Pharvaris

Pharvaris

Bringing an oral bradykinin b2 receptor antagonist to patients.

HQ location
Leiden, Netherlands
Launch date
Employees
Market cap
$1.5b
Enterprise value
$1.3b
Share price
$22.84 PHVS
Company register number
64239411
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DateInvestorsAmountRound
investor investor

€0.0

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€0.0

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€0.0

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N/A

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Valuation: €0.0

-9.7x EV/EBITDA

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€0.0

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investor

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$175m

Post IPO Equity
Total Funding000k

Financials

Estimates*

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Revenues, earnings & profits over time
EUR2021202220232024202520262027
Revenues0000000000000000000000000000
% growth------3250 %
EBITDA0000000000000000000000000000
% EBITDA margin-----(14362 %)(352 %)
Profit0000000000000000000000000000
% profit margin-----(13997 %)(352 %)
EV0000000000000000000000000000
EV / revenue00.0x00.0x00.0x00.0x00.0x00.0x00.0x
EV / EBITDA00.0x00.0x00.0x00.0x00.0x00.0x00.0x
R&D budget0000000000000000000000000000

Source: Company filings or news article, Equity research estimates

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More about Pharvaris
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Pharvaris is a clinical-stage biopharmaceutical company dedicated to the discovery and development of novel oral bradykinin B2 receptor antagonists. These antagonists are designed to treat hereditary angioedema (HAE) and other conditions mediated by the bradykinin B2 receptor. The company aims to provide an alternative to the currently available injected therapies, offering patients a more convenient oral treatment option. Pharvaris operates in the biopharmaceutical market, targeting patients suffering from rare and debilitating conditions. The company's business model revolves around the research, development, and eventual commercialization of its proprietary oral therapies. Revenue generation is anticipated through the successful development and approval of these therapies, followed by their marketing and sales. Pharvaris serves a niche market of patients with specific medical needs, focusing on innovative solutions that improve patient choice and quality of life.

Keywords: bradykinin B2 receptor, hereditary angioedema, oral therapy, clinical-stage, biopharmaceutical, novel antagonists, patient choice, rare diseases, alternative treatment, drug development.

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