Pharvaris/$PHVS

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About Pharvaris

Pharvaris NV is a late-stage biopharmaceutical company which is engaged in developing novel, oral bradykinin B2 receptor antagonists to prevent and treat HAE attacks. By directly pursuing this clinically therapeutic target with novel small molecules, With positive data in both Phase 2 prophylaxis and studies in HAE, Pharvaris is developing deucrictibant. Pharvaris is currently enrolling a pivotal Phase 3 study for the treatment of HAE attacks and plans to initiate a pivotal Phase 3 study of deucrictibant for the prevention of HAE attacks. The company is also running open-label extension studies in both on-demand (RAPIDe-2) and prophylactic (CHAPTER-4) settings to collect long-term safety and efficacy data in HAE patients.
Ticker
$PHVS
Sector
Health
Primary listing
NASDAQ
Employees
148
Headquarters
Zug, Switzerland

Pharvaris Metrics

BasicAdvanced
$2.7B
-
-$3.01
-2.33
-

What the Analysts think about Pharvaris

Analyst ratings (Buy, Hold, Sell) for Pharvaris stock.
Analyst projections of the future price of Pharvaris stock.

Bulls say / Bears say

CHAPTER-3 topline results announced September 8, 2026, showed an 83% reduction in HAE attack rate versus placebo, an 87% reduction in Type 1/2 HAE, statistical significance across secondary endpoints, and a well-tolerated profile—materially de-risking the prophylaxis opportunity. (sec.gov) (SEC)
The FDA accepted Pharvaris’s NDA for deucrictibant immediate-release capsules, which could make it the first oral bradykinin B2 receptor antagonist for on-demand HAE treatment; the EMA also validated the company’s marketing application in July 2026. (ir.pharvaris.com) (Pharvaris)
Liquidity is comparatively strong for a late-stage biotech: Pharvaris reported €318 million in cash and cash equivalents at June 30, 2026, and said its $132.3 million offering extends the cash runway into 2028, supporting regulatory preparation, commercial infrastructure, and ongoing pipeline work. (pharvaris.gcs-web.com) (Pharvaris)
Pharvaris remains pre-revenue and reported a €47.8 million net loss in Q2 2026, while R&D and G&A expenses increased year over year; commercialization will likely require continued substantial spending. (pharvaris.gcs-web.com) (Nasdaq)
The May 2026 equity financing raised approximately $132.3 million through 4.46 million new shares, creating near-term dilution and demonstrating that additional capital may be needed if launch costs or development spending exceed the current runway. (pharvaris.gcs-web.com) (Pharvaris)
Despite strong clinical progress, the on-demand product remains under FDA review with a PDUFA date of April 23, 2027, while the broader AAE-C1INH program is still enrolling; delays, regulatory questions, or slower market adoption could postpone revenue generation. (pharvaris.gcs-web.com) (Pharvaris)
Data summarised monthly by Lightyear AI. Last updated on 8 Sept 2026.

Pharvaris Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Pharvaris Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

Funds containing Pharvaris

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