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Pharvaris/$PHVS

1D1W1M3M6MYTD1Y5YMAX

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
$2.4B
-
-$2.92
-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

In CHAPTER-3, once-daily deucrictibant XR cut monthly HAE attacks by 83% versus placebo over 24 weeks, with all secondary endpoints met and no treatment-related serious adverse events reported. This offers a strong clinical basis for a potential oral prevention option. (Pharvaris)
In the Phase 3 RAPIDe-3 trial, oral deucrictibant brought symptom relief in a median 1.28 hours, versus more than 12 hours with placebo, and no treatment-related serious or severe adverse events were reported. The results support a potential oral option for treating attacks. (The Lancet)
The immediate-release treatment is under formal review by both the FDA and EMA, with the FDA decision targeted for April 2027. If approved, this could bring a first product closer to market while the company advances its prevention tablet. (SEC)
Deucrictibant would enter a competitive HAE market that already includes injectable prevention treatments and the oral drug Orladeyo. Newer therapies have also recently reached the market, which could make it harder to win patients and payer coverage. (Clinical Trials Arena)
Two CHAPTER-3 participants had Grade 2 liver-enzyme elevations, although Pharvaris cited possible confounding factors and said neither had symptoms or raised bilirubin. Longer-term safety data are still needed to clarify whether this will affect monitoring or uptake. (Investing.com)
Pharvaris remains pre-revenue and reported a €47.8 million net loss in the second quarter. It says its cash should fund operations into 2028, but it has relied on share offerings and says it may need further capital, leaving investors exposed to possible dilution. (SEC)
Data summarised monthly by Lightyear AI. Last updated on 1 Nov 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
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