stickier half of the HAE market, since patients dose continuously rather than episodically. The open-label CHAPTER-1 extension pointed in an encouraging direction, with mean attack rate falling from about 2.18 to about 0.12 attacks per month and roughly half of participants reported attack free, but an open-label extension is not a controlled pivotal trial.

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, 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 247 million euros at the end of the first quarter of 2026, plus a follow-on offering of roughly 132 million dollars priced shortly afterwards, support a runway guided into 2028. That covers the PDUFA date 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. 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, burning roughly 30 million euros a quarter in research and development against a quarterly net loss near 39 million euros, so continued access to equity markets remains part of the model. Finally, at a market capitalization around 2.4 billion dollars the shares already 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 $48.42 against a $34.91 price as of August 2026, or +38.7%. The published targets run from $35.51 to $75.21, a wide spread, and the ratings split 13 buy, 1 hold, 0 sell. Over the last six months there have been 2 raises and 2 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. The most optimistic published target, $75.21, 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, $35.51, 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.

How is Pharvaris N.V. (PHVS) valued? (approximate, August 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: ~247 million euros at March 31, 2026, plus a ~$132 million follow-on closed after quarter end
  • R&D expense: ~30.2 million euros in Q1 2026 (vs ~30.9 million a year earlier)
  • Net loss: ~39.2 million euros in Q1 2026 (~0.60 euros per share)
  • Market cap: ~$2.4 billion (shares around $35 in early August 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. Second-quarter 2026 results were scheduled for release on August 19, 2026, after the figures above.

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 enters against incumbents with sales forces and formulary positions already in place.

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 Phase 3 data in hand and a balance sheet funded into 2028, so what is left to resolve is regulatory and commercial execution rather than whether the science works.

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 IR and PHVS vs BCRX.

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 August 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 regularly 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.

What did the Phase 3 data show?

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The pivotal RAPIDe-3 study of deucrictibant IR met its primary endpoint and all eleven secondary endpoints. Median onset of symptom relief was reported around 1.28 hours and median complete attack resolution around 11.95 hours, both well ahead of placebo. The separate open-label CHAPTER-1 extension reported mean attack rate falling from about 2.18 to about 0.12 per month.

What is the next catalyst?

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Topline data from CHAPTER-3, the pivotal Phase 3 study of deucrictibant XR for prophylaxis, was guided for the third quarter of 2026. Second-quarter 2026 financial results were scheduled for August 19, 2026. The PDUFA action date in April 2027 sits behind both.

Does Pharvaris have enough cash?

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Cash and equivalents were roughly 247 million euros at March 31, 2026, and a follow-on offering of roughly 132 million dollars closed shortly after. Management has guided runway into 2028, which spans the PDUFA date. Quarterly research and development spending of roughly 30 million euros is 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.

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.