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LQDA Overview

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$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
71.990
Open
70.440
VWAP
69.96
Vol
12.43M
Mkt Cap
6.32B
Low
66.830
Amount
869.93M
EV/EBITDA(TTM)
128.54
Total Shares
88.93M
EV
6.06B
EV/OCF(TTM)
126.29
P/S(TTM)
21.46
Liquidia Corporation is a biopharmaceutical company. The Company is engaged in the development and commercialization of therapeutic products for cardiopulmonary diseases. The Company operates within the biotechnology sector, focusing on treatments for conditions such as pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). The Company operates through its wholly owned operating subsidiaries, Liquidia Technologies, Inc. and Liquidia PAH, LLC. Its proprietary PRINT technology is a particle engineering platform, which enables precise production of uniform drug particles. Its lead product candidate is YUTREPIA for the treatment of PAH and PH-ILD. YUTREPIA is a PRINT‑engineered inhaled dry‑powder formulation of treprostinil designed to enhance deep lung delivery, improve therapeutic performance, and enable higher dose administration through a convenient inhaler.
Show More

Events Timeline

(ET)
2026-06-04
12:10:00
Liquidia Shares Rise 17.6% to $65.50
select
2026-05-11 (ET)
2026-05-11
16:30:00
Major Averages Close Slightly Higher as Investors Focus on Economic Data
select
2026-05-11
12:10:00
Major Averages Slightly Higher as Investors Eye Geopolitical Risks
select

