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LQDA

Liquidia Corporation

NASDAQ · USHealthcareBiotechnology
$79.90-0.05%

Price as of Jul 20, 2026

LQDA overview

Liquidia Corporation

Liquidia Corporation operates in the Healthcare sector. Its latest one-year return is +449.8%.

1-year price · 252 sessions

Valuation

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P/E forward
44.18x
EV / EBITDA
131.38x
Market cap
$7.1B

Momentum

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1 day
-0.1%
YTD
+131.8%
RSI (14d)
59.3

Summary

Liquidia Corporation (NASDAQ:LQDA) is a biopharmaceutical company founded in 2004 and headquartered in Morrisville, North Carolina. The company went public in July 2018 and focuses on developing and commercializing innovative treatments for rare diseases, particularly pulmonary arterial hypertension and pulmonary hypertension associated with interstitial lung disease. Liquidia utilizes its proprietary PRINT technology platform to create precisely engineered drug particles that can improve the delivery and efficacy of existing medications.

Over the past few years, Liquidia has executed a focused strategy centered on advancing YUTREPIA toward commercialization while expanding its pipeline. The most significant development has been navigating the complex regulatory and legal pathway for YUTREPIA approval. The company successfully amended its New Drug Application (NDA) to include both PAH and PH-ILD indications, with the FDA confirming no additional studies are required. Clinical development progress has been substantial, particularly with the ASCENT study for PH-ILD patients. This trial has demonstrated that patients can safely titrate to doses three times higher than the labeled target dose of nebulized Tyvaso, with preliminary results showing a mean 6-minute walk test improvement of 26.4 meters at week 8. The study's success supports YUTREPIA's core value proposition of superior tolerability and higher achievable therapeutic doses. The company has also significantly expanded its pipeline through the L606 program, a next-generation sustained-release liposomal treprostinil formulation designed for twice-daily dosing. The open-label safety study has shown promising results with patients reaching maximum doses of 378 micrograms with good tolerability. Liquidia plans to initiate a global Phase III RESPIRE study for L606 by year-end 2025. Commercial preparation has accelerated dramatically, with the company building a sales force of approximately 50 experienced rare disease representatives and establishing comprehensive patient support services. The team has identified roughly 6,000-7,000 potential prescriber targets and developed payer access strategies. Financially, the company strengthened its position through a $100 million financing agreement with HealthCare Royalty Partners, providing sufficient runway to achieve profitability through YUTREPIA's commercial launch without additional capital raises.

Profitability

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Gross margin
91.8%
EBIT margin
15.8%
Net margin
7.7%
ROE
20.5%
Revenue YoY
+1936.7%
EPS YoY
+115.2%
Revenue fwd
+10.8%
Revenue CAGR 3y
+115.0%

Earnings

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Latest EPS
$0.52
EPS estimate
$0.34
EPS surprise
+52.9%
Next EPS est.
$0.85

Capital & dividend

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Debt / equity
1.70x
Current ratio
2.22x
Dividend yield
Interest cover
1.75x

Financials snapshot

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Revenue · 2025
$158.3M
Net income
-$68.9M
Operating cash flow
-$35.7M

Next expected earnings · 2026-08-11T00:00:00.000Z

Latest news

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  1. Liquidia Corporation Reports First Quarter 2026 Financial Results

    Globe Newswire · 5/11/2026