News

NASDAQ.COM
8.5
20:03 PMNASDAQ.COM
uniQure Achieves Major Regulatory Milestone for Gene Therapy
  • Stock Surge: uniQure's shares soared 78.4% on June 17 following the announcement of a major regulatory milestone for AMT-130, although a 3.9% drop on June 18 indicates some volatility; overall, investor confidence in the therapy appears to be strengthening.
  • FDA Meeting Outcomes: During a recent Type B meeting, the FDA confirmed that three-year data from the AMT-130 study could serve as the primary basis for a Biologics License Application (BLA), which is expected to be filed in Q3 2026, potentially accelerating market access for the therapy.
  • Clinical Trial Design Adjustments: The FDA has requested that uniQure align on the confirmatory study design before BLA submission, including the consideration of a standard-of-care control group, which will impact future clinical trial strategies and timelines.
  • Significant Market Potential: As the first therapy for Huntington's disease to receive FDA's Regenerative Medicine Advanced Therapy (RMAT) designation, AMT-130's potential approval could significantly enhance uniQure's market position, addressing a substantial unmet need in Huntington's disease treatment and presenting considerable commercial opportunities for the company.
NASDAQ.COM
8.5
16:03 PMNASDAQ.COM
Beam Therapeutics Receives FDA Clearance for Gene-Editing Therapy
  • FDA Approval Milestone: Beam Therapeutics received FDA clearance for its BEAM-304 gene-editing therapy, marking a significant advancement in the liver-targeted genetic disease space, which is expected to enhance its competitiveness in the rare disease market.
  • Significant Treatment Potential: BEAM-304 aims to correct mutations in the PAH gene responsible for phenylketonuria (PKU) by lowering toxic phenylalanine levels, potentially allowing patients to maintain a normal diet and reducing reliance on specialized medical foods, which could have a profound market impact.
  • Clinical Trial Plans: Beam plans to conduct a Phase I/II open-label clinical study in PKU patients to assess the safety and tolerability of BEAM-304, which is expected to provide critical data for the clinical application of gene-editing therapies and drive future treatment options.
  • Strong Stock Performance: Year-to-date, Beam Therapeutics' stock has risen 23.2%, significantly outperforming the biotechnology sector, reflecting positive market expectations for its new therapy and increased investor confidence.
NASDAQ.COM
9.0
06-17NASDAQ.COM
Mirum and Incyte Report Positive Results for FOP Study
  • Clinical Trial Results: Mirum and Incyte's Phase II PROGRESS study of zilurgisertib showed that only 3.1% of patients developed new lesions compared to 16.7% in the placebo group, achieving an 81% reduction, indicating the drug's potential in treating this ultra-rare disease.
  • Sustained Efficacy: In the open-label extension phase, no new lesions were observed among patients continuing zilurgisertib treatment at 48 weeks, with total lesion volume continuing to decline, demonstrating the drug's long-term efficacy and safety, addressing the urgent need for effective treatments.
  • FDA Priority Review: Following positive clinical data, the FDA has accepted the NDA for zilurgisertib and granted Priority Review status, with a decision expected by September 26, 2026, which will expedite the drug's market entry to meet the demand for new therapies.
  • Market Performance: Year-to-date, shares of Mirum and Incyte have risen by 28.5% and 1%, respectively, against a 1.4% decline in the biotech sector, reflecting investor optimism regarding their clinical advancements and enhancing their competitive position in the market.
NASDAQ.COM
6.0
06-12NASDAQ.COM
Liquidia Corp Stock Surpasses Analyst Target Price
  • Stock Performance: Liquidia Corp's shares recently rose to $71.72, surpassing the average analyst 12-month target price of $66.12, indicating increased market confidence and potentially attracting more investor interest.
  • Analyst Reactions: When a stock reaches its target price, analysts typically either downgrade their valuation or raise their target; currently, Liquidia's target prices range from $59.00 to $75.00, reflecting varying expectations about the company's future performance.
  • Market Signal: The stock's breach of the target price provides a strong signal for investors to reassess the company, prompting them to consider whether the current valuation is justified or if it’s time to take profits to mitigate risk.
  • Analyst Ratings: The average rating for Liquidia Corp within the Zacks coverage universe ranges from 1 to 5, with 1 being a Strong Buy and 5 a Strong Sell, highlighting the differing opinions among analysts regarding the company's future outlook.
Newsfilter
8.5
06-11Newsfilter
Liquidia Presents Research at PHA 2026 Conference
  • Research Presentation: Liquidia will present four posters at the 2026 PHA International Conference, highlighting patient-reported cough outcomes from the ASCENT study of YUTREPIA®, demonstrating the company's commitment to pulmonary hypertension patients.
  • Patient Feedback Analysis: The posters will showcase cough outcomes in patients with pulmonary hypertension associated with interstitial lung disease over 24 weeks of treatment, providing insights that could influence future treatment strategies.
  • Care Team Role Exploration: Liquidia will also discuss the role of pharmacists within pulmonary hypertension care teams and the mental health challenges faced by caregivers, aiming to enhance support for patients and their families.
  • Safety and Efficacy Data Review: The company will reiterate safety and exploratory efficacy data from the ASCENT study, further solidifying the potential application of YUTREPIA® in treating pulmonary hypertension.
Newsfilter
8.5
06-08Newsfilter
Liquidia Corporation to Join S&P SmallCap 600 Index
  • Index Inclusion Milestone: Liquidia Corporation announced its inclusion in the S&P SmallCap 600 Index effective June 22, 2026, marking a significant advancement in market capitalization, liquidity, and profitability, which is expected to enhance its visibility and attractiveness among investors.
  • Positive CEO Remarks: CEO Roger Jeffs stated that this inclusion is a testament to the team's efforts, reflecting the company's commitment to innovation and operational excellence, with a continued focus on improving care for patients with respiratory and vascular diseases.
  • Driving Technological Innovation: Liquidia has developed YUTREPIA® inhalation powder for pulmonary arterial hypertension (PAH) using its proprietary PRINT® technology, and is also developing L606, a new extended-release formulation, showcasing its innovative capabilities in the biopharmaceutical sector.
  • Market Outlook: With its inclusion in the small-cap index, Liquidia anticipates attracting more investor attention, potentially driving its market capitalization and long-term value creation, thereby strengthening its position in the highly competitive biopharmaceutical market.
Wall Street analysts forecast LQDA stock price to rise
8 Analyst Rating
Wall Street analysts forecast LQDA stock price to rise
8 Buy
0 Hold
0 Sell
Strong Buy
Current: 0.000
sliders
Low
31.00
Averages
47.50
High
67.00
Current: 0.000
sliders
Low
31.00
Averages
47.50
High
67.00
H.C. Wainwright
Buy
maintain
$67 -> $75
AI Analysis
2026-06-05
Reason
H.C. Wainwright
Price Target
$67 -> $75
AI Analysis
2026-06-05
maintain
Buy
Reason
H.C. Wainwright raised the firm's price target on Liquidia to $75 from $67 and keeps a Buy rating on the shares. The firm cites positive sentiment from the recent Supreme Court ruling going into the anticipated Judge Andrews decision for the target boost. The Supreme Court's ruling that Hikma Pharmaceuticals did not infringe patents held by Amarin has positive readthrough to Liquidia's legal case as it eliminates a "worse case scenario" of a potential forced new drug application withdrawal, the analyst tells investors in a research note.
Raymond James
Strong Buy
maintain
$68
2026-06-04
Reason
Raymond James
Price Target
$68
2026-06-04
maintain
Strong Buy
Reason
Raymond James reiterated a Strong Buy rating and $68 price target on Liquidia, with the analyst saying the firm is flagging Liquidia strength due to what it perceives to be as positive readthrough from the recent Supreme Court decision in Hikma v. Amarin. While this case is not an apples-to-apples comparison to the highly-anticipated '327 patent dispute decision, the firm does see this as generally positive readthrough for Liquidia, whose downside floor continues to rise. The firm also notes there could be a chance this means the '327 decision could be a more imminent event.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for LQDA
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Valuation Metrics

The current forward P/E ratio for Liquidia Corp (LQDA.O) is 32.79, compared to its 5-year average forward P/E of -7.43. For a more detailed relative valuation and DCF analysis to assess Liquidia Corp's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-7.43
Current PE
32.79
Overvalued PE
15.90
Undervalued PE
-30.75

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
-5.22
Current EV/EBITDA
11.16
Overvalued EV/EBITDA
8.21
Undervalued EV/EBITDA
-18.65

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
22.55
Current PS
5.21
Overvalued PS
37.94
Undervalued PS
7.15

Financials

AI Analysis
Annual
Quarterly

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Whales Holding LQDA

C
Caxton Associates (USA) LLC
Holding
LQDA
+31.38%
3M Return
B
Boothbay Fund Management, LLC
Holding
LQDA
+19.55%
3M Return
T
The Caprock Group, LLC
Holding
LQDA
+14.38%
3M Return
F
Farallon Capital Management, L.L.C.
Holding
LQDA
+12.80%
3M Return
T
TCG Crossover Management, LLC
Holding
LQDA
+7.00%
3M Return
E
Eversept Partners, L.P.
Holding
LQDA
-0.66%
3M Return

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Frequently Asked Questions

What is Liquidia Corp (LQDA) stock price today?

The current price of LQDA is 71.07 USD — it has increased 3.53

What is Liquidia Corp (LQDA)'s business?

Liquidia Corporation is a biopharmaceutical company. The Company is engaged in the development and commercialization of therapeutic products for cardiopulmonary diseases. The Company operates within the biotechnology sector, focusing on treatments for conditions such as pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). The Company operates through its wholly owned operating subsidiaries, Liquidia Technologies, Inc. and Liquidia PAH, LLC. Its proprietary PRINT technology is a particle engineering platform, which enables precise production of uniform drug particles. Its lead product candidate is YUTREPIA for the treatment of PAH and PH-ILD. YUTREPIA is a PRINT‑engineered inhaled dry‑powder formulation of treprostinil designed to enhance deep lung delivery, improve therapeutic performance, and enable higher dose administration through a convenient inhaler.

What is the price predicton of LQDA Stock?

Wall Street analysts forecast LQDA stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for LQDA is47.50 USD with a low forecast of 31.00 USD and a high forecast of 67.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Liquidia Corp (LQDA)'s revenue for the last quarter?

Liquidia Corp revenue for the last quarter amounts to 132.87M USD, increased 4158.49

What is Liquidia Corp (LQDA)'s earnings per share (EPS) for the last quarter?

Liquidia Corp. EPS for the last quarter amounts to 0.52 USD, decreased -215.56

How many employees does Liquidia Corp (LQDA). have?

Liquidia Corp (LQDA) has 216 emplpoyees as of June 19 2026.

What is Liquidia Corp (LQDA) market cap?

Today LQDA has the market capitalization of 6.32B USD